METAANALYSIS OF CHEMOTHERAPY REGIMENS FOR OVARIAN-CARCINOMA - A REASSESSMENT OF CISPLATIN, CYCLOPHOSPHAMIDE AND DOXORUBICIN VERSUS CISPLATIN AND CYCLOPHOSPHAMIDE
Rj. West et Sf. Zweig, METAANALYSIS OF CHEMOTHERAPY REGIMENS FOR OVARIAN-CARCINOMA - A REASSESSMENT OF CISPLATIN, CYCLOPHOSPHAMIDE AND DOXORUBICIN VERSUS CISPLATIN AND CYCLOPHOSPHAMIDE, European journal of gynaecological oncology, 18(5), 1997, pp. 343-348
Objective: To compare three year survival, median survival and improve
d longevity with the addition of doxorubicin to a chemotherapy regimen
of cisplatin and cyclophospamide used in the treatment of ovarian can
cer and to integrate this with a previous meta-analysis that compared
three year survival. Methods: Twenty-three studies that evaluated eith
er the control or test arms were combined for meta-analysis. Five stud
ies were randomized with both arms. Inclusion criteria consisted of me
dian survival data, three year survival data, no previous chemotherapy
or radiation and adequate follow-up. The data were analyzed with a tw
o-tailed t test, a fixed effects odds ratio, a random effects odds rat
io, logistic repression modelling for three year survival and standard
regression modelling for median survival. Results: A statistically si
gnificant improvement in three year survival was demonstrated with the
fixed effects odds ratio analysis combining the five prospective rand
omized studies and with logistic regression model of all the studies.
Random effects odds ratio and the two-tailed t test failed to show sta
tistical significance. Standard regression modelling demonstrated stat
istically significant improvement in median survival for a doxorubicin
dose intensity of 40 mg/m(2) and near significance for a doxorubicin
dose intensity of 50 mg/m(2). Median survival was improved by 1.91 mon
ths with the addition of doxorubicin to the cisplatin/cyclophosphamide
regimen. Conclusion: Although there appears to be statistically signi
ficant improvement in three year survival and median survival with the
addition of doxorubicin to the cisplatin/cyclophoshamide regimen for
ovarian cancer, the actual improvement in median survival is less than
two months and therefore, the added toxicity of doxorubicin may not b
e warranted.