sabato 28 gennaio 2012

44_01

Treatment Selection and Technique: Vocal Cord Carcinoma

Selection of Treatment Modality

In treating vocal cord carcinoma, the goal is cure with the best functional result and the least risk of a serious complication. Patients may be considered to be in an early group if the chance of cure with larynx preservation is high, they are in a moderately advanced group if the likelihood of local control is 60% to 70% but the chance of cure is still good, and they are in an advanced group if the chance of cure is moderate and the likelihood of laryngeal preservation is relatively low. The early group may be treated initially by radiation therapy or, in selected cases, by partial laryngectomy. The moderately advanced group may be treated with either irradiation with laryngectomy reserved for relapse or by total laryngectomy with or without adjuvant postoperative irradiation. The obvious advantage of the former strategy, which we use at the University of Florida, is that there is a fairly good chance that the larynx will be preserved.

Although some patients may be rehabilitated with a tracheoesophageal puncture after laryngectomy, only about 20% of patients use this device long term and the majority use an electric larynx (62).

The advanced group is treated with total laryngectomy and neck dissection with or without adjuvant radiation therapy or by radiation therapy and adjuvant chemotherapy (68).

Data suggest that if patients whose tumors show a partial or complete response to two to three cycles of neoadjuvant chemotherapy are then given high-dose radiation therapy, the cure rates are comparable with those obtained with initial total laryngectomy (16).

Another less expensive and less toxic method to select patients likely to be cured by radiation therapy alone is to calculate the primary tumor volume on

pretreatment CT or MRI. Data indicate that primary tumor volume is inversely related to the probability of local control after irradiation (61,64).

Recent data indicate that whereas induction chemotherapy probably does not improve the likelihood of locoregional control and survival, concomitant chemotherapy and irradiation results in an improved possibility of cure compared with irradiation alone (23,68,90).

There is a subset of patients with high volume, unfavorable, advanced cancers who may be cured by chemoradiation but have a useless larynx and permanent tracheostomy and/or gastrostomy (61).

These patients are best treated with a total laryngectomy, neck dissection, and postoperative irradiation.

Carcinoma in Situ

Lesions diagnosed as carcinoma in situ may sometimes be controlled by stripping the cord. However, it is difficult to exclude the possibility of microinvasion on these specimens. Recurrence is frequent, and the cord may become thickened and the voice hoarse with repeated stripping. Localized carcinoma in situ can also be excised using the CO2 laser.

Early radiation therapy for carcinoma in situ often means a better chance of preserving a good voice, especially as many patients with this diagnosis eventually receive this treatment (28).

Many patients with a diagnosis of carcinoma in situ have obvious lesions that probably contain invasive carcinoma. We have often proceeded with radiation therapy rather than put the patient through a repeated biopsy procedure.

Early Vocal Cord Carcinoma

In most centers, irradiation is the initial treatment prescribed for T1 and T2 lesions, with surgery reserved for salvage after radiation therapy failure (60,71).

Although hemilaryngectomy or cordectomy produces comparable cure rates for selected T1 and T2 vocal cord lesions, irradiation is generally preferred (71,79).

Supracricoid laryngectomy, as reported by Laccourreye et al. (47) is a procedure designed to remove moderate-sized cancers involving the supraglottic and glottic larynx. The larynx may be removed with preservation of the cricoid and the arytenoid with its neurovascular innervation, the defect is closed by approximating the base of the tongue to the remaining larynx. The oncologic and functional results of this procedure in selected patients are reported to be excellent.

Transoral laser excision also may provide high cure rates for select patients with small, well-defined lesions limited to the midthird of one true cord (58,103).

A small subset of transoral laser surgeons, notably Professor Steiner, use this technique successfully in moderately advanced cancers (71).

The major advantage of irradiation compared with partial laryngectomy is better quality of the voice. Partial laryngectomy finds its major use as salvage surgery in suitable cases after irradiation failure. Even if the patient has a local recurrence after salvage partial laryngectomy, there is a third chance with total laryngectomy, which may still be successful.

Verrucous lesions have the reputation of being unresponsive to radiation therapy and, in some instances, converting into invasive, often anaplastic, metastasizing lesions. Partial laryngectomy is recommended for early verrucous carcinoma of the glottis, but irradiation is recommended if the alternative is total laryngectomy. We have observed typical verrucous lesions that have disappeared with radiation therapy and not recurred.

O'Sullivan et al. (80) also have made this observation. Additionally, a variety of tumors that recur after unsuccessful treatment (with surgery, radiation therapy, and/or chemotherapy) are more likely to exhibit more aggressive behavior.

Moderately Advanced Vocal Cord Cancer

Fixed-cord lesions (T3) may be subdivided into relatively favorable or unfavorable lesions. Patients with unfavorable lesions usually have extensive bilateral disease with a compromised airway and are considered to be in the advanced group. Patients with favorable T3 lesions have disease confined mostly to one side of the larynx, have a good airway, and are reliable for follow-up. Some degree of supraglottic and subglottic extension usually exists. The extent of disease and tumor volume, in particular, are related to the likelihood of control after radiation therapy (61).

The patient with a favorable lesion is advised of the alternatives of irradiation with surgical salvage or immediate total laryngectomy. Recent data suggest that the likelihood of locoregional control is better after some altered fractionation schedules compared with conventional once-daily radiation therapy (24,68).

Follow-up examinations are recommended every 4 to 6 weeks for the first year, every 6 to 8 weeks for the second year, every 3 months for the third year, every 6 months for the fourth and fifth years, and annually thereafter. The patient must understand that total laryngectomy may be recommended purely on clinical grounds without biopsy-proven recurrence and that the risk of laryngeal osteochondronecrosis is about 5%.

Evaluation of cord mobility after 50.4 Gy or at the end of radiation therapy has not been helpful in predicting local control (64).

Some patients in whom the vocal cord remained fixed have had local tumor control of the disease for 2 years or longer after radiation therapy.

The major difficulty in using irradiation for the more advanced lesions is distinguishing radiation edema from local recurrence during follow-up examinations (87).

Progressive laryngeal edema, persistent throat pain, or fixation of a previously mobile vocal cord frequently signifies recurrent disease in the larynx, although a few patients with these findings remain disease-free with long-term follow-up.

Extended hemilaryngectomy has been used by a few surgeons in the treatment of well-lateralized fixed-cord lesions. A permanent tracheostomy is usually required because a portion of the cricoid is resected, but a useful voice may be retained (88).

Advanced Vocal Cord Carcinoma

Advanced lesions usually show extensive subglottic and supraglottic extension, bilateral glottic involvement, and invasion of the thyroid, cricoid, or arytenoid cartilage, or frequently all three (5,6).

The airway is compromised, necessitating a tracheostomy at the time of direct laryngoscopy in approximately 30% of patients. Clinically positive lymph nodes are found in about 25% to 30% of patients.

The mainstay of treatment is total laryngectomy, with or without adjuvant radiation therapy. The most frequent sites of local failure after total laryngectomy are around the tracheal stoma, in the base of tongue, and in the neck lymph nodes or soft tissues of the neck. If the neck has clinically negative findings before surgery and if postoperative irradiation is planned, neck dissection may be withheld, and radiation therapy may be used to treat both sides of the neck. However, in practice, most surgeons prefer to perform elective bilateral selective (levels II-IV) neck dissections in conjunction with a total laryngectomy for T3N0 or T4N0 laryngeal cancer, even if postoperative irradiation is planned. If the lymph nodes are clinically positive, a therapeutic neck dissection is performed at the time of laryngectomy.

The indications for postoperative radiation therapy include close or positive margins, significant subglottic extension (1 cm or more), cartilage invasion, perineural invasion,

endothelial-lined space invasion, extension of the primary tumor into the soft tissues of the neck, multiple positive neck nodes, extracapsular extension, and control of subclinical disease in the opposite neck (2,41).

Preoperative irradiation is indicated for patients who have fixed neck nodes, have had an emergency tracheotomy through tumor, or have direct extension of tumor involving the skin.

Definitive irradiation is prescribed for the patient who refuses total laryngectomy or is medically unsuitable for major surgery.

As previously stated, there is evidence that two to three cycles of neoadjuvant chemotherapy followed by radiation therapy in patients obtaining at least a partial response may provide a moderate likelihood of larynx preservation without compromising cure (16).

Recent data suggest that concomitant chemotherapy and irradiation is more efficacious than irradiation alone or induction chemotherapy followed by radiation therapy (23,90).

The optimal combination of concomitant chemotherapy and irradiation is unclear (68).

A randomized intergroup trial (Radiation Therapy Oncology Group 91–11) compared three treatment arms: Arm A, three cycles of induction cisplatin and fluorouracil followed by irradiation in complete and partial responders; Arm B, radiation therapy and concomitant cisplatin (100 mg/m2 on days 1, 22, and 43 of radiation therapy); and Arm C, once-daily irradiation (70 Gy in 35 fractions during 7 weeks) alone (23).

Five hundred forty-seven patients were randomized and followed for a median of 3.8 years; 518 patients were evaluable. The rates of larynx preservation were: Arm A, 72%; Arm B, 84%; and Arm C, 67%. The rates of larynx presentation were significantly improved for Arm B; there was no significant difference between Arm A and Arm C. The 5-year survival rates were similar for the three treatment groups: Arm A, 55%; Arm B, 54%; and Arm C, 56%. The likelihood of developing distant metastases was lower for the two groups of patients that received adjuvant chemotherapy.

Surgical Treatment

Cordectomy is an excision of the vocal cord and may be performed by the transoral approach usually with a laser or externally by a thyrotomy. Its use is usually confined to small lesions of the middle third of the cord. After cordectomy, a pseudocord is formed, and the patient has a useful, if somewhat harsh, voice.

Vertical partial laryngectomy (i.e., hemilaryngectomy) allows removal of limited cord lesions with preservation of voice. One entire cord with as much as a third of the opposite cord with the adjacent thyroid cartilage is the maximum cordal involvement suitable for surgery in men; women have a smaller larynx, and usually only one vocal cord may be removed without compromising the airway. Partial fixation of one cord is not a contraindication to hemilaryngectomy, but only a few surgeons have attempted hemilaryngectomy for selected fixed-cord lesions. The maximum subglottic extension suitable for hemilaryngectomy is 8 to 9 mm anteriorly and 5 mm posteriorly; this limit is necessary to preserve the integrity of the cricoid. Tumor extension to the epiglottis, false cord, or both arytenoids is a contraindication to hemilaryngectomy.

Supracricoid partial laryngectomy is used for selected T2 and T3 glottic carcinomas and entails removal of both true and false cords as well as the entire thyroid cartilage. The cricoid is sutured to the epiglottis and hyoid (cricohyoidopexy).

Total laryngectomy with or without neck dissection is the operation of choice for advanced lesions and as a salvage procedure for radiation therapy failures in lesions that are not suited for conservation surgery. The entire larynx is removed, and the pharynx is reconstructed. A permanent tracheostomy is required. Speech may be reconstituted with a prosthesis or with an electrolarynx. One hundred four (63%) of 166 patients entered into the surgery and postoperative irradiation arm of the Veterans Affairs Laryngeal Cancer Study Group randomized trial were evaluable for communication status at 2 years after treatment (38).

Ninety-six patients had undergone a total laryngectomy and communicated as follows: Tracheoesophageal, 27 (28%); esophageal, 5 (5%); artificial larynx, 47 (50%); nonvocal, 7 (7%); and no data, 10 (10%) (38).

One hundred seventy-three patients underwent total laryngectomy and postoperative radiotherapy at the University of Florida and 69 patients were evaluable for 5 years or longer (62). Voice rehabilitation was accomplished as follows: Tracheoesophageal, 19%; artificial larynx, 57%; esophageal, 3%; nonvocal, 14%; and no data, 7%.

Radiation Therapy Technique

Irradiation for T1 or T2 vocal cord cancer is delivered by small portals covering only the primary lesion. The cervical lymph node chain is not electively treated. For T1 lesions, radiation therapy portals extend from the thyroid notch superiorly to the inferior border of the cricoid and fall off anteriorly. The posterior border depends on the posterior extension of the tumor (73). For T2 tumors, the field is extended depending on the anatomic distribution of the tumor. The field size ranges from 4 × 4 cm to 5 × 5 cm (plus an additional 1 cm of “flash” anteriorly) and is occasionally 6 × 6 cm for a large T2 lesion. Portals larger than this increase the risk of edema without improving the cure rate.

A commonly used dose-fractionation schedule at many institutions is 66 Gy for T1 lesions and 70 Gy for T2 cancers given in 2-Gy fractions. Evidence suggests that increasing the dose per fraction may improve the likelihood of local control (4,19,36,37,45,69,97,119). Ample data suggest that 1.8 Gy once daily results in significantly lower local control rates compared with 2 Gy once daily (45). Yamakazi et al. (121) recently reported a prospective trial in which patients with T1N0 squamous cell carcinoma of the glottic larynx were randomized to definitive radiotherapy at 2 Gy per fraction or 2.25 Gy per fraction. The 5-year local control rates were 77% after 2 Gy per fraction and 92% after 2.25 Gy per fraction (p = .004); there was no difference in either acute or late toxicity. Patients with T1 or T2 vocal cord cancer who are treated with once-a-day fractionation at the University of Florida are irradiated with 2.25 Gy per fraction; the dose-fractionation schemes used are shown as follows: Tis–T2 A, 63 Gy in 28 fractions; and T2B, 65.25 Gy in 29 fractions.

At the University of Florida, patients are treated in the supine position; the field borders for a patient with a T1N0 cancer are depicted in Fig. 44.7 (73). The field is checked by the physician at the treatment machine according to palpable anatomic landmarks. This allows the treatment volume to be kept at a minimum and reduces the risk of geographic miss. A three-field technique, using 4-or 6-MV x-rays, is used to deliver approximately 95% of the dose through opposed lateral wedged fields weighted to the side of the lesion; the remaining dose is delivered by an anterior field shifted 0.5 cm toward the side of the lesion (Fig. 44.8) (73). The tumor dose is usually specified at the 95% normalized isodose line.

Irradiation of T3 and T4 lesions requires larger portals, which include the jugulodigastric and middle jugular lymph nodes (Fig. 44.9) (74,85). The inferior jugular lymph nodes are included in a separate low-neck portal. Patients treated at the University of Florida are irradiated in a continuous-course twice daily at 1.2 Gy per fraction to a total dose of 74.4 Gy. The portals are reduced after 45.6 Gy in 38 fractions; the reduced portals cover only the primary lesion.

Intensity-modulated radiation therapy (IMRT) is employed if there is a clear advantage associated with this technique. Disadvantages associated with IMRT include increased dose inhomogeneity, increased total body dose, and increased labor and expense. The most common indications for IMRT for laryngeal cancers are the occasional patients with a node-positive T3–T4 cancer in which the retropharyngeal nodes are electively irradiated and the dose to the contralateral parotid gland reduced and/or a difficult low match between the lateral fields used to treat the primary site and upper neck and the anterior low neck field in a patient with a short neck and large shoulders. In the latter instance, IMRT could be used to encompass the entire target volume and avoid the problem of field junctioning entirely. IMRT is especially useful for patients with extensive subglottic invasion where achieving an adequate inferior margin with conventional lateral portals may not be possible.

Evidence from both retrospective and randomized trials points to improved therapeutic ratios with altered fractionation schedules (68). Given that irradiation is effective treatment for head and neck primary squamous cell carcinoma, it should not be surprising that higher doses of irradiation given more intensively would be more effective at providing tumor control. Because most observers have noted no increase in late toxicity with the various regimens, it generally is concluded that these schedules yield an improved therapeutic ratio. A recently updated Radiation Therapy Oncology Group 90–03 trial (24,109) reported on 1,073 patients who were randomly selected to receive one of four fractionation schedules:

Standard fractionation: 2 Gy per fraction, once a day, 5 days a week, to a total dose of 70 Gy in 35 fractions during 7 weeks;

Hyperfractionation: 1.2 Gy per fraction, twice daily (≥6 hours apart), 5 days a week, to a total dose of 81.6 Gy in 68 fractions during 7 weeks;

Accelerated fractionation with split: 1.6 Gy per fraction, twice daily (≥6 hours apart), 5 days a week, to a total dose of 67.2 Gy in 42 fractions during 6 weeks, including a 2-week rest after 38.4 Gy, or;

Accelerated fractionation with concomitant boost: 1.8 Gy per fraction, once a day, 5 days a week to a large field, plus 1.5 Gy per fraction once a day to a boost field given 6 or more hours after treatment of the large field for the last 12 treatments days, to a total dose of 72 Gy in 42 fractions during 6 weeks.

The 5-year locoregional failure rates were standard fractionation, 59%; hyperfractionation, 51%; accelerated split course, 58%; and concomitant boost, 52%. Both the hyperfractionation and concomitant boost schedules yielded locoregional control rates that were significantly better than standard fractionation. There was a trend toward improved overall survival with hyperfractionation, but no difference in cause-specific survival. Acute toxicity was increased with all three altered fractionation schedules; there was a modest increase in late effects with the concomitant boost schedule.

The treatment technique used for postoperative irradiation after total laryngectomy is depicted in Figure 44.10 (2). The treatment technique for preoperative irradiation is essentially the same as that used for irradiation alone. Alternatively, IMRT may be employed for the indications discussed previously.

Treatment of Recurrence

Most recurrences appear within 18 months, but late recurrences may appear after 5 years. The latter are likely second primary malignancies. The risk of metastatic disease in lymph nodes increases with local recurrence (63).

Recurrence after Radiation Therapy

With careful follow-up, recurrence is sometimes detected before the patient notices a return of hoarseness. There is often minimal lymphedema for 1 to 2 months after irradiation, which usually subsides or stabilizes. An increase in edema, particularly if associated with hoarseness or pain, suggests recurrence, even if there is no obvious tumor. Fixation of a previously mobile

vocal cord usually implies local recurrence, but we have occasionally observed a patient who has experienced a fixed cord with an otherwise normal-appearing larynx and who has not shown evidence of recurrence.

It may be difficult to diagnose recurrence if the tumor is submucosal. Generous, deep biopsies are required. If recurrence is strongly suspected, laryngectomy may rarely be advised without biopsy-confirmed evidence of recurrence. Positron emission tomography may be useful to distinguish recurrent tumor from necrosis.

Radiation therapy failures may be salvaged by cordectomy, hemilaryngectomy, supracricoid partial laryngectomy, or total laryngectomy. Biller et al. (8) reported a 78% salvage rate by hemilaryngectomy for 18 selected patients in whom irradiation failed; total laryngectomy was eventually required in 2 patients. Only two patients died of cancer. These investigators offered guidelines for using hemilaryngectomy: Contralateral vocal cord is normal, arytenoid is not involved, subglottic extension does not exceed 5 mm, and vocal cord is not fixed. In our experience, 14 patients irradiated for T1 or T2 vocal cord cancers underwent a hemilaryngectomy after local recurrence and 8 were successfully salvaged (60).

Recurrence after Surgery

The rate of salvage by irradiation for recurrences or new tumors that appear after initial treatment by hemilaryngectomy is about 50%. Lee et al. (53) reported seven successes among 12 patients; one lesion was later controlled by total laryngectomy. Total laryngectomy can be used successfully to treat hemilaryngectomy failures not suitable for radiation therapy. Irradiation rarely cures patients with recurrence in the neck or stoma after total laryngectomy.

Treatment Selection and Technique: Supraglottic Larynx Carcinoma

Selection of Treatment Modality

Patients with supraglottic laryngeal carcinoma may be considered to be in an early or favorable group suitable for radiation therapy or conservation laryngectomy or an unfavorable group often requiring total laryngectomy.

Early and Moderately Advanced Supraglottic Lesions

Treatment of the primary lesion for the early group is by external-beam irradiation or supraglottic laryngectomy, with or without adjuvant irradiation (39). Transoral laser excision is effective in experienced hands for small, selected lesions (103). Total laryngectomy is rarely indicated as the initial treatment for this group of patients and is reserved for treatment failures.

Radiation therapy and supraglottic laryngectomy are highly successful modes of therapy for early lesions (39). Approximately 50% of supraglottic laryngectomies performed at the University of Florida have been followed by postoperative irradiation because of neck disease and, less often, positive margins.

The decision to use radiation therapy or supraglottic laryngectomy depends on several factors including the anatomic extent of the tumor, medical condition of the patient, philosophy of the attending physician(s), and the inclination of the patient and family. Overall, about 80% of patients are treated initially by irradiation. Approximately half of the patients seen in our clinic whose lesions are technically suitable for a supraglottic laryngectomy are not suitable for medical reasons (e.g., inadequate pulmonary status or other major medical problems); these patients are treated with radiation therapy.

Analysis of local control by anatomic site within the supraglottic larynx shows no obvious differences in local control by irradiation for similarly staged lesions. Invasion of the pre-epiglottic space is not a contraindication to supraglottic laryngectomy or irradiation. Primary tumor volume based on pretreatment CT is inversely related to local tumor control after radiation therapy (61). A large, bulky infiltrative lesion, especially one with extensive preepiglottic space invasion, is a common reason to select supraglottic laryngectomy.

The status of the neck often determines the selection of treatment of the primary lesion. Patients with clinically negative neck nodes have a high risk for occult neck disease and may be treated by radiation therapy or supraglottic laryngectomy and bilateral selective neck dissections, (levels II–IV).

If a patient has an early-stage primary lesion but advanced neck disease (N2b or N3), combined treatment is frequently necessary to control the neck disease (70). In these cases, the primary lesion is usually treated by irradiation alone, with surgery added to the treatment of the involved neck site(s). If the same patient were treated with supraglottic laryngectomy, neck dissection, and postoperative irradiation, the portals would unnecessarily cover the primary site and the neck. If the patient has early, resectable neck disease (N1 or N2a) and surgery is elected for the primary site, postoperative irradiation is added only because of unexpected findings (e.g., positive margins, multiple positive nodes, or extracapsular extension). We prefer to avoid routine high-dose preoperative or postoperative irradiation in conjunction with a supraglottic laryngectomy because the lymphedema of the remaining larynx may be considerable, although it eventually subsides. However, Lee et al. (54) from M.D. Anderson Cancer Center reported excellent results with combined supraglottic laryngectomy and postoperative irradiation for moderately advanced lesions.

Advanced Supraglottic Lesions

Although a subset of these patients may be suitable for a supraglottic or supracricoid laryngectomy, total laryngectomy is the main surgical option. Selected advanced lesions, especially those that are mainly exophytic, may be treated by radiation therapy and concomitant chemotherapy (90) with total laryngectomy reserved for irradiation failures.

For patients whose primary lesion is to be treated by a total or partial laryngectomy and who have resectable neck disease, surgery is the initial treatment, and postoperative irradiation is added if needed. If the neck disease is unresectable, preoperative radiation therapy is used. The indications for preoperative and postoperative irradiation have been previously outlined.

Surgical Treatment

Supraglottic Laryngectomy

Supraglottic laryngectomy is voice-sparing surgery that can be used successfully for selected lesions involving the epiglottis, a single arytenoid, the aryepiglottic fold, or the false vocal cord. Extension of the tumor to the true vocal cord, the anterior commissure, or both arytenoids; fixation of the vocal cord; or thyroid or cricoid cartilage invasion precludes supraglottic laryngectomy. The supraglottic laryngectomy may be extended to include the base of the tongue if one lingual artery is preserved.

All patients have difficulty swallowing with a tendency to aspirate immediately after surgery, but almost all learn to swallow again in a short time; motivation and the amount of tissue removed are key factors in learning to swallow again. Preoperatively, adequate pulmonary reserve is evaluated by blood gas determinations, function tests, chest roentgenography, and a work test involving walking the patient up two flights of stairs to determine tolerance to pulmonary stress. The voice quality is generally normal after supraglottic laryngectomy.

Supracricoid Laryngectomy

This procedure is an option for lesions extending from the supraglottis into one or both vocal cords. However, vocal cord fixation is a relative contraindication. At least one arytenoid must be preserved for successful decannulation and phonation. Extension to the cricoid and thyroid cartilage destruction also preclude its use. Phonation and respiratory function are reconstituted by approximating the cricoid to the hyoid (cricohyoidopexy).

Wide-Field Total Laryngectomy

Total laryngectomy is performed as previously described.

Radiation Therapy Technique

The primary lesion and both sides of the neck are treated with opposed lateral portals; wedges are used to compensate for the contour of the neck (Fig. 44.11) (73). The lower neck nodes are irradiated through a separate anterior portal. IMRT may be employed to spare one or both parotids and to avoid a low match line in the occasional patient with a short neck and large shoulders. We currently use the concomitant boost fractionation schedule when employing IMRT.

In the case of clinically positive nodes, an electron beam portal may be used to increase the dose to the posterior cervical nodes after the fields are reduced to avoid the spinal cord at 45 Gy. CT is obtained 4 weeks after completing radiotherapy, and a neck dissection is added if the residual cancer in the nodes is thought to exceed 5%; otherwise the patient is observed and a CT is repeated in 3 months (70).

Patients experience a sore throat, loss of taste, and moderate dryness during irradiation. Edema of the arytenoids may occur and give a sensation of a lump in the throat. Tracheostomy is rarely necessary, even for bulky lesions.

Edema of the larynx may persist for several months to a year. Patients who continue to smoke heighten the side effects of dryness, dysphagia, and hoarseness.

Preoperative and Postoperative Treatment Technique

If total laryngectomy is required and the lesion is resectable, postoperative radiation therapy is preferred because there is no evidence that preoperative irradiation produces any better locoregional control or survival rates than surgery and postoperative radiation therapy. Irradiation is added for close or positive margins, invasion of soft tissues of the neck, significant subglottic extension (1 cm or more), thyroid cartilage invasion, multiple positive nodes, and extracapsular extension. The high-risk areas are usually the base of the tongue and the neck.

The dose for postoperative irradiation as a function of known residual disease is as follows: Negative margins, 60 Gy in 30 fractions; microscopically positive margins, 66 Gy in 33 fractions; and gross residual disease, 70 Gy in 35 fractions. All patients are treated with a continuous course, one fraction per day, 5 days per week. The lower neck is treated with doses to 50 Gy in 25 fractions at Dmax. If there is subglottic extension, the dose to the stoma is boosted with electrons (usually 10 to 14 MeV) for an additional 10 Gy in five fractions. The treatment technique is shown in Fig. 44.10 (2). If postoperative irradiation is added after a supraglottic laryngectomy, the dose is lowered to 55.8 Gy

given in 1.8 Gy fractions. This dose produces acceptable rates of local control and laryngeal edema (94).

