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![]() | PDQ® |
Anal cancer is an often curable disease. The 3 major prognostic factors are site (anal canal versus perianal skin), size (primary tumors less than 2 centimeters in size have a better prognosis), and differentiation (well-differentiated tumors are more favorable than poorly differentiated tumors).
Anal cancer is an uncommon malignancy, accounting for only a small percentage (4%) of all cancers of the lower alimentary tract. Clinical trials have evaluated the roles of chemotherapy, radiation therapy, and surgery in the treatment of this disease.[1,2] Refer to PDQ and to CancerNet (http://cancernet.nci.nih.gov) for information on clinical trials.
Overall, the risk of anal cancer is rising, with data suggesting that male homosexuals, in particular, are at increased risk of anal cancer.[3]
References:
Squamous cell (epidermoid) carcinomas make up the majority of all primary cancers of the anus. The important subset of cloacogenic (basaloid transitional cell) tumors constitute the remainder. Adenocarcinomas from anal glands or fistulae formation and melanomas are rare. Treatment of anal melanoma is not included in this summary.
The anal canal extends from the rectum to the perianal skin and is lined by a mucous membrane that covers the internal sphincter. The following is a staging system for anal canal cancer that has been described by the American Joint Committee on Cancer (AJCC) and the International Union Against Cancer.[1,2] Tumors of the anal margin (below the anal verge and involving the perianal hair-bearing skin) are classified with skin tumors.
-- TNM definitions --
Primary tumor (T)
TX: Primary tumor cannot be assessed
T0: No evidence of primary tumor
Tis: Carcinoma in situ
T1: Tumor 2 cm or less in greatest dimension
T2: Tumor more than 2 cm but not more than 5 cm in greatest dimension
T3: Tumor more than 5 cm in greatest dimension
T4: Tumor of any size that invades adjacent organ(s), e.g., vagina,
urethra, bladder (involvement of the sphincter muscle(s) alone is not
classified as T4)
Regional lymph nodes (N)
NX: Regional lymph nodes cannot be assessed
N0: No regional lymph node metastasis
N1: Metastasis in perirectal lymph node(s)
N2: Metastasis in unilateral internal iliac and/or inguinal lymph node(s)
N3: Metastasis in perirectal and inguinal lymph nodes and/or bilateral
internal iliac and/or inguinal lymph nodes
Distant metastasis (M)
MX: Distant metastasis cannot be assessed
M0: No distant metastasis
M1: Distant metastasis
-- Stage 0 --
Stage 0 anal cancer is carcinoma in situ. Rarely diagnosed, it is a very early
cancer that has not spread below the limiting membrane of the first layer of
anal tissue. Stage 0 anal cancer corresponds to the following TNM grouping:
Tis, N0, M0
-- Stage I --
Stage I anal cancer is cancer that is 2 centimeters or less in greatest
dimension and that has not spread anywhere else. There is no sphincter
involvement. Stage I anal cancer corresponds to the following TNM grouping:
T1, N0, M0
-- Stage II --
Stage II anal cancer is cancer that is more than 2 centimeters and that does
not involve adjacent organs or lymph nodes. Stage II anal cancer corresponds
to the following TNM groupings:
T2, N0, M0
T3, N0, M0
-- Stage IIIA --
Stage IIIA anal cancer is cancer that has spread to perirectal lymph nodes or
to adjacent organs. Stage IIIA anal cancer corresponds to the following TNM
groupings:
T1, N1, M0
T2, N1, M0
T3, N1, M0
T4, N0, M0
-- Stage IIIB --
Stage IIIB anal cancer is cancer that has spread to internal iliac and/or
inguinal nodes (unilateral or bilateral) or has spread to both adjacent organs
and perirectal lymph nodes. Stage IIIB anal cancer corresponds to the
following TNM groupings:
T4, N1, M0
Any T, N2, M0
Any T, N3, M0
-- Stage IV --
Stage IV anal cancer is cancer that has spread to distant lymph nodes within
the abdomen or to other organs in the body. Stage IV anal cancer corresponds
to the following TNM groupings:
Any T, Any N, M1
References:
Abdominoperineal resection leading to permanent colostomy was previously thought to be required for all but small anal cancers below the dentate line, with approximately 70% of patients surviving 5 or more years in single institutions,[1] but such surgery is no longer the treatment of choice.[2,3] Radiation therapy alone may lead to a 5-year survival rate in excess of 70%, although high doses (6,000 cGy or greater) may yield necrosis or fibrosis.[4] Chemotherapy concurrent with lower-dose radiation therapy has a 5-year survival rate in excess of 70% with low levels of acute and chronic morbidity, and few patients require surgery for dermal or sphincter toxic effects.[5-10] The optimal dose of radiation with concurrent chemotherapy to optimize local control and minimize sphincter toxic effects is under evaluation but appears to be in the 50 Gy to 60 Gy range.[11,12] Analysis of an intergroup trial that compared radiation therapy plus fluorouracil/mitomycin with radiation therapy plus fluorouracil alone in patients with anal cancer has shown improved results (lower colostomy rates and higher colostomy-free and disease-free survival) with the addition of mitomycin.[13] Radiation with continuous infusion of fluorouracil plus cisplatin is also under evaluation.[14,15] Standard salvage therapy for those patients with either gross or microscopic residual disease following chemoradiotherapy has been abdominoperineal resection. Alternately, patients may be treated with additional salvage chemoradiotherapy in the form of fluorouracil, cisplatin, and a radiation boost to potentially avoid permanent colostomy.[13]
Because of the small number of cases, information that can only come from patient participation in well-designed clinical trials is needed to improve the management of anal cancer. Patients with stages II, III, and IV disease should be considered candidates for clinical trials.
