National Cancer Institute®
Last Modified: February 1, 2002
1
UI - 11776626
AU - Wang L; Yu Z; Qian T
TI -
[Radiotherapy for early anal cancer: a report of 27 cases]
SO - Zhonghua Zhong Liu Za Zhi 1999 Nov;21(6):455-7
AD - Cancer Istitute (Hospital), Chinese Academy of Medical Sciences, Peking
Union Medical College, Beijing 100021.
OBJECTIVE: To evaluate the results of radiotherapy for early stage anal
cancer. METHODS: During 1960 through 1993, 27 patients with stage T1-2N0
anal cancer were treated by radiotherapy alone. Seven cases received
pelvic irradiation plus local field boost, 20 cases received local field
irradiation alone. Kaplan-Meier method was used in survival analysis.
RESULTS: The overall 5-year survival rate in this series of patients was
79.1%. Eighteen of the 27 cases had their anal functions preserved.
Local recurrence occurred in 7 cases and regional lymph node metastasis
in one case. Five of them were salvaged, two by surgery and three by
irradiation. CONCLUSION: Radiotherapy alone for early anal cancer is
effective. Anal function is preserved in about two-thirds of the
patients so treated. Local treatment failure can be salvaged by surgery
or radiotherapy.
2
UI - 11677963
AU - Indinnimeo M; Cicchini C; Stazi A; Limiti MR; Ghini C; Mingazzini PL;
TI -
Vecchione A
Prognostic impact of CD31 antigen expression in anal canal carcinoma.
SO - Hepatogastroenterology 2001 Sep-Oct;48(41):1355-8
AD - Department of Surgery Pietro Valdoni, Universita di Roma La Sapienza,
via del Policlinico, 155, 00161 Rome, Italy. marileda_indinni@yahoo.it
BACKGROUND/AIMS: CD31 is a platelet endothelial cell adhesion molecule.
Thus CD31 immunostaining of vascular endothelial cells can be used to
measure degree of angiogenesis. As angiogenesis is necessary for tumor
growth and metastasis, microvessels density could be a predictor of
prognosis. The purpose of this study was to examine the relationship
between CD31 value and standard pathologic parameters and prognosis of
anal canal carcinoma. METHODOLOGY: Twenty-four patients with anal canal
carcinoma were evaluated. Five-micron sections of formalin-fixed,
paraffin-embedded tissue were tested with monoclonal anti-CD31 antibody.
CD31 value is considered positive if more than 185 vessels/mm2 were
counted. Pearson's chi 2 test was employed to test for association
between CD31 value and clinicopathological variables. RESULTS: We found
no correlation between CD31 value and histologic type, lymph node
involvement, patients age and neoplastic relapse. Significant
correlation was found between CD31 score and depth of parietal invasion.
CONCLUSIONS: The relapse type could strengthen the hypothesis that
increased vascularity promotes neoplastic dissemination. As angiogenesis
could be used as prognostic indicator to determine patients who may be
at higher risk for relapse, our results warrant further confirmation.
Development of markers of angiogenic activity in anal canal carcinoma
must be an integral part of proper clinical trials.
3
UI - 11803628
AU - Kouas A; Hachicha I; Dahmane Y; Ben Ali A; Derbel F; Letaief R; Ben Hadj
TI -
Hamida R
[Anal metastasis of colonic adenocarcinoma?]
SO - Ann Chir 2001 Dec;126(10):1026-8
AD - Service de chirurgie generale et digestive, hopital Sahloul, Sousse,
Tunisie.
Two cases of sigmoid and anal adenocarcinoma are reported. The two
patients were treated by abdominoperineal resection of the rectum and
resection of the sigmoid colon. The relationship between colonic
adenocarcinoma and anal adenocarcinoma is not obvious but possible. The
various mechanisms of tumoral spread are discussed and the most frequent
mechanism seems to be cellular exfoliation.
4
UI - 11786758
AU - Tarantino D; Bernstein MA
TI -
Endoanal ultrasound in the staging and management of squamous-cell
carcinoma of the anal canal: potential implications of a new ultrasound
staging system.
SO - Dis Colon Rectum 2002 Jan;45(1):16-22
AD - Division of Colon and Rectal Surgery, St. Luke's/Roosevelt Hospital
Center, New York, New York, USA.
PURPOSE: This study was performed to determine whether endoanal
ultrasound could be used to accurately stage patients with squamous-cell
carcinoma of the anal canal and to determine the response of these
tumors to multimodality therapy. METHODS: Thirteen consecutive patients
with biopsy-proven squamous-cell carcinoma of the anal canal between
1996 and 1999 were included in the study. All patients underwent a
pretreatment staging endoanal ultrasound with a B&K 3535 ultrasound
machine using the 1850 rotating 360 degrees probe with a 10-MHz
transducer. Tumors were staged using our own modification of a 1984 TNM
staging system. For our study, a uT1 tumor was confined to the
submucosa; a uT2a lesion invaded only the internal anal sphincter; a
uT2b lesion penetrated into the external anal sphincter; a uT3 lesion
invaded through the sphincter complex into the perianal tissues; and a
uT4 lesion invaded adjacent structures. After the initial study,
patients decided on a course of treatment, either primary surgery or
chemoradiation. For patients choosing chemoradiation, a clinical
examination with biopsies and a repeat endoanal ultrasound was performed
after completion of therapy. Findings on physical examination and biopsy
results were compared with the follow-up endoanal ultrasound. For those
choosing surgery, the pathology specimen from the abdominoperineal
resection was reviewed and compared with the initial endoanal ultrasound
interpretation to determine the accuracy of endoanal ultrasound staging.
RESULTS: One patient died of complications from acquired
immunodeficiency syndrome before undergoing definitive treatment for his
anal cancer. Of the remaining 12 patients who comprised the study, the
endoscopic staging was as follows: 1 uT1, 5 uT2a, 3 uT2b, 2 uT3, and 1
uT4. Five of the 12 patients selected surgery as the primary treatment
modality for their disease. The other seven patients underwent a full
course of chemoradiation. In all five patients who had an
abdominoperineal resection, the surgical staging correlated with the
endoanal ultrasound staging (2 T2a tumors and 3 T2b tumors). In the
remaining seven patients, six to eight weeks after completion of
therapy, there was no evidence of residual tumor by clinical examination
and biopsies. In one of the seven patients, no abnormalities were
detected on endoanal ultrasound, and it was interpreted as normal with
no evidence of disease. In the remaining six patients, endoanal
ultrasound revealed abnormalities that were judged to represent
radiation-induced changes rather than residual disease. A repeat
endoanal ultrasound was done in these patients two to four months after
the biopsies. Complete resolution of the postradiation changes occurred
in all patients, and the scans were interpreted as showing no evidence
of disease. CONCLUSIONS: Endoanal ultrasound can accurately determine
the depth of penetration of squamous-cell carcinoma into the sphincter
complex and can be used to gauge accurately the response of these tumors
to chemoradiation therapy. Our newly proposed ultrasound staging system
may be more useful in choosing treatment options; future studies should
be aimed at using endoanal ultrasound in identifying early lesions that
may be amenable to less aggressive therapy as well as determining the
utility of ultrasound in the surveillance of patients after successful
treatment of their initial tumors.
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