The treatment technique used for preoperative radiation therapy is essentially the same as that used for patients treated with irradiation alone, using doses of 50 to 60 Gy at 1.8 to 2 Gy per fraction. Thereafter, the dose is boosted to areas of unresectable disease (usually the neck) to total doses ranging from 65 to 70 Gy.

Treatment of Recurrence

Failures after supraglottic laryngectomy or radiation therapy can frequently be controlled by further treatment; therefore, recognition of recurrence should be vigorously pursued (39). Salvage of patients with recurrence after combined total laryngectomy and irradiation is uncommon. Stomal recurrences are occasionally controlled by radiation therapy or surgery.

Results of Treatment

Vocal Cord Cancer

The local control and survival rates after treatment of early-stage glottic carcinoma are depicted in Tables 44.3, 44.4, 44.5 and 44.6 (71). The local control and survival rates are similar for transoral laser excision, open partial laryngectomy, and radiotherapy. Larynx preservation rates are also comparable. Voice quality depends on the amount of tissue removed with partial laryngectomy and is probably similar for patients with limited lesions treated with laser to those undergoing radiotherapy and poorer for patients undergoing open partial laryngectomy (71).

Foote et al. (22) reported on 81 patients who underwent laryngectomy for T3 cancers at the Mayo Clinic between 1970 and 1981. Seventy-five patients underwent a total laryngectomy and 6 underwent a near-total laryngectomy; 53 patients received a neck dissection. No patient underwent adjuvant irradiation or chemotherapy. The 5-year rates of locoregional control, cause-specific survival, and absolute survival were 74%, 74%, and 54%, respectively. The results of definitive radiation therapy patients with T3 glottic carcinoma are depicted in Table 44.7 (85) and are similar to the surgical outcomes reported by Foote et al. (22).

The survival and control rates of patients with T3 fixed-cord lesions treated at the University of Florida are presented in Table 44.8 (67). There was no relationship between subsequent local control and whether the vocal cord remained fixed or became mobile during irradiation. The incidence of severe complications, including those after the initial treatment and any later salvage procedures, was 15% after radiation therapy alone and 15% after surgery alone or combined with adjuvant irradiation. The vocal quality varied from fair to nearly normal.

The results of treatment of T4 vocal cord carcinoma in four surgical series and two radiotherapy series are summarized in Table 44.9 (35).

Parsons et al. (86) reviewed the literature and reported a local control rate of 62% in a series of 87 patients treated with irradiation alone for T4 glottic carcinoma.

Combined-Therapy Results

The proportion of patients suitable for a supraglottic laryngectomy is depicted in Table 44.10 (39). Depending on the referral patterns, a modest subset of patients is suitable for this operation. The extent of neck disease for patients treated with either surgery or radiotherapy is shown in Table 44.11 (39). In general, patients treated with supraglottic laryngectomy appropriately have earlier stage neck disease and would be anticipated to have a lower risk of distant failure and improved survival. The local control rates after transoral laser, radiotherapy, and supraglottic laryngectomy are summarized in Tables 44.12, 44.13 and 44.14, respectively (39). In general, the local control rates after transoral laser excision are fairly good for patients with T1–T2 tumors and tend to deteriorate for those with more advanced disease. The local control rate are excellent for patients selected for supraglottic laryngectomy. However, the incidence of severe complications tends to be higher after supraglottic laryngectomy compared with radiotherapy and transoral laser excision (Table 44.15) (39).

Follow-Up Policy

Follow-up of patients with early lesions is planned for every 4 to 8 weeks for 2 years, every 3 months for the third year, and every 6 months for years 4 and 5, and then annually for life.

Follow-up of patients with vocal cord or supraglottic larynx lesions treated by radiation therapy or conservative surgery is almost more important than the treatment itself because early detection of recurrence usually results in salvage that may include cure with voice preservation.

If recurrence is suspected but the biopsy is negative, patients are reexamined at 2- to 4-week intervals until the matter is settled. The value of follow-up CT scans for detecting early local recurrence is investigational.

Wagenfeld et al. (112) studied 740 cases of glottic larynx cancer treated from 1965 to 1974 to determine the incidence of second respiratory tract malignancies. There was a minimum follow-up of 5 years. There were 48 second respiratory tract malignancies, although only 14 were expected. Twenty-five were in the lung, and 23 were scattered among other head and neck sites. Only 7 of the 23 second head and neck primary lesions resulted in death; these second lesions were frequently diagnosed in an early stage during routine follow-up for the glottic lesion.

Because the risk of a lethal lung primary lesion is nearly as great as that of dying of an early glottic carcinoma, it makes sense to obtain annual chest roentgenograms. Approximately 50% of patients who receive moderate-to-high dose radiotherapy to the entire thyroid gland will develop hypothyroidism within 5 years, so that thyroid functions are checked every 6 to 12 months and thyroid replacement is initiated if the thyroid-stimulating hormone level begins to rise (27).

Sequelae of Treatment

Surgical Sequelae

Neel et al. (78) reported a 26% incidence of nonfatal complications for cordectomy. Immediate postoperative complications included atelectasis and pneumonia, severe subcutaneous emphysema in the neck, bleeding from the tracheotomy site or larynx, wound complications, and airway obstruction requiring tracheotomy. Late complications included granulation tissue that had to be removed by direct laryngoscopy to exclude recurrences, extrusion of cartilage, laryngeal stenosis, and obstructing laryngeal web.

The postoperative complications and sequelae of hemilaryngectomy include chondritis, wound slough, inadequate glottic closure, and anterior commissure webs (25). The complications associated with supraglottic laryngectomy and total laryngectomy for supraglottic carcinomas include fistula (8%), carotid artery exposure or blowout (3% to 5%), infection or wound sloughing (3% to 7%), and fatal complications (3%) (25). The risk of complications increased if tumor margins were involved by tumor; there was no change in risk associated with age, sex, race, laryngeal site, stage of primary tumor, size of primary tumor, use of low-dose preoperative irradiation, or status of the positive nodes.

The incidence of complications after treatment of supraglottic carcinoma is depicted in Table 44.15 (39).

Radiation Therapy Sequelae

The acute reactions from the treatment of early vocal cord cancer using a tumor dose of 2.25 Gy per day to administer a total dose 63 Gy (60Co, five fractions per week) are relatively mild. During the first 2 to 3 weeks, the voice may improve as the tumor regresses. The voice generally becomes hoarse again because of radiation-induced changes, even though the tumor continues to regress. A mild sore throat develops beginning at the end of the second week, but medication is usually not required. The voice begins to improve approximately 3 weeks after completion of treatment, usually reaching a plateau in 2 to 3 months. Patients with extensive lesions often recover a normal voice, although not as frequently as those with small tumors.

Edema of the larynx is the most common sequela after irradiation for glottic or supraglottic lesions. The rate of clearance of the edema is related to the irradiation dose, volume of tissue irradiated, addition of a neck dissection, continued use of alcohol and tobacco, and size and extent of the original lesion. Edema may be accentuated by a radical neck dissection and may require 6 to 12 months to subside.

Soft tissue necrosis leading to chondritis occurs in fewer than 1% of patients, usually in those who continue to smoke. Soft tissue and cartilage necroses mimic recurrence, with hoarseness, pain, and edema; a laryngectomy may be recommended as a last resort for fear of recurrent cancer, even though biopsy specimens show only necrosis.

Corticosteroids such as dexamethasone (Decadron) have been used to reduce radiation-induced edema after recurrence has been ruled out by biopsy. If ulceration and pain occur, administration of an antibiotic such as tetracycline may help. Of 519 patients with T1N0 or T2N0 vocal cord cancer treated at the University of Florida, 5 (1%) experienced severe complications (60), including total laryngectomy for a suspected local recurrence (1 patient), permanent tracheostomy for edema (3 patients), and a pharyngocutaneous fistula after a salvage total laryngectomy (1 patient).

In patients irradiated for supraglottic carcinoma, sore throat persists 3 to 4 weeks after completion of treatment. There is an associated dry mouth from irradiation of the salivary and parotid glands, a loss of taste, and a sensation of a lump in the throat. It is unusual for patients to require a tracheotomy before irradiation unless severe lymphedema develops at the time of direct laryngoscopy and biopsy. However, in patients who have recovered from the direct laryngoscopy and biopsy without obstruction, a tracheotomy has rarely been required during a fractionated course of radiation therapy.

Patients treated twice a day with 1.2 Gy fractions (continuous-course technique) to total doses of 74.4 to 76.8 Gy usually have more brisk acute reactions than those treated once a day with 2-Gy fractions. Approximately 20% treated with twice-a-day irradiation require temporary gastrostomy feeding tubes because they have difficulty in swallowing (1).

Examples of acute chondritis requiring discontinuation of treatment have not been seen, although most epiglottic lesions exhibit cartilage invasion.

The epiglottis, both suprahyoid and infrahyoid portions, remains thicker than normal for long periods of time, but this is not often associated with difficulty in swallowing, respiratory obstruction, or aspiration. The patient is cautioned to eat and drink slowly until the edema resolves. The false cord and arytenoids may develop some edema.

Lesions of the suprahyoid epiglottis frequently destroy the tip of the epiglottis, and it may require some time for the exposed cartilage to heal. Successful irradiation of infrahyoid epiglottis tumors is not associated with a high rate of necrosis, even though most of these lesions penetrate the porous epiglottic cartilage.

The incidence of severe late complications in 274 patients treated with radiation therapy alone or combined with neck dissection at the University of Florida was 4% (39).

Radiation Therapy Sequelae

The acute reactions from the treatment of early vocal cord cancer using a tumor dose of 2.25 Gy per day to administer a total dose 63 Gy (60Co, five fractions per week) are relatively mild. During the first 2 to 3 weeks, the voice may improve as the tumor regresses. The voice generally becomes hoarse again because of radiation-induced changes, even though the tumor continues to regress. A mild sore throat develops beginning at the end of the second week, but medication is usually not required. The voice begins to improve approximately 3 weeks after completion of treatment, usually reaching a plateau in 2 to 3 months. Patients with extensive lesions often recover a normal voice, although not as frequently as those with small tumors.

Edema of the larynx is the most common sequela after irradiation for glottic or supraglottic lesions. The rate of clearance of the edema is related to the irradiation dose, volume of tissue irradiated, addition of a neck dissection, continued use of alcohol and tobacco, and size and extent of the original lesion. Edema may be accentuated by a radical neck dissection and may require 6 to 12 months to subside.

Soft tissue necrosis leading to chondritis occurs in fewer than 1% of patients, usually in those who continue to smoke. Soft tissue and cartilage necroses mimic recurrence, with hoarseness, pain, and edema; a laryngectomy may be recommended as a last resort for fear of recurrent cancer, even though biopsy specimens show only necrosis.

Corticosteroids such as dexamethasone (Decadron) have been used to reduce radiation-induced edema after recurrence has been ruled out by biopsy. If ulceration and pain occur, administration of an antibiotic such as tetracycline may help. Of 519 patients with T1N0 or T2N0 vocal cord cancer treated at the University of Florida, 5 (1%) experienced severe complications (60), including total laryngectomy for a suspected local recurrence (1 patient), permanent tracheostomy for edema (3 patients), and a pharyngocutaneous fistula after a salvage total laryngectomy (1 patient).

In patients irradiated for supraglottic carcinoma, sore throat persists 3 to 4 weeks after completion of treatment. There is an associated dry mouth from irradiation of the salivary and parotid glands, a loss of taste, and a sensation of a lump in the throat. It is unusual for patients to require a tracheotomy before irradiation unless severe lymphedema develops at the time of direct laryngoscopy and biopsy. However, in patients who have recovered from the direct laryngoscopy and biopsy without obstruction, a tracheotomy has rarely been required during a fractionated course of radiation therapy.

Patients treated twice a day with 1.2 Gy fractions (continuous-course technique) to total doses of 74.4 to 76.8 Gy usually have more brisk acute reactions than those treated once a day with 2-Gy fractions. Approximately 20% treated with twice-a-day irradiation require temporary gastrostomy feeding tubes because they have difficulty in swallowing (1).

Examples of acute chondritis requiring discontinuation of treatment have not been seen, although most epiglottic lesions exhibit cartilage invasion.

The epiglottis, both suprahyoid and infrahyoid portions, remains thicker than normal for long periods of time, but this is not often associated with difficulty in swallowing, respiratory obstruction, or aspiration. The patient is cautioned to eat and drink slowly until the edema resolves. The false cord and arytenoids may develop some edema.

Lesions of the suprahyoid epiglottis frequently destroy the tip of the epiglottis, and it may require some time for the exposed cartilage to heal. Successful irradiation of infrahyoid epiglottis tumors is not associated with a high rate of necrosis, even though most of these lesions penetrate the porous epiglottic cartilage.

