VIENNA--For women with advanced epithelial ovarian cancer who fail one platinum-based regimen, topotecan (Hycamtin) may represent a promising alternative to paclitaxel (Taxol), reported W. W. ten Bokkel Huinink, MD, of the Netherlands Cancer Institute.
VIENNA--For women with advanced epithelial ovarian cancer who fail oneplatinum-based regimen, topotecan (Hycamtin) may represent a promisingalternative to paclitaxel (Taxol), reported W. W. ten Bokkel Huinink, MD,of the Netherlands Cancer Institute.
He spoke at the 21st Congress of the European Society for Medical Oncology(ESMO) on behalf of the International Topotecan Study Group.
Dr. ten Bokkel Huinink and his co-investigators in Europe, the UnitedStates, and Canada randomized study enrollees to treatment every 3 weekswith either topotecan, 1.5 mg/m2 as a 30-minute infusion dailyfor 5 days, or paclitaxel, 175 mg/m2 as a 3-hour infusion. Patientsreceived an average of three to five courses.
The topoisomerase I inhibitor achieved a response rate of 21% with aduration of 26 weeks, compared with 14% and 22 weeks for paