Background and Objectives: Colorectal sarcomas (CRS) are rare and thei
r treatment remains controversial, especially fur those located in the
rectum. The aim of this paper is to evaluate our experience, with spe
cial emphasis on the failure pattern after surgical therapy alone or c
ombined with postoperative radiotherapy. Materials and Methods: The me
dical records and histological slides of 13 CRS patients treated betwe
en 1986 and 1996 were reviewed retrospectively. Results: The patients
included eight males and five females, with a median age of 54 years;
nine of their primary tumors were located in the rectum, and four in t
he colon. The histologies were leiomyosarcoma in nine cases and malign
ant fibrous histiocytoma in four cases. Surgical treatment consisted o
f anatomical colectomy (four): local excision (three): abdominoperinea
l resection (APR)(two); low anterior resection (LAR)(two): LAR en bloc
with the prostate lone). and total pelvic exenteration lone). One ope
rative death occurred. The median size of the tumors was 8 cm (range.
5-40). The turners were graded as low, three, and high, ten. The media
n follow-up was 24 months. Eight patients in the overall group develop
ed recurrences as follows: local. three; local and distant, three, and
distant, two. Five out of nine patients with rectal sar coma received
adjuvant postoperative radiotherapy (PRT). Local recurrence occurred
in 20% (1/5) of those who received PRT, and in 100% (3/3) of those who
did nor. The overall 5-year survival was 40%, and the 5-year survival
for patients with low-grade tumors was 66%, as compared with 22% for
those with high-grade tumors. Conclusions: The patterns of failure in
CRS are combined in both local and distant sites. However, our results
suggest that in rectal sarcoma, the use of surgery + PRT may reduce t
he local recurrence rate; in selected patients, it may allow for anal
sphincter preservation. (C) 1998 Wiley-Liss, Inc.