The incidence of severe late complications in 274 patients treated with radiation therapy alone or combined with neck dissection at the University of Florida was 4% (39).

sabato 14 gennaio 2012

66_00d epidemiology

Epidemiology
The American Cancer Society estimated that in 2007 there were 11,150 new cases of invasive carcinoma of the cervix in the United States and about 3,500 deaths, in addition to over 60,000 cases of carcinoma in situ (279). However, cervical cancer is highly prevalent in developing nations; it is estimated that close to 500,000 women worldwide develop this tumor and 233,000 die of the disease (262). Cervical cancer is more common in Latin America and less frequent in Jewish and European women and Fiji Islanders (250). Although some researchers have attributed the low frequency of cervical carcinoma in Jewish women to the circumcision of Jewish men (602), this low incidence has not been demonstrated in sexual partners of non-Jewish circumcised men. Lynch et al. (390) noted that although Ashkenazi women have an overall cancer risk comparable to other ethnic groups, it is still lower for carcinoma of the cervix, which occurs infrequently in Jewish women.
Carcinoma of the uterine cervix can be induced in experimental animals by application of hormonal or other chemical
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carcinogens (287). However, no definite evidence exists linking the use of oral contraceptives with carcinoma of the uterine cervix (127,188). The association of prenatal exposure to diethylstilbestrol (DES) and development of clear-cell adenocarcinoma of the cervix or vagina in young women has been reported; the overall incidence is thought to be small (0.14 to 1.4 per 1,000 DES-exposed women) (243). Clear cell adenocarcinoma of the cervix unrelated to DES exposure has been described (293).

A large proportion of cervix cancer can be characterized as a sexually transmitted disease, with early age of first intercourse, history of multiple sexual partners, and large number of pregnancies as risk factors (85,309). Epidemiological studies relating genital herpetic infection to cervical cancer have been reported (432). The role of human papilloma virus (HPV) as a causative agent of cervical cancer is well established (50,665), and the detection of HPV types 16 and 18, predominantly, carries prognostic importance in some studies (509,668). Bosch et al. (51) noted that HPV 16 predominated in squamous-cell carcinoma, whereas in adenocarcinoma and adenosquamous carcinoma HPV 18 predominated.
The male partner's role as a potential carrier of HPV is evidenced by the higher incidence of cervical cancer among women whose spouses are known or suspected to have had higher exposure to HPV (6) or whose partner has a history of penile carcinoma (274). Boon et al. (47) characterized the male partner as potential “vector and victim” of HPV, especially in countries where the rate of male circumcision is low.
In June 2006, the U.S. Food and Drug Administration approved the quadrivalent human papillomavirus recombinant vaccine for women 9 to 26 years for prevention of gynecological disease caused by HPV types 6, 11, 16, and 18. This is an exciting development and a landmark decision, heralded as a major advance in the prevention of cervical cancer that may have a worldwide impact on the incidence of this malignancy.
Other risk factors among HIV-positive women included racial/ethnic background (African American vs. white, relative risk [RR] = 1.64), current smoking (yes vs. no, RR = 1.55), and younger age (younger than 30 years vs. 40 years or older, RR = 1.75) (457).
An association between cigarette smoking and development of cervical cancer has been reported (32,187). A review of over 50 studies concluded that smoking was a cofactor for HPV infection and induction of cervical cancer (594). However, in the study by Agarwal et al. (6), cigarette smoking was not a risk factor.
Natural History and Patterns of Spread
Squamous-cell carcinoma of the uterine cervix usually originates at the squamous columnar junction (transformation zone) of the endocervical canal and the portio of the cervix. The lesion is frequently associated with severe cervical dysplasia and carcinoma in situ, usually progressing to invasive carcinoma over 10 to 20 years in the majority of patients (30,84).
The malignant process breaks through the basement membrane of the epithelium and invades the cervical stroma. Formerly, if the invasion was <3 mm, the lesion was classified as microinvasive or superficially invasive (84), a term not used in the International Federation of Gynecologists and Obstetricians (FIGO) staging, which classifies this tumor as Ia1. Invasion may progress, and in a modification of the FIGO staging schema (272), if a tumor is not grossly visible but has a depth of penetration of <5 mm and breadth of 7 mm or less, it is classified as stage IA2 invasive carcinoma; the incidence of metastatic pelvic lymph nodes is related to the depth of invasion, with an overall incidence of 3% to 8% (42,84).
The lesion may eventually be manifested by superficial ulceration, exophytic tumor in the ectocervix, or extensive infiltration of the endocervix. The tumor, if untreated, may spread to the adjacent vaginal fornices or to the paracervical and parametrial tissues (270), with eventual direct invasion of the bladder, the rectum, or both. Landoni et al. (352), in operative specimens of 230 radical hysterectomies with pelvic lymphadenectomy of patients with clinical stage IB and IIA, noted the tumor spreads endocervically equally in all directions; tumor extension into the vesicocervical ligament (anterior para-metrium) was noted in 23% of cases, into the uterosacral ligaments (posterior parametrium) and the rectovaginal septum in approximately 15%, and into the parametria in 28% to 34% of cases. Paracervical extension was related to the depth of stromal invasion, tumor size, lymphatic invasion, and presence of lymph node metastasis.
Carcinoma of the uterine cervix has been found to extend into the lower uterine segment and the endometrial cavity in 10% to 30% of patients (470). Perez et al. (470) and Chao et al. (73) noted decreased survival and a greater incidence of distant metastases in patients with stromal endometrial invasion or replacement of normal endometrium by cervical carcinoma. Regional lymphatic or hematogenous spread occurs, depending on the stage of the tumor, but dissemination does not always follow an orderly sequence, and occasionally a small carcinoma may be seen infiltrating the pelvic lymph nodes, invading the bladder or rectum, or producing distant metastasis.
In addition to the frequently described pelvic lymph nodes, Girardi et al. (178), in 359 specimens of radical hysterectomies, found parametrial nodes in 280 patients (78%); the incidence of positive nodes was 11.4% in stage IB and 21.5% in stage IIB disease. With negative parametrial nodes, only 26% of patients had positive iliac lymph nodes, whereas 81% of patients with positive parametrial lymph nodes also had metastatic pelvic nodes. These data underscore the need to irradiate the parametrial tissues or carry out a complete bilateral pelvic lymphadenectomy in patients with invasive cervical carcinoma.
Carcinoma of the cervix may spread to the obturator lymph nodes (considered a medial group of the external iliac), to other external iliac nodes, and to the hypogastric lymph nodes. From these, there may be tumor metastases to the common iliac or para-aortic lymph nodes (242). The incidence of metastasis to pelvic or para-aortic lymph nodes for various stages of the disease is listed in Tables 66.1 and 66.2.
In 225 patients with carcinoma of the cervix treated with radical hysterectomy and pelvic lymphadenectomy, 13/91 (14.2%) with stage IB and IIA, 16/81 (19.8%) with stage IIB, and 11/40 (28%) with stage IIIB disease had positive pelvic lymph nodes (34). The most commonly involved groups were the parametrial, obturator, external iliac, and common iliac nodes (Fig. 66.3). Para-aortic lymph nodes were involved in
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3/91 (3.3%) patients with stage IB and IIA tumors 4 cm or less and in 5/38 patients (13.1%) with stage IIB and III disease.

Hematogenous dissemination through the venous plexus and the paracervical veins occurs less frequently but is relatively common with more advanced stages. In an analysis of 322 patients in whom distant metastases developed, the most frequently observed metastatic sites were the lung (21%), para-aortic lymph nodes (11%), abdominal cavity (8%), and supraclavicular lymph nodes (7%) (151). Bone metastases occurred in 16% of patients, most commonly to the lumbar and thoracic spine (Table 66.3). Spinal epidural compression from metastatic tumor, often involving lumbar segments, can occur rarely (15), and metastasis to the brain and the heart have been reported (372,394).
Clinical Presentation
Intraepithelial or early invasive carcinoma of the cervix can be detected before it becomes symptomatic by cytologic smears; Papanicolaou (Pap) smear, colposcopy and biopsies, and HPV testing have high specificity and sensitivity (94.5%)
Frequently, the first manifestation of abnormality is postcoital spotting, which may increase to metrorrhagia (intermenstrual bleeding) or more prominent menstrual bleeding (menorrhagia). Serosanguineous or yellowish, foul-smelling vaginal discharge may be noted in patients with advanced invasive carcinoma. If chronic bleeding occurs, the patient may complain of fatigue or other symptoms related to anemia.
Pain in the pelvis or hypogastrium may be caused by tumor necrosis or associated pelvic inflammatory disease. In patients with pain in the lumbosacral area, the possibility of para-aortic lymph node involvement with extension into the lumbosacral roots or hydronephrosis should be considered.
Urinary and rectal symptoms (hematuria, rectal bleeding) may appear in advanced stages as a consequence of invasion of the bladder or rectum by the neoplasm.
Diagnostic Work-Up
Every patient should be jointly evaluated by the radiation and gynecologic oncologists. After careful clinical history a general physical examination with attention to the supraclavicular (nodal) areas, abdomen, and liver, a careful pelvic examination should be carried out with as little discomfort to the patient as possible, without compromising the thoroughness of the evaluation (447). Pelvic examination should include inspection of external genitalia, vagina, and uterine cervix, rectal examination, and bimanual palpation of the pelvis. Pelvic examination under anesthesia is very important in the evaluation and clinical staging of these patients. Cystoscopy or rectosigmoidoscopy should be performed in all patients with stage IIB, III, and IVA disease or those with earlier stages who have a history of urinary or lower gastrointestinal tract disturbances. The diagnostic procedures for carcinoma of the cervix are presented in Table 66.4.
Screening
The American Cancer Society has recommended that asymptomatic women 20 years of age and older or sexually active younger than 20 years have annual Pap smears for 2 consecutive years and at least one every 3 years until the age of 65 years. The American College of Obstetricians and Gynecologists has strongly recommended that that Pap smears be obtained on an annual basis.
When obtaining the Pap smear, special attention should be directed to not using a lubricating agent (warm water on the speculum will suffice), to obtaining good “scrapings” from the cervix and vaginal posterior fornix (without blood), and to using a small brush to obtain an endocervical sample. The patient should be instructed not to cleanse with a douche before the examination, and specimens should be obtained for studies of
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trichomonas. If the cytologic smear shows atypia or mild dysplasia (class II), the smear should be repeated no sooner than after 2 weeks, to allow representative cellular exfoliation.

Guidelines for reporting results of cervical and vaginal cytology were promulgated in 1988. The Bethesda system eliminated the classes of Pap cytology. The correlation between the cytologic diagnosis and subsequent histologic examination is over 90% (334). This system was modified in 1991 and in 2001 (565).
If the cytologic smear shows dysplasia or malignant cells, directed biopsies at colposcopy should be carried out immediately. Endocervical curettage must always be performed except in pregnant women. If the biopsy results are negative, the procedure should be repeated and, if necessary, a conization should be performed.

