DOXORUBICIN-MELPHALAN WITH AND WITHOUT CISPLATIN IN ADVANCED OVARIAN-CANCER - 10-YEAR SURVIVAL RESULTS FROM A PROSPECTIVE RANDOMIZED STUDY BY THE SWEDISH COOPERATIVE OVARIAN-CANCER STUDY-GROUP
C. Trope et al., DOXORUBICIN-MELPHALAN WITH AND WITHOUT CISPLATIN IN ADVANCED OVARIAN-CANCER - 10-YEAR SURVIVAL RESULTS FROM A PROSPECTIVE RANDOMIZED STUDY BY THE SWEDISH COOPERATIVE OVARIAN-CANCER STUDY-GROUP, Acta oncologica, 35, 1996, pp. 109-118
In a controlled prospective randomized study the regimen doxorubicin (
A) 40 mg/m(2) + melphalan (M) 0.4 mg/kg was compared with A+M+cisplati
n (C) 50 mg/m(2) given every four weeks in advanced ovarian cancer, FI
GO stage III or IV and with serous or anaplastic histology. From 1981
to 1983, 300 patients entered the study and 295 patients were evaluabl
e for response, toxicity and long-term survival. All patients were fol
lowed for at least 10 years. The majority of patients had large residu
al tumours >2 cm. Patients treated with MAC had a higher response rate
compared with patients treated with MA (76% vs, 50%, p<0.01) and trea
tment with MAC resulted in significantly more pathological complete re
sponders than MA. There was a significant difference in median duratio
n of response (19 months vs. 13 months, p<0.006) and in median surviva
l time (26 months vs. 19 months, p=0.05). After 5- and 10 years a sign
ificant difference in progression-free and overall survival was found.
The independent prognostic factors in this study were residual tumour
after primary surgery, treatment with MAC, tumour grade, ascites, and
stage, objective and subjective side effects were significantly worse
with MAC, although tolerable. In conclusion, this study shows that in
corporating C into MA improves the duration of progression-free surviv
al and overall survival in women with incompletely resected Stage III
or Stage IV ovarian epithelial cancer. A 5- and 10-year survival of 25
% and 18%, respectively, is impressive.