The tolerance of patients with human immunodeficiency virus (HIV) and anal carcinoma to standard fluorouracil/mitomycin chemoradiation is not well defined.[16,17] Patients with pretreatment CD4 counts of less than 200 may have increased acute and late toxic effects;[18] chemoradiation doses may require modification in this subset of patients.
The designations in PDQ that treatments are "standard" or "under clinical evaluation" are not to be used as a basis for reimbursement determinations.
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Treatment options:
Surgical resection is used for treatment of lesions of the perianal area not involving the anal sphincter (approach depends on the location of the lesion in the anal canal).
Stage I anal cancer was formerly treated with abdominoperineal resection. Current sphincter-sparing therapies include wide local excision for small tumors of the perianal skin or anal margin, or definitive chemoradiation (fluorouracil and mitomycin) for cancers of the anal canal. Salvage chemoradiotherapy (fluorouracil and cisplatin plus a radiation boost) may avoid permanent colostomy in patients with residual tumor following initial nonoperative therapy.[1] Radical resection is reserved for patients with incomplete responses or recurrent disease. Therefore, continued surveillance with rectal examination every 3 months for the first 2 years and endoscopy/biopsy when indicated after completion of sphincter-preserving therapy is important.
Treatment options:
2. All other stage I cancers of the anal canal that involve the anal sphincter or are too large for complete local excision are treated with external beam radiation therapy with or without chemotherapy.[1,3-8]
Chemotherapy with fluorouracil and mitomycin combined with primary radiation therapy appears to be more effective than radiation therapy alone.[9] The optimal dose of radiation with concurrent chemotherapy is under evaluation.[10-12]
Selected tumors are also suitable for interstitial irradiation.[4]
3. Radical resection is reserved for residual or recurrent cancer in the anal canal after nonoperative therapy.
4. Alternately, salvage chemotherapy with fluorouracil and cisplatin combined with a radiation boost may avoid a permanent colostomy in patients with residual tumor following initial nonoperative therapy.[1]
5. Interstitial iridium-192 after external-beam radiation may convert some patients with residual disease into complete responders.[13]
Stage II anal cancer was formerly treated with abdominoperineal resection. Current sphincter-sparing therapies include wide local excision for small tumors of the perianal skin or anal margin, or definitive chemoradiation (fluorouracil and mitomycin) for cancers of the anal canal. Salvage chemotherapy (fluorouracil with cisplatin plus a radiation boost) may avoid permanent colostomy in patients with residual tumor following initial nonoperative therapy. Radical resection is reserved for patients with incomplete responses or recurrent disease. Therefore, continued surveillance with rectal examination every 3 months for the first 2 years and endoscopy/biopsy when indicated after completion of sphincter-preserving therapy is important.
Treatment options:
2. All other stage II cancers of the anal canal that involve the anal sphincter or are too large for complete local excision are treated with external beam radiation therapy plus chemotherapy.[2-8]
Chemotherapy with fluorouracil and mitomycin combined with primary radiation therapy appears to be more effective than radiation therapy alone.[9] The optimal dose of radiation with concurrent chemotherapy is under evaluation.[10-12]
Selected tumors are also suitable for interstitial irradiation.[3,13]
3. Radical resection is reserved for continued residual or recurrent cancer in the anal canal after nonoperative therapy.
4. Alternately, salvage chemotherapy with fluorouracil and cisplatin combined with a radiation boost may avoid a permanent colostomy in patients with residual tumor following initial nonoperative therapy.[8]
Stage IIIA anal cancer presents clinically as stage II in most instances and is determined to be IIIA by clinically evident perirectal nodal disease or adjacent organ involvement. Endorectal or endoanal ultrasound may aid in pretreatment staging.
Treatment options:
2. Postoperative radiation therapy.
The presence of inguinal nodes that are involved with metastatic disease (unilateral or bilateral) is a poor prognostic sign, although cure of this stage of disease is possible. Because of the poor prognosis associated with this stage, patients should be included in clinical trials whenever possible.
Treatment options:
Radiation therapy plus chemotherapy (as described for stage II) with surgical resection of residual disease at the primary site (local resection or abdominoperineal resection) and unilateral or bilateral superficial and deep inguinal node dissection for residual or recurrent tumor.
Patients in this stage should be considered candidates for clinical trials. There is no standard chemotherapy for patients with metastatic disease. Palliation of symptoms from the primary lesion is of major importance.
Treatment options:
2. Palliative irradiation.
3. Palliative combined chemotherapy and radiation therapy.
4. Clinical trials.
Local recurrences after treatment with either radiation therapy and chemotherapy or surgery as the primary treatment can be effectively controlled in a substantial number of patients by using the alternate treatment (surgical resection after radiation and vice versa).[1] Clinical trials are exploring the use of radiation therapy with chemotherapy and/or radiosensitizers to improve local control.
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Date Last Modified: 07/1999
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