Conization/Loop Excision
Conization must be performed when no gross lesion of the cervix is noted and an endocervical tumor is suspected; the entire lesion cannot be seen with the colposcope; diagnosis of microinvasive carcinoma is made on biopsy; discrepancies are found between the cytologic and the histologic appearances of the lesion; or the patient is not reliable for continuous follow-up.
Conization involves a conical removal of a large portion of the ectocervix and endocervix. Cold biopsy specimens should always be obtained with a scalpel or other appropriate instrument. At least 50% of the endocervical canal should be removed without compromising the internal sphincter. Curettage of the remaining endocervical canal should be carried out.
Laser conization and loop diathermy excision have achieved some popularity in recent years. Loop excision or laser conization is frequently done in an office setting as an alternative to conization; loop excision is less expensive and more reliable than laser conization (505).
Biopsy
When a gross lesion of the cervix is present, multiple punch biopsies should be adequate to confirm the diagnosis of invasive carcinoma. Specimens should be obtained from any suspect area as well as in all four quadrants of the cervix and from any suspect areas in the vagina. It is important to obtain tissue from the periphery of the lesion with some adjoining normal tissue; biopsy specimens from central ulcerated or necrotic areas may not be adequate for diagnosis.
Dilatation and Curettage
Because possible upper extension of the tumor may modify the plan of therapy, fractional curettage of the endocervical canal and the endometrium is recommended at the time of initial evaluation, or during the first intracavitary radioisotope insertion if the patient is treated with radiation therapy.
Laboratory Studies
For invasive carcinoma, patients should have the following laboratory studies: complete peripheral blood evaluation, including hemogram, white blood cell count, differential and platelet count; blood chemistry profile, with particular attention to blood urea nitrogen, creatinine, and uric acid; liver function values; and urinalysis.
Imaging Studies
Traditionally, chest radiographs and intravenous pyelograms (IVP) were obtained in all patients for staging purposes. The IVP in many countries has been replaced by CT scan of the pelvis and abdomen with contrast material. A colon barium enema should be performed in patients with stage IIB, III, and IVA disease as well as those with earlier stages who have symptoms referable to the colon and rectum.
Pedal lymphangiography was used to assess lymph node involvement in the pelvic or para-aortic nodes. Unfortunately, not all of the lymph nodes to which carcinoma of the cervix may metastasize are opacified (i.e., obturator or hypogastric nodes), small metastatic lesions do not modify the architecture of the lymph node apparent on the lymphangiogram, and at times the metastatic tumor completely obliterates the lymph node or obstructs lymphatics, preventing visualization of the involved lymph nodes (478). Lagasse et al. (346) found the lymphangiogram to be unreliable as a basis for treatment decisions. This procedure has been replaced by CT scanning or MRI.
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If performed with intravenous (IV) contrast, CT scans substitute for IVP. The cervical tumor may be seen as an enlarged, irregular, hypoechoic cervix or as a mass with ill-defined margins. The overall accuracy of CT scanning in staging cervical cancer ranges from 63% to 88% (321). In the detection of lymph node abnormalities, the overall accuracy of conventional CT scanning is 77% to 85%, with a sensitivity of 44% and specificity of 93% (264).
Camilien et al. (67) reported on 61 patients with carcinoma of the cervix who had both preoperative CT scans and exploratory laparotomy; correlation of radiographic and surgical/pathologic findings showed that 75% of the enlarged pelvic lymph nodes on CT contained metastases and 97% of patients with negative nodes on CT scan were pathologically negative (specificity of 97%). However, histologically positive pelvic nodes were often missed on CT scan (sensitivity of 25%). The CT scan is more valuable in evaluation of the para-aortic lymph nodes (specificity of 100% and sensitivity of 67%; Table 66.5).
Shepherd et al. (554), in a retrospective study of CT scans in 56 patients with carcinoma of the cervix treated with irradiation, noted that tumor depth was correlated with lymph node involvement (p <0.01) and risk of death.
Heller et al. (239) reported a prospective evaluation of 320 patients with stage IIB to IVA carcinoma of the cervix entered into a Gynecologic Oncology Group (GOG) protocol in which preoperative CT scan, lymphangiography, and ultrasonography of the aortic area were performed. Para-aortic node dissection was done in patients with negative staging studies. Lymphangiography, CT scan, and ultrasonography had false-negative frequencies for pelvic lymph node evaluation of 14.2%, 25%, and 30%, respectively. The sensitivity was 79% for lymphangiography, 34% for CT scan, and 19% for ultrasonography and the specificity ratings were 73%, 96%, and 99%, respectively. Ultrasonography, therefore, is not reliable in preoperative detection of lymph node metastases, but it has limited value in evaluating extrauterine tumor involvement and may be used to detect uterine perforation, which can occur during intracavitary insertion (661).
MRI is being used more frequently for assessment of extracervical tumor extension (265), although it is somewhat more expensive. MRI is very useful in patients allergic to iodinated contrast material or impaired renal function. It is contraindicated in patients with pacemakers, cochlear implants, metallic prostheses, or large vascular clips. On T2-weighted images, a cervical cancer may be seen as a mass of intermediate signal intensity, usually of greater intensity than the fibrocervical stroma. On T1-weighted images, tumors are usually isointense with the normal cervix and may not be seen (24). Abnormal, irregular cervix margins, prominent parametrial strands, exocentric parametrial enlargement, and loss of parametrial fat planes on T1-weighted images or high signal in the parametria or cardinal/uterosacral ligaments on T2-weighted images are indicative of more extensive tumors (264,321,561). Parametrial tumor is easily identified on T2-weighted images from the low-intensity cervix and uterine ligaments.
Hawnaur et al. (236) compared pretreatment tumor staging and volume assessment by examination under anesthesia (EUA), transrectal ultrasonography (TRUS), and MRI in 60 patients with invasive carcinoma of the cervix. TRUS and MRI assigned the same tumor stage in only 30% of patients, and EUA and MRI agreed on tumor stage in an additional 27%. In cases of disagreement, the MRI staging correlated better with outcome than TRUS or EUA. Sixty-two percent of patients with enlarged lymph nodes on pretreatment MRI either died or had tumor recurrence or metastases. MRI was superior in assessing the full extent of bulky tumors and lymph node enlargement over both TRUS and EUA.
Hatano et al. (235) also evaluated MRI in 42 patients with advanced cervical cancer treated with external irradiation and high–dose-rate (HDR) brachytherapy. In biopsies performed immediately after radiation therapy (RT), no residual tumors were found in 36 patients (86%). The simultaneous MRI study demonstrated no high-signal intensity on T2-weighted images in 28 patients (75%). A high–signal-intensity area was observed in 14 patients, and this disappeared 3 months after RT in eight patients with a negative histologic study. The sensitivity, specificity, and accuracy of MRI tumor response studies at 3 months after radiation therapy were 100%. MRI studies performed at 30 Gy of external irradiation and 3 months after radiation therapy were predictive for local tumor control.
Postema et al. (494) compared MRI with pelvic examination (including under general anesthesia in selected patients) in 103 patients with invasive cervical carcinoma. The gold standard for comparing treatment decisions was based on surgicopathologic data available in 91 patients. MRI was better at identifying extracervical tumor spread, but it had more false-positive results. The pelvic examination led to correct treatment decisions in 89% of patients, with MRI not leading to an overall improvement in treatment decisions.
Also, in a study by Hansen et al. (230), clinical assessment was superior to low-field MRI in staging cervical cancer in 95 women on whom MRI examinations and clinical staging according to the FIGO recommendations were performed within 2 weeks after clinical diagnosis; the clinical staging correctly classified 57 patients (accuracy, 92%), compared with 52 patients with MRI using contrast enhancement (accuracy, 84%).
MRI dynamic enhancement during the first 2 weeks of radiation therapy may provide early prediction of tumor regression rate. In seven patients, tumor regression rates ranged from 2% to 15.2% per day and correlated positively with changes in both peak and mean tumor enhancement (p <0.01). A similar study was published by Gong et al. (181) and van de Bunt et al. (627). MRI also was found to be useful in providing accurate target volume definition in brachytherapy treatment planning (122).
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Haider et al. (218) evaluated 56 patients with adenocarcinoma involving the cervix using MRI and noted that 42 (75%) had a visible mass. Findings were more prevalent in patients with primary adenocarcinoma of the endometrium, as characterized by a endometrial thickening (11 [73%] vs. 3 [13%]) endometrial cavity expansion by a mass (9 [60%] and 2 [9%] respectively) (p = 0.003).
Kodaira et al. (331) reviewed 84 patients with stage II cancer evaluated by MRI; all patients received intracavitary brachytherapy with (83) or without (1) external-beam radiation therapy (EBRT). The 5-year disease-free survival (DFS) of patients with maximal tumor size (Dmax ≥50 mm) was significantly lower (46.2%) than that for patients with Dmax <50 mm (88%; p <0.0001).
Ebner et al. (136) reported that, in comparing MRI findings in 12 women with recurrent pelvic tumors and 10 with fibrotic mass (confirmed by laparotomy or biopsy in 21 patients), they were able to differentiate the two processes accurately in most instances. However, it is highly desirable to confirm abnormal or suspect lymph node radiographic findings with CT-guided fine-needle aspiration biopsies.
Corn et al. (96) evaluated endorectal coil MRI in 18 patients with cervical carcinoma (stages IB to IIIB); in seven patients, tumors were determined to be in a higher stage by endorectal coil MRI because of proximal vaginal involvement or the combination of proximal vaginal involvement and parametrial extension). Patients were treated with EBRT and low–dose rate (LDR) brachytherapy. Compared with those who had dark or intermediate signal, patients with bright signal characteristics tended to present with earlier stages, were less likely to have anemia, and more likely to have complete response to external irradiation.
Positron Emission Tomography
Positron emission tomography (PET) scanning is increasingly used in the evaluation of patients with malignant neoplasia, including invasive cervical cancer, using 2-[18F]-fluoro-2-deoxy-D-glucose (FDG). Rose et al. (521), in 32 patients with locally advanced carcinoma of the cervix, observed uptake in 91% of the primary tumors. Compared with surgical staging, PET scanning had a sensitivity of 72% and a specificity of 92% in detecting para-aortic metastasis.
Grigsby et al. (207) compared CT and FDG-PET scanning for lymph node staging in 101 patients with carcinoma of the cervix. CT demonstrated abnormally enlarged pelvic lymph nodes in 20 and para-aortic lymph nodes in seven patients, whereas PET demonstrated abnormal FDG uptake in pelvic lymph nodes in 67, in para-aortic lymph nodes in 21 and in supraclavicular lymph node in eight. The 2-year progression-free survival rate, based solely on para-aortic lymph node status, was 64% in CT-negative and PET-negative patients, 18% in CT-negative and PET-positive patients, and 14% in CT-positive and PET-positive patients (p <0.0001). The most significant prognostic factor for progression-free survival was the presence of positive para-aortic lymph nodes on PET imaging (p = 0.025). The authors noted in 76 patients with no abnormal FDG uptake, 2-year survival was 86%, with persistent abnormal uptake 40% and no survivors in patients who developed new sites of abnormal uptake (206). In a follow-up study of 152 patients, the authors reported 5-year cause-specific survival (CSS) of 80% in 114 patients without abnormalities on posttherapy FDG-PET versus 32% in 20 with persistent uptake and no survivors in 18 with new sites of abnormal uptake (205). In another study on 208 patients, Grigsby et al. (208) noted a close correlation between doses of irradiation and number and size of positive lymph nodes with treatment failures and survival (Fig. 66.4).

Hope and Grigsby (257) performed FDG-PET scans in 58 patients with cervical carcinoma who had endometrial biopsy or dilatation and curettage; 36 (64%) had pathologic endometrial invasion (EI). Pelvic lymph node metastasis was more commonly detected in this group than in patients without EI (70% vs. 23%, respectively; p <0.001) as were para-aortic node and supraclavicular node metastasis (30% vs. 0%; p = 0.006). Further, 2-year survival was 78% versus 58% and overall survival 92% versus 65%, respectively (p = 0.047).
Lin et al. (377) described the use of FDG-PET for brachytherapy treatment planning in 24 patients with cervical carcinoma, improving tumor coverage dose distribution, lowering dose to pelvic normal tissues, and improving outcome. Lin et al. (378), using FDG-PET in 32 patients with cervix carcinoma, observed a reduction in physiologic tumor volume of 50% occurring within 20 days from the initiation of radiation therapy.
Staging
The staging recommendations were last revised in 1995. Stage TIB includes all invasive tumors limited to the cervix larger than IA2. Stage TIB occult is no longer used. In 1995, FIGO modified the staging of stage IB lesions (confined to the cervix) into IB1, clinical lesions no >4 cm in size, and IB2, lesions >4 cm in size. There were no changes in the other stages, including the 1987 definitions of stages IA, IA1, and IA2 (553,621).
A parallel TNM staging system has been proposed by the American Joint Committee on Cancer (191). All histologic types should be included. When there is a disagreement regarding the staging, the earlier stage should be recorded (Table 66.6 and Fig. 66.5).
Kolstad (333) reviewed results of therapy in 643 patients with microinvasive carcinoma reclassified as stage IA1 or IA2.
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Three of 232 patients with stage IA1 disease (1.3%) and 12/411 with stage IA2 (2.9%) had local recurrence in addition to four pelvic recurrences, confirming the validity of the staging modification.

The FIGO staging system is based on clinical evaluation (inspection, palpation, colposcopy); roentgenographic examination of the chest, kidneys, and skeleton and endocervical curettage and biopsies. Lymphangiograms, arteriograms, imaging findings, and laparoscopy or laparotomy findings should not be used for clinical staging.
Suspected invasion of the bladder or rectum should be confirmed by biopsy. Bullous edema of the bladder and swelling of the mucosa of the rectum are not accepted as definitive criteria for staging.
For a lesion to be classified as stage IIIB, the tumor should definitely extend to the lateral pelvic wall, although fixation is not required.
Patients with hydronephrosis or nonfunction of the kidney ascribed to extension of the tumor are classified as stage IIIB regardless of the pelvic findings. The currently used staging systems could be modified to accommodate some prognostic factors that have been reported, such as the significance of endometrial extension of cervical carcinoma, stromal invasion, and tumor volume in stage I and IIA carcinoma (barrel-shaped in the cervical or bulky tumor presentations), lymphatic/vascular permeation, and involvement of the lateral parametrium in stage IIB as opposed to the medial parametrium (478,489).
Surgical Staging
Some gynecologists have advocated the use of pretherapy laparotomy, particularly to evaluate the involvement of para-aortic lymph nodes. Recently, sentinel node biopsy in patients with cervical cancer has been used with encouraging results (120). The GOG prospectively evaluated 290 patients with carcinoma of the cervix (346); para-aortic node metastases were found in 19/58 (32.8%) patients with clinical stage IIB and 19/61 (31.1%) with stage IIIB disease.
A number of studies have compared the significance of para-aortic nodal metastases with other clinical and surgical findings with regard to progression-free survival and survival (578). In 626 patients treated on GOG randomized studies, the relative risk associated with positive para-aortic nodes was 11.0 for time to recurrence and 6.2 for survival time. In addition to the significant increase in risk of regional relapses, patients with para-aortic nodal metastasis are more likely to have extrapelvic failure (36).
Ketcham et al. (310) reported positive scalene fat pad biopsies in 7/36 (19%) patients with stage II, III, and IV carcinoma of the cervix and in 4/22 patients with postirradiation recurrences. However, this procedure is no longer routinely carried out at most institutions because of the low yield of positive specimens. Perez-Mesa and Spratt (479) found no supraclavicular node metastasis in 73 consecutive patients with various stages of cervical carcinoma. Manetta et al. (397) also did not detect scalene node metastasis in 24 patients with recurrent
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carcinoma of the cervix evaluated for exploration and possible pelvic exenteration.

