B. Jereczek et al., PRIMARY-CANCER OF THE FALLOPIAN-TUBE - REPORT OF 26 PATIENTS, Acta obstetricia et gynecologica Scandinavica, 75(3), 1996, pp. 281-286
Background. Due to rarity of fallopian tube cancer most series on this
tumor are small and many problems have remained unsolved. The aim of
this report is to review our experience with this neoplasm and to comp
are it with previously published data. Methods. Retrospective study of
26 patients with fallopian tube cancer treated in one institution bet
ween 1974 and 1994. All patients underwent primary surgical treatment
and 18 received adjuvant therapy including pelvic irradiation in 14 ca
ses and chemotherapy in four. Results. Relapse occurred in 18 out of 2
5 followed up patients. Upper abdominal component of relapse was encou
ntered in 12 patients (67%), pelvic component - in eight (44%) and ext
raperitoneal component - in six (33%). Pelvic relapse occurred in two
out of 13 followed up patients treated with postoperative irradiation
and in six out of 12 who did not receive postoperative radiotherapy Su
rvival ranged from 6 to 218+months (median 23 months). Five-year actua
l survival was 33%. There were no 2-year survivors in patients present
ing with stage II-IV disease. No correlation was found between tumor g
rade and survival. Conclusions. Fallopian tube cancer is a treatable d
isease but cure can be only achieved in patients with early tumor. Pos
toperative radiotherapy may result in better local control but does no
t preclude extrapelvic dissemination, therefore adjuvant chemotherapy
should be considered in high risk patients. Registration of all new ca
ses as well as prospective multicenter studies are warranted to establ
ish optimal management. (C) Acta Obstet Gynecol Scand 1996