A phase II study of carboplatin and cisplatin in advanced ovarian cancer

E. Segelov, R. Stuart-Harris, D. Bell, M. Tattersall, J. Hutton-Potts, M. Friedlander

Research output: Contribution to journalArticleResearchpeer-review

4 Citations (Scopus)

Abstract

In view of the single agent activity of both cisplatin and carboplatin in epithelial ovarian cancer, and their different toxicity profiles, we carried out a phase II study of low dose cisplatin (50 mg/m2) in combination with moderate dose carboplatin (300 mg/m2) in patients with advanced ovarian cancer. Fourteen patients, all of whom had bulky disease and over half of whom had Stage IV disease, were eligible for assessment of response and toxicity. An overall response rate of 71% was demonstrated (57% complete response, 14% partial response), which is at least equivalent to other regimens used in first line treatment of ovarian cancer. Toxicities encountered were nausea/vomiting and myelosuppression, however no serious renal neuro or ototoxicity was observed and the regimen does not cause significant alopecia. This combination may be a practical alternative to regimens which use high dose cisplatin to achieve similar efficacy.

Original languageEnglish
Pages (from-to)277-282
Number of pages6
JournalEuropean Journal of Gynaecological Oncology
Volume15
Issue number4
Publication statusPublished - 1 Jan 1994
Externally publishedYes

Cite this