Follow-Up
After treatment, patients should be regularly followed by both the radiation and the gynecologic oncologists. Careful history taking and a complete physical and pelvic/rectal examination usually is performed every month for the first 3 months after completion of irradiation, every 3 months for the remaining of the first year, every 4 months the second year, every 6 months during the third through fifth year, and yearly thereafter. The use of Pap smears for cervical and vaginal cytology as a follow-up study is controversial because of bizarre postirradiation cellular morphology that renders it difficult to distinguish postirradiation changes from residual or recurrent malignant cells (400,564). DNA analysis of postirradiation cytologic smears demonstrating atypia or dysplasia may provide ancillary information (109).
Rintala et al. (511) evaluated the reliability of cytologic analysis and atypia after radiation therapy in 89 patients treated for cervical carcinoma. A total of 697 Pap smears were taken; during the follow-up, 44 patients had recurrent disease, which was local in 17 (39%) cases. The rate of false-positive samples was only 3%. Radiation-induced atypia was detected in 28% of the Pap smears taken during the first 4 months after radiation therapy, and its incidence decreased thereafter. In 1,000 patients treated with either surgery or radiation therapy at the M.D. Anderson Cancer Center for stage IB cervical cancer posttreatment, Pap smears did not detect a single asymptomatic recurrence among 133 patients with recurrent disease (41).
The presence of apparently viable tumor cells in the cytologic smear 3 months after irradiation should be evaluated with cervical biopsies, dilation and curettage, and careful examination under anesthesia, as indicated.
Complete blood counts and chemistry profile tests are obtained as clinically indicated. Chest radiography is commonly obtained on a yearly basis, usually for the first 5 years posttreatment, although its value to detect curable lung metastasis is not proven. If radiographs are consistently negative, obtaining them every other year thereafter may be sufficient.
Other imaging studies, such as CT, MRI, PET scanning, or bone scans, are obtained when clinically warranted. When persistent or recurrent tumor is suspected, biopsies should be obtained for histologic confirmation. If a biopsy is positive, immediate treatment should be instituted, as is discussed later.
Usually, hematometra after radiation therapy for cervical carcinoma is related to recurrent disease but occasionally may be related to estrogen replacement therapy, endometrial activity, and fibrosis and obliteration of the endocervix (634).
Pathologic Classification
Over 90% of tumors are squamous-cell carcinoma. Approximately 7% to 10% are classified as adenocarcinoma, and 1% to 2% are the clear-cell, mesonephric type.
Squamous-cell or epidermoid carcinoma is composed of cores and nests of epithelial cells arranged randomly; cells show central keratinization with cornified pearls and sometimes necrosis. Nonkeratinizing tumors may be seen. Electron microscopy may show desmosomes and tonofilaments. Squamous-cell carcinomas are divided into three types: large-cell keratinizing and nonkeratinizing and small-cell type, and they are subdivided according to the degree of differentiation into well, moderately, or poorly differentiated.
Verrucous carcinoma is a variant of a very well-differentiated squamous-cell carcinoma that characteristically has a tendency to recur locally but not to metastasize (338). Mitotic activity is very low. It may be difficult to discriminate from a giant condyloma with cytologic atypia or from a well-differentiated invasive squamous carcinoma. Microscopically, verrucous carcinoma is exophytic, with an undulating, hyperkeratotic surface; the deep margin of a verrucous carcinoma is composed of large, bulbous masses that invade along a wide front in a “pushing” fashion.
Adenocarcinoma arises from the cylindrical mucosa of the endocervix or the mucus-secreting endocervical glands. Mucinous is the most common substage of adenocarcinoma. The endocervical adenocarcinoma may form mucosal glands lined by high columnar cells and produce tubular folds oriented in many directions. In another subtype, cells resemble those of the intestines; the epithelium tends to be pseudostratified and may contain goblet cells. The third variant is the signet-ring cell, which is rare and usually mixed with the endocervical or intestinal patterns.
Endometrioid carcinoma is the most common cell type of endocervical adenocarcinoma; the cells resemble those of the endometrium, and the presence of intracytoplasmic mucin in some cells may be seen in a substantial proportion of tumors. The World Health Organization recommends that endometrioid or endocervical types of adenocarcinoma be graded according to their architecture, based on the degree of gland formation (385).
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Sometimes it is difficult to differentiate a primary endocervical adenocarcinoma from an endometrial tumor. Drescher et al. (126) described a higher incidence of involvement of the uterine corpus and the regional lymph nodes in 21 patients with adenocarcinoma compared with a similar number of patients with squamous-cell carcinoma. Chao et al. (71) and Contag et al. (93) described the use of microarray analysis for gene profiling (cDNA/RNA) to understand the molecular features of these tumors, which could aid in their classification. HPV has been identified in some subtypes of adenocarcinoma of the cervix (16).
A well-differentiated cervical adenocarcinoma has been improperly designated as adenoma malignum when it is truly a malignant tumor that invades adjacent tissues and may produce distant metastasis (559).
Adenosquamous carcinoma is relatively rare (2% to 5%) and consists of intermingled epithelial cell cores with squamous features and glandular structures. The squamous component is frequently nonkeratinizing. If the squamous component is benign metaplasia, the tumor is called adenoacanthoma.
Glassy cell carcinoma (1% to 2%) is considered a poorly differentiated adenosquamous tumor; it is rare and highly malignant. Survival is poor after surgery or irradiation. Ulbright and Gersell (622), in five cases of glassy cell carcinoma evaluated by light and electron microscopy, described both glandular and squamous differentiation. Littman et al. (379) reported only 4/13 patients, the majority with stage II disease, surviving 5 years (six had extrapelvic failures). Piura et al. (485) reported on five patients with cervical glassy cell carcinoma, three with stage IB1. All three patients were alive without disease 4, 12, and 18 months after diagnosis.
Adenoid cystic carcinoma is a rare variant of adenocarcinoma of the cervix (<1%) with an appearance similar to its counterparts in the salivary gland or the bronchial tree (184). The tumor is composed of nests and nodules of small carcinoma cells with a few characteristic cribriform patterns. Immunohistochemical findings for type IV collagen and laminin reveal intercellular cylinders composed of basement membrane material in the solid area without a cribriform pattern. They are locally aggressive and prone to metastasize (444).
Clear-cell carcinoma (mesonephric), not related to DES exposure, comprises approximately 2% of primary cervical adenocarcinomas and is thought to arise in mesonephric remnants (243). These tumors are submucosal, composed of clear and “hobnail” cells, and may grow in a tubular, glandular, papillary, or solid pattern. They appear at any age, with one-third occurring in women younger than 30 years of age. The clear cell is characterized by a voluminous cytoplasm filled with glycogen and the hobnail cell by single-cell apical projections into the neoplastic lumina. These tumors tend to be deeply positioned, with the bulk of the lesion on the stroma forming tubular structures, diffusely infiltrating the cervical stroma.
Clement et al. (89) described the clinicopathologic features in nine patients. Gross examination revealed polypoid or pedunculated masses that invaded the cervical wall in 50% of the hysterectomy specimens. On microscopic examination, five tumors contained basaloid carcinoma or squamous-cell carcinoma and four adenocarcinoma. In seven tumors, the sarcomatous component was homologous, usually resembling fibrosarcoma or endometrial stromal sarcoma, and two tumors contained heterologous sarcomatous elements. Cervical malignant müllerian mixed tumors, compared with their counterparts in the corpus, are more commonly confined at presentation and may have a better prognosis.
Small-cell carcinoma of the cervix, according to some authors, arises from endocervical argyrophilic cells or their precursors, multipotential neuroendocrine cells; however, some small-cell tumors do not contain morphologic evidence of neuroendocrine origin. Nuclear molding, absence of nucleoli, cell necrosis, and high mitotic activity are common. One-third to one-half stain positively for neuroendocrine markers such as chromogranin, serotonin, synaptophysin, or somatostatin. In the majority of patients, the cervical stroma is extensively infiltrated by single small round cells (2). Lymphatic and vascular invasion are significantly more common in small-cell carcinomas (noted in 58% of patients with stage IB disease; 40% of these patients had lymph node metastases at the time of radical surgery) (177). HPV 18 has been detected in the majority of these tumors (273).
Gersell et al. (177) described 15 patients with small-cell carcinoma; 13 showed cytokeratin on immunohistochemical studies, and at least one neuroendocrine marker was found in all 13 tumors (neuron-specific enolase, Leu-7, chromogranin, and synaptophysin). Invasion of vascular spaces was a prominent feature in seven tumors. Only three patients were alive 5, 11, and 78 months after treatment. In contrast, Van Nagell et al. (629), in an analysis of 25 patients, noted a 5-year survival rate of 54% for all stages of small-cell carcinoma, compared with 68% for matched large-cell nonkeratinizing squamous-cell and 74% for keratinizing squamous-cell carcinomas.
Basaloid carcinoma or adenoid-basal carcinoma, an extremely uncommon tumor, is characterized by nests or cords of small basaloid cells, prominent peripheral palisading of cells in the tumor nests, no significant stromal reaction or capillary space invasion, and an infiltrating growth pattern. Some authors have suggested a slow growth pattern with limited local invasiveness and low probability of lymph node metastases (107). Prognosis is excellent (358).
Primary sarcomas of the cervix have been occasionally described (e.g., leiomyosarcoma, rhabdomyosarcoma, stromal sarcoma, carcinosarcoma) (615).
Malignant lymphomas, primary or secondary in the cervix, have been sporadically reported. They behave, are classified, and should be treated as other lymphomas (148).
Metastasis of distant tumors to the uterine cervix are rare (about 4% of all tumors) and should be considered in the differential diagnosis. Metastasis from the breast, ovary, and kidney have been reported (53,464,557).
Prognostic Factors
Patient Factors
Age
According to some reports, age is not a prognostic factor in carcinoma of the cervix (116). Other authors have noted decreased survival in women younger than 35 or 40 years (108), who have a greater frequency of poorly differentiated tumors. In contrast, two European studies showed improved outcome for younger patients (407). This apparent contradiction may be explained by an analysis by Rutledge et al. (537), who showed an interaction between age and stage in the relative hazard plots for 250 patients younger than 35 years of age and matched control subjects. Mitchell et al. (413) evaluated 398 patients with stage I to III cervical carcinoma treated with radiation therapy. Patients were divided into nonelderly (35 to 69 years of age; n = 338) and elderly (≥70 years of age; n = 60) groups. Comorbid conditions in the elderly resulted in diminished ability to undergo intracavitary brachytherapy. Although the 5-year actuarial disease-free and CSS rates were comparable in the two groups, tumor recurrence and death from cervical cancer were more common beyond 5 years in the elderly group.
Race/Socioeconomic Status
Several authors have noted a correlation between racial or socioeconomic characteristics of patients and outcome of
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therapy (78,648). Mundt et al. (427) examined factors affecting outcome in 316 African American and 94 white patients undergoing RT for cervical cancer. With a median follow-up of 72.4 months, African Americans had a trend toward poorer 8-year cause-specific survival rates (47.9% vs. 60.6%; p = 0.10) compared with white patients. Factors correlating with poor outcome, present in the African American group, included lower hemoglobin (Hb) levels during RT (p = 0.001), lower median income (p = 0.001), and less frequent intracavitary brachytherapy (p = 0.09). Multivariate analysis demonstrated that race was not an independent prognostic factor after controlling for difference in patient, tumor, and treatment factors. Grigsby et al. (195), in 452 white and 124 African American women with stage II or III cancer of the cervix treated with RT alone, observed 5-year CSS rates for stage II of 66% and 61% (p = 0.56) and for stage III 38% and 47% (p = 0.34), respectively. Overall survival rates for stage II for the two racial groups were different (60% and 51%, respectively; p = 0.02) and may be related to non–cancer-related comorbidity factors.
