CISPLATIN, ADRIAMYCIN, ETOPOSIDE, MEGESTROL-ACETATE VERSUS MELPHALAN,5-FLUOROURACIL, MEDROXYPROGESTERONE ACETATE IN THE TREATMENT OF ENDOMETRIAL CARCINOMA
Tl. Cornelison et al., CISPLATIN, ADRIAMYCIN, ETOPOSIDE, MEGESTROL-ACETATE VERSUS MELPHALAN,5-FLUOROURACIL, MEDROXYPROGESTERONE ACETATE IN THE TREATMENT OF ENDOMETRIAL CARCINOMA, Gynecologic oncology, 59(2), 1995, pp. 243-248
Fifty consecutive patients with documented advanced or recurrent endom
etrial carcinoma from 1978 through 1985 were prospectively treated wit
h melphalan, 5-fluorouracil, medroxyprogesterone acetate (MFP) as firs
t-line chemotherapy. From 1987 through 1993, 50 consecutive patients w
ith documented advanced or recurrent endometrial carcinoma were prospe
ctively treated with cisplatin, Adriamycin, etoposide, megestrol aceta
te (PAV-M) as first-line chemotherapy. Response rates for MFP versus P
AV-M, 2- and 5-year survival, median survival, 2- and 5-year progressi
on-free survival, and median progression-free survival were not statis
tically different. However, there was a significant improvement favori
ng PAV-M in 2-year (45 versus 14%), 5-year (30 versus 5%), and median
survival (22.3 versus 8.7 months) (P = 0.008) compared to MFP in patie
nts with primary advanced endometrial adenocarcinoma. Moreover, there
was a significant improvement in 2- and 5-year and median survival (55
and 15% and 26.7 months) for PAV-M compared to MFP (7 and 0% and 7.3
months) (P = 0.002) for the more aggressive other adenocarcinomas (ade
nosquamous, clear cell, papillary serous, undifferentiated) compared t
o the more common endometrioid adenocarcinoma. The current data sugges
t that cisplatin- and adriamycin-based chemotherapy results in some lo
ng-term survival benefit for patients with primary advanced endometria
l adenocarcinoma and the more aggressive nonendometrioid adenocarcinom
a histologies. (C) 1995 Academic Press, Inc.