Brooks et al. (56) evaluated 1,009 patients with invasive carcinoma of the cervix; 606 white, 354 African American, and 5% “other” races. African Americans were more likely to have Medicaid or to be uninsured (44% vs. 23%; p = 0.001) and were more likely to be admitted for an emergency or for a cancer-related complication (p = 0.036), to have comorbid illness (p = 0.001), to be admitted for a transfusion (p = 0.01), or to be treated with irradiation rather than surgery (p = 0.001). Racial differences existed in patterns of admission, type of therapy, and severity of illness.
Moreover, in an analysis of the 1994 Patterns of Care study of 471 cases of squamous-cell carcinoma treated in the United States and a randomly selected 215 additional cases from 17 institutions that admitted more than 40% minority patients, women who lived in low-income neighborhoods, who had only Medicaid coverage, or who were treated at large academic or minority-rich institutions tended to have a poorer initial performance status, higher-stage or bulky central tumor, and a lower pretreatment hemoglobin level (303).
General Medical Factors
Anemia and Tumor Hypoxia
Although stage, tumor volume, histologic type of the lesion, and vascular or lymphatic invasion are known to affect the prognosis of patients with cervical carcinoma, hemoglobin levels have also been the subject of extensive investigation in this regard.
Reviewing experimental data, Hirst (249) emphasized that in animal tumor models the opportunity to affect radiosensitivity by blood transfusion is transient. Blood transfusion is in general beneficial to the anemic patient with cancer, but it must be given as soon as possible before the first radiation dose to maximize its effects. Accounting for both the normal pulmonary and peripheral circulation and parallel flow through tumor tissue, Kavanagh et al. (308) calculated that decreasing hemoglobin–oxygen affinity should render a quantitatively greater decrease in radiobiologically hypoxic regions than what has been measured after the use of transfusions alone (586).
Using polarographic needle electrodes for direct tumor tissue oxygen measurements, investigators have reported worse outcomes for patients whose tumors have either a median partial pressure of oxygen (PO2) level below 10 mm Hg (251) or a high percentage of PO2 measurements below 5 mm Hg (330,518). Comparisons of intratumoral oxygen measurements before and after external-beam radiation therapy have usually indicated a trend toward improved oxygenation after radiation therapy (94,129), but the significance of posttreatment measurements is unclear (169). Hypoxic tumors are more likely to recur locoregionally than well-oxygenated tumors regardless of whether surgery or radiation therapy is the primary local treatment (251).
Höckel et al. (251) reported higher 5-year disease-free survival rates in 21 patients in whom median oxygenation measured with polarographic needle electrodes was at least 10 mm Hg, in contrast to only 40% in 23 patients with a PO2 <10 mm Hg.
Hypoxia-mediated genetic alterations such as inactivation or mutation of p53 are suspected to impart biologically aggressive traits (186).
Haensgen et al. (217), in 70 patients with stage IIB to IVA cervical cancer treated with EBRT and brachytherapy, analyzed biopsies for p53 transformed with a functionally inactive mutation (tp53) and DNA index measured by flow cytometry. In vivo oxygenation was measured with an Eppendorf probe, and patient hemoglobin levels were recorded. Patients with hemoglobin <11 g/dL had a 3-year survival rate of 27%, compared with 62% in those with hemoglobin ≥11 g/dL (p = 0.006). Of 70 tumors, 49 showed evidence of hypoxia (any reading of PO2 <5 mm Hg) and a trend toward poorer survival compared with nonhypoxic tumors (48% vs. 70%; p = 0.07). Sixty of 70 tumors showed tp53 expression, which alone had no impact on survival (tp53 = 50% vs. wtp53 = 79%; p = 0.11). Hypoxic tumors had a significantly higher expression of tp53 (p = 0.012), whereas FIGO stage and anemia had no impact on p53 expression. Combining hypoxia and tp53 allowed stratification of subgroups with differing 3-year survival rates: tp53 (n = 10), 79%, and tp53 without hypoxia (n = 44), 47%. Flow cytometry demonstrated no effect of ploidy on survival. Advanced stage and pretreatment hemoglobin are independent prognostic factors in cervical carcinoma. Mutated or transformed tp53 was found more often in hypoxic tumors.
Notwithstanding the uncertain association between hypoxia and anemia, a randomized trial reported by Bush (64) 20 years ago remains an influential study; 132 patients with stage IIB to III cervical cancer were randomized to a control arm in which transfusions were given only if the hemoglobin level dropped below 10 g/dL, or an experimental arm in which transfusions were given to maintain the hemoglobin level at or above 12.5 g/dL. The results in the initial report suggested an improved outcome for patients in the experimental arm who received transfusion, but Bush underscored the need to interpret the study results with caution in view of certain inherent biases in the analysis. As noted by Fyles et al. (168), there was not a statistically significant difference in outcome between treatment arms when compared by an intent-to-treat analysis. Second, the randomization was not stratified according to the potentially confounding influence of tumor size, and records of individual patients' tumor dimensions are not available. Finally, and perhaps most important, the thresholds for transfusion were based on anemia during therapy, not the initial hemoglobin. Although the subgroup analysis indicated a difference between patients in the control arm who received transfusion and patients in the experimental arm who received transfusion, only the least responsive patients in the control arm would likely continue to bleed during treatment and require a transfusion for a hemoglobin decrease below 10 g/dL, whereas the higher threshold for transfusion in the experimental group would have captured more patients already beginning to respond early in the course of treatment. Subsequently, Thomas (606) reviewed the Canadian experience and found that in 605 eligible patients with cervical cancer, 25% received blood transfusions, most frequently when Hb was below 100 g/L. On multivariate analysis baseline Hb was not a significant prognostic factor, but average weekly nadir during radiation therapy was significant (those with values higher than 120 g/L had lower incidence of local relapses and distant metastasis and better 5-year survival than patients with lower Hb levels).
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Dunst et al. (130) studied 87 patients with squamous-cell cervical carcinoma treated with EBRT and HDR brachytherapy. Tumor oxygenation was measured with Eppendorf PO2 before RT and at 19.8 Gy and angiogenesis was determined by microvessel density on biopsies. Pretreatment anemia had a significant impact on relapse rate (at 3 years, 6% in 20 patients with Hb >13 g/dL, 15% in 47 with Hb between 11to 13 g/dL and 67% in 20 with Hb <11 g/dL). The 3-year overall survival was 79%, 64%, and 32%, respectively). Twenty-three tumors were poorly oxygenated (median PO2 <15 mm Hg before RT and at 19.8 Gy) and 3-year survival was 38%, compared to 68% in patients with higher PO2 (p = 0.02).
On the other hand, Eifel et al. (139), in a retrospective review of 2,997 patients with cervical cancer stage I or II treated with RT, found no impact of any Hb parameter on central, pelvic, or distant failures. Only tumor size and lymph node status were independent predictors of central recurrence (p <0.0001) and tumor size, FIGO stage, lymph node status, and marginally transfusion during RT (p = 0.04) were correlated with disease-specific survival.
Munstedt et al. (426), in 183 patients who received adjuvant postradical surgery RT, noted that those with Hb <11 g/dL had lower recurrence-free and overall survival. Noteworthy, the difference was present mainly in a subgroup of women who had inadequate surgery.
The issue of whether blood transfusions to hemoglobin levels above 12 to 12.5 g/dL improve prognosis remains unsettled, but there are additional data to support that giving transfusions to maintain the average hemoglobin level during treatment at that level is beneficial. In a retrospective review of over 600 patients treated at seven different cancer centers in Canada, Grogan et al. (212) observed that the patients who maintained an average weekly hemoglobin level above 12 g/dL with or without transfusions had a significantly higher 5-year survival rate than patients with lower average weekly hemoglobin levels, regardless of the hemoglobin at presentation.
Many radiation oncologists routinely administer red blood cell transfusions (RBCT) to correct anemia before treatment with radiation therapy for cervical cancer, hoping at least for a generally favorable effect on the patient's sense of well-being and energy level if not also an impact on tumor radiosensitivity. Kapp et al. (297) reported on 204 patients who received red cell transfusion during RT when Hb level was <11 g/dL. Patients whose Hb was corrected (18.5%) had outcome similar to nontransfused patients. However, patient nonresponders to RBCT had decreased tumor control and survival.
Vaupel et al. (633), in a review of published data, concluded that maximum oxygenation of tumors is expected with Hb in the range of 12 to 14 g/dL for women and that higher Hb levels may not be better. This has implications for transfusions or administration of epoetin.
During the past decade, it has been established that recombinant human erythropoietin (EPO) provides an alternative means of sustaining or raising hemoglobin levels during radiation therapy. Typically, a dose of 200 U/kg per day 5 days per week would be expected to elevate hemoglobin by an average of 1 to 3 g/dL (133,356,637).
Dusenbery et al. (133), in 20 patients with carcinoma of the cervix with anemia, noted that EPO induced a prompt reticulocyte response (from 2.4% to 4.9%) by the beginning of radiation therapy. In the EPO group, the mean baseline hemoglobin level was 10.3 g/dL; by the second week it had increased to 12.2 g/dL, and by completion of radiation therapy, to 13.2 g/dL. Mean baseline hemoglobin level in concurrent control patients was 10.7 g/dL; at the completion of radiation therapy it was 10.4 g/dL.
Although it is clear that EPO can reduce the need for transfusions for anemic patients with cancer in a variety of settings, its effect on quality of life is less certain (547). Furthermore, there is currently no proof that the use of EPO is in any way superior to transfusions with respect to impact on clinical outcome for patients receiving radiation therapy in particular, and transfusions are a less expensive option in most cases (305).
Other Medical Factors
Jenkin and Stryker (280) observed a higher incidence of pelvic recurrences and complications in patients with arterial hypertension (diastolic pressure >110 mm Hg).
Kapp and Lawrence (296) reported on 398 patients; patients with temperatures over 101°F had a higher incidence of distant metastases and a lower survival rate.
Tumor Factors
Tumor Volume
There is a close correlation between depth of stromal invasion, tumor size, and incidence of parametrial and pelvic node metastases and survival in patients with cervical cancer (12,117). In a study of women treated with radical hysterectomy, the 5-year disease-free survival rate was 90% in 181 patients stage IB1 (≤4 cm) and 72.8% in 48 patients with stage IB2 disease (p = 0.02) (155).
Toita et al. (614), in a review of 70 patients with stage IIB and IIIB carcinoma of the uterine cervix treated with RT alone, reported no significant correlation of 5-year DFS with size of the cervical tumor <60 mm (70% to 85%); however, in patients with tumor >60 mm, the 5-year DFS was 28.6%.
Piver and Chung (488) showed a greater incidence of lymphatic and distant metastasis and lower survival rates in patients with bulky and barrel-shaped stage IB and IIA tumors treated by radical hysterectomy (Table 66.7). Also, a higher incidence of pelvic recurrences and distant metastases and a decreased survival rate were reported by Fletcher (161), Eifel et al. (142), and Perez et al. (476) in patients with larger tumors treated with irradiation. In stages IB and IIA, higher radiation doses or combination with an extrafascial hysterectomy improved local tumor control (144,474).
Further, Leveque et al. (375), in patients with stage I to II adenocarcinoma of the cervix treated with RT alone or combined with radical surgery, noted that FIGO stage and pelvic node involvement were the most important parameters influencing overall survival. Silver et al. (558), in 93 patients with stage I adenocarcinoma of the cervix, described patient age and tumor grade as significant prognostic variables for survival (p <0.01 and 0.01, respectively); tumor size was significant (p <0.01) for survival and progression-free survival.
In contrast, Grigsby et al. (198), in patients with stage IB and IIA carcinoma of the cervix treated with preoperative irradiation and radical or conservative hysterectomy, observed no correlation of tumor volume with outcome. The 5-year pelvic failure rates for stage IB were 16% for tumors smaller than 3 cm and 9% for larger tumors (p = 0.90) and for stage IIA 22% for tumors both smaller or larger than 3 cm (p = 0.75).
Several retrospective studies have demonstrated decreased survival and a greater incidence of distant metastases in patients with endometrial extension of a primary cervical carcinoma (endometrial stromal invasion or replacement of the endometrium by tumor only) (470). Grimard et al. (211), on the other hand, confirmed these findings only in patients with stage IB tumors, but not in more advanced stages. Similar findings were noted by Noguchi et al. (445). Patients without uterine body invasion had a 5-year survival rate of 92.4% compared with 53.8% in patients with invasion.

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Histology
Most reports have shown no significant correlation of survival or tumor behavior with the degree of differentiation of squamous-cell carcinoma or adenocarcinoma of the cervix (10,79,640).
Alfsen et al. (10) analyzed 417 adenocarcinomas and 88 other nonsquamous-cell carcinomas of the cervix; in patients with stage I, histological type, extension to the vagina or corpus uteri, tumor volume (>3,000 mm3), infiltration depth (in thirds of the cervical wall), vascular invasion, lymph node metastases, treatment, and patient age were significant prognostic variables.
Although Reagan and Fu (507) demonstrated prognostic value of histologic differentiation in patients treated with irradiation, Crissman et al. (101) failed to observe a correlation between histologic parameters and patient survival.
Angiogenesis and Tumor Vascularity
Microvessel count is higher in patients with cervical neoplasia than in control patients and higher in patients who experience posttreatment recurrences. Obermair et al. (448), in 166 patients with stage IB cervical cancer, observed a 5-year survival rate of 89.7% in 102 patients whose tumors had a microvessel density of 20/field or less and 63% in 64 patients whose tumors had a microvessel density of >20/field (log rank p <0.0001). Similar findings were reported by Cooper et al. (95).
Loncaster et al. (383), in a retrospective study of 100 patients, found that vascular endothelial growth factor (VEGF) expression in tumor biopsies in advanced carcinoma of the cervix was associated with a poor prognosis.
Flow Cytometry Studies on DNA and Growth Fraction
Some authors have noted no significant difference in recurrence rates between patients with diploid or aneuploid tumors. Kristensen et al. (339), in a study 465 patients with invasive carcinoma of the uterine cervix on whom DNA index and S-phase fraction studies were performed, observed that neither ploidy level nor S-phase fraction had prognostic significance. On the contrary, Strang et al. (582) noted more relapses in tumors with an S-phase rate of 20% or greater.
Apoptosis and Radiation Response Markers
Wheeler et al. (652) evaluated levels of apoptosis as “predictors for tumor response” in 44 patients with stage IB adenocarcinoma of the cervix. Patients whose tumors had a baseline apoptosis level above the median value (2%) had better overall survival than those with lower than median levels (p = 0.056). Chung et al. (86), in pretreatment biopsy specimens of 48 patients with stage IIB squamous-cell carcinoma of the uterine cervix treated with RT, found that those tumors with an apoptotic index above the median had better tumor control (p = 0.0062) and overall survival (p = 0.0053) than those whose tumors had a lower apoptotic index. Sheridan et al. (555), in a study of 39 patients with adenocarcinoma of the cervix, also noted that when the apoptotic index was quantified, the 5-year survival rates for women with tumors whose apoptotic index/mitotic index was greater or less than the median were 81% and 25%, respectively.
On the other hand, Paxton et al. (465) examined the percentage of apoptotic cells in 146 carcinomas of the cervix from patients scheduled to receive RT. The median apoptotic level was 0.73%. Patients were divided into two groups around the median. There was no statistically significant difference in outcome between the two groups.
Cerciello et al. (69), in 40 patients with stage IIA-IIIB cervix cancer treated with RT without chemotherapy, obtained biopsies before and after five fractions of RT. They observed significant changes in the cell cycle of cervical cancer, indicating intact G2/M checkpoint function, leading to the expectation that targeting compounds interfering with G2/M transition may enhance the effect of irradiation on cervix cancer.
Tsang et al. (619), in patients with carcinoma of the uterine cervix treated with irradiation, observed that the most significant factors for disease-free survival were large tumor size (p = 0.01), low hemoglobin (p = 0.01), labeling index (LI) flow cytom-etry (disease-free survival 67% for LI lower than 7%, 33% for LI of 7% or higher; p = 0.03), and potential doubling time (T(pot)) (66% for T(pot) longer than 5 days, 35% for T(pot) of 5 days or less; p = 0.04). For small tumors (<6 cm in diameter), either a high LI (>7%) or a high apoptotic index (>1%) were associated with poorer disease-free survival.
West et al. (650) evaluated the intrinsic radiosensitivity of 145 tumor biopsies from patients with cervical carcinoma (in vitro survival fraction at 2 Gy using a clonogenic assay). Diploid tumors tended to be more radioresistant than aneuploid tumors (p = 0.07).
Bax, Bcl-2, c-erbB-2, p53
Bax protein serves as a positive regulator of apoptosis by forming heterodimers with bcl-2 protein, promoting cell survival; c-erbB-2 is a cell growth factor, and p53 a tumor suppressor gene. Ohno et al. (452) assessed the relation between apoptosis and the expression of Bax and Bcl-2 protein during RT for cervical carcinoma in 20 patients before and after administration of 9 Gy. The apoptotic cell index in tumor cells was 0.22% before irradiation and 1.20% after 9 Gy (p = 0.0004). The positive rate of Bax protein increased from 15% (in 3/20 patients) before irradiation to 60% (in 12/20 patients) after 9 Gy (p = 0.0126), suggesting that Bax protein is associated with apoptosis induced
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by fractionated radiation therapy. Wootipoom et al. (663), in 174 patients with cervical cancer, noted Bax, Bcl-2, and p53 expression in 68.4%, 25.9%, and 77.6% of the cases, respectively. Bax expression was associated with better survival, whereas Bcl-2 expression was associated with poor survival. Jain et al. (277) also found that neither Bcl-2 nor p53 expression were independent predictors of outcome in locally advanced cervical cancer.
Grace et al. (185), in a study of 105 patients with cervical cancer and 20 age-matched controls, noted a highly significant correlation between p53 and Bcl-2 expressions and HPV infection (p = 0.00001) and with various stages from dysplasia to invasive carcinoma.
Harima et al. (233), in 37 patients with stage IIIB cervical carcinoma treated with irradiation alone or combined with hyperthermia, noted that pelvic tumor control was associated with increased Bax expression: 10.5% (2/19) in the RT group versus 44.4% (8/18) in the thermoirradiation group (p = 0.02).
Mukherjee et al. (425) retrospectively analyzed 78 cases of stage II or IIB carcinoma of the cervix treated with RT followed by surgery 4 to 6 weeks later. On histologic examination of the surgical specimens, 40 cases (51%) showed a complete response to therapy. In the radioresistant cases, 15% (six cases) had positivity for Bcl-2 and p21 proteins, respectively, and 34% (13 cases) showed mutant p53 protein. None of the radiosensitive tumors were positive for these proteins. Seventy-five percent of the radiosensitive tumors (30 cases) were positive for the Bax antibody, whereas 81% of the radioresistant tumors (31 cases) were negative for Bax (p < 0.01). The presence of Bcl-2, p21, and p53 proteins could also be related to radioresistance of the tumors.
Altered expression of c-ercB-2 protein was shown to have prognostic significance in adenocarcinoma but not in squamous-cell carcinoma of the cervix (396).
The p53 gene controls entry into the S-phase of the cell cycle. Kainz et al. (292), in a study of 109 surgically treated patients, and Ebara et al. (135), in 46 patients with stage IIIB squamous-cell carcinoma of the cervix treated with RT alone, noted no significant difference in outcome, when correlated with p53 protein expression.
Cellular Oncogenes
Alterations in either the expression or function of cellular genes that control cell growth and differentiation have been investigated as prognostic markers in cervical cancer, but, as yet, the data based on small studies show no clear-cut useful marker.
The p27/Kip1 gene inhibits a variety of cyclin-dependent kinase complexes and regulates cell growth. Oka et al. (453) studied 202 biopsy specimens obtained from 77 patients with squamous-cell carcinoma of the cervix before and during RT for expression of p27 and p53 proteins. A high p27 LI before radiation therapy was associated significantly with good disease-free and metastasis-free survival rates. A high p53 LI before irradiation was associated with poor overall survival.
Both specific point mutations and amplification of ras genes have been noted, and overexpression of the ras gene p21 product is associated with a poor prognosis and increased frequency of lymph node involvement (237). Although loss of heterozygosity of the c-Ha-ras gene in squamous-cell carcinomas was not associated with advanced-stage disease, mutations were associated with a poor prognosis. In contrast, mutations of the Ki-ras gene have been detected in a small percentage of cervical adenocarcinomas, but have not been significantly associated with stage, grade, or survival (335,365).
The c-myc oncogene is amplified from three to 30 times in approximately 20% of squamous-cell carcinomas and is more frequent in high-stage compared with low-stage tumors. Overexpression of c-myc has been associated with a worse clinical outcome (275,512).
Gadd45 belongs to the class II family of DNA damage-inducible genes, and its role in DNA repair has been proved in many experimental models. Santucci et al. (543), in 14 patients with cervical cancer, found a correlation between the lack of gadd45 induction and a clinical response to irradiation (both local tumor control and disease-free survival) when a dose ranging from 18 to 25 Gy was delivered to the pelvis.
CD 34 is an antigen present in hemopoietic progenitor cells and is a sensitive marker for endothelial cells. In 62 patients with cervical cancer evaluated by Vieira et al. (636), CD 34 reactivity and higher microvessel density was associated with squamous-cell carcinoma.
CD 109 is a cell surface protein that was found to be expressed in cervical cancer more than in endometrial adenocarcinoma (669), which may have implications for development of new targeted therapy for cervical cancer.
Preoperative elevated CA 125 levels (cutoff value, 26 U/mL) were associated with depth of stromal invasion, lymphovascular invasion, and nodal metastasis in 116 patients with adenocarcinoma of the cervix. In patients with negative nodes, high CA 125 levels determined poor histopathological prognostic factors (618).
Carcinoembryonic Antigen
Tsai et al. (617) in 117 patients with adenocarcinoma of the cervix, 28 of whom had preoperative carcinoembryonic antigen (CEA) levels >5 ng/mL, noted a correlation with larger tumor size, deeper cervical invasion, and lymphovascular invasion (p <0.001). A Spanish study of 96 patients with invasive carcinoma of the cervix and seven with intraepithelial neoplasia showed elevated CEA levels in 33%, CA 19.9 in 32%, and CA 125 in 21.5% of patients (48). Specificity for each tumor maker was 98%. Increased CEA and CA 19.9 levels were found with more advanced stages of the disease and in patients with adenocarcinoma compared with squamous-cell carcinoma. At follow-up, all cases of progressive tumor or recurrence were detected by elevation of one of the three antigens. Specificity during follow-up was 92% for CEA and CA 125 and 92.6% for CA 19.9.
Cytokeratin Markers
In 80 patients with carcinoma of the cervix, expression of cytokeratin 10 and 13 and involucrin was found in 24%, 64%, and 53%, respectively (626). There was no difference in the expression of cytokeratin or involucrin between patients with positive or negative lymph nodes, although in the lymph node–positive group, survival was higher in patients lacking cytokeratin 13 expression (p = 0.02).
In another study of 272 patients with invasive carcinoma of the cervix with 1,053 samples, Bolli et al. (44) noted an elevation of squamous-cell carcinoma antigen (SCC-Ag) before treatment in 53% of 103 patients, increasing with advancing tumor stage at diagnosis. In 70 patients with recurrent tumor, 81% had elevated SCC-Ag. Ngan et al. (442) also identified elevation of serum SCC-Ag in 62% of 308 women with carcinoma of the cervix. Posttreatment SCC levels were raised in 69 patients (22.4%), and this was associated with a <5% 5-year survival rate, in contrast to 87% in women with normal SCC-Ag levels.
Hong et al. (254), in 401 patients with stage I to IV squamous-cell carcinoma of the cervix treated with RT, noted that the preirradiation SCC-Ag level strongly correlated with disease stage. A persistently elevated SCC-Ag level 3 months after RT was a stronger predictor for treatment failure than residual induration by pelvic examination, and it was associated with a higher incidence of distant metastasis.
Likewise, Micke et al. (409), in 141 patients with cervical cancer treated with RT, noted the pretherapy serum level of SCC-Ag was elevated in 72% (>2 ng/mL). Patients with a SCC
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below 7.2 U/mL had better tumor response than those with higher levels. After RT, 98% of patients in complete remission and 87% of those in partial remission had a serum level below the cutoff. In recurrent tumors, 82% of patients had a significant increase in serum levels before clinical manifestation of relapse (≤0.001). Hong et al. (256), in 1,031 patients with squamous-cell cervical cancer treated with RT with or without chemotherapy, noted that independent risk factors for local relapse were advanced stage and age <45 years; 5-year local relapse-free survival was higher (90%) if squamous-cell carcinomas antigen was less than two. This antigen may be a useful marker in the prognosis of patients with carcinoma of the uterine cervix.
Epstein-Barr, Transforming Growth Factor, β-Integrin, and Other Markers
Activity of Epstein-Barr virus antigen–specific killer T cells and shedding of Epstein-Barr virus were evaluated in 55 patients with carcinoma of the cervix (326). Activity was decreased in patients with cervical carcinoma compared with control patients; it became increasingly lower as the clinical stage of the disease advanced, and activity after treatment was clearly related to patient survival. These data may indicate an imbalance in local immunity against viral infection and impairment of T-cell immunity in patients with advanced cervical carcinoma.
In 79 patients undergoing radiation therapy for carcinoma of the cervix, pretreatment transforming growth factor-β1 (TGF-β1) levels were a significant prognostic factor for survival and local tumor control. There were weak significant correlations of TGF-β1 levels with disease stage and the levels of circulating tumor markers (CA 125) (121). Hazelbag et al. (238) also assessed TGF-β1 and plasminogen activator inhibitor (PAI-1) expression in 108 specimens of cervical carcinoma and noted that TGF was not associated with worse prognosis, whereas PAI-1 was.
Gruber et al. (213), in biopsies of 82 patients with cervical cancer, found that β3-integrin was expressed in 50 (61%) and correlated it with higher incidence of locoregional recurrences and decreased survival.
Cyclooxigenases
Gaffney et al. (172), in 24 patients with carcinoma of the cervix treated with RT, observed that 5-year overall survival rates for tumors with low versus high COX-2 values were 75% and 35%, respectively (p = 0.021). COX-2 staining intensity was found to correlate positively with tumor size (p = 0.022).
Kim et al. (322) screened 84 patients with stage IIB squamous-cell and 21 with adenocarcinoma cervical cancer and found COX-2 expression more frequently in the adenocarcinoma group (57% vs. 24%; p = 0.007). The 5-year survival rate was 83% for COX-2 negative and 57% for COX-2 positive patients, regardless of histological subtype (p = 0.001). Pyo et al. (503) also showed that expression of COX-2 and coexpression of COX-2 and thymidine phosphorylase (TP) were correlated with high locoregional recurrence and lower survival. Moreover, Kang et al. (294), in 84 patients with cervix adenocarcinoma, observed a higher incidence of lymph node metastasis and decreased survival with elevated expression of COX-2
Hormonal Receptors
Suzuki et al. (590) investigated the expression of estrogen receptors and progesterone receptors (PgR) in biopsy specimens from cervical tumors before RT in 44 patients with cervical adenocarcinoma and 22 with adenosquamous-cell carcinomas treated. Staining for estrogen receptors or PgR was positive in 12 patients (19%). The estrogen receptor status did not correlate with the local tumor control, disease-free, or cause-specific survival. Disease-free survival rate of PgR-positive patients was significantly higher than that of PgR-negative patients (p = 0.044), but it was not statistically significant in relation to 5-year cause-specific survival or local tumor control.
HIV
In 120 patients with cervical cancer screened for HIV and treated with RT, Campbell et al. (68) observed a 4.2% positive HIV. These patients had more advanced tumors and duration of remission was shorter than in the HIV negative group. RT had no effect on the HIV titers. Women who are HIV positive or have acquired immunodeficiency syndrome associated with in situ or invasive carcinoma of the cervix are at a higher risk for tumor recurrence after treatment and death as a consequence of the malignant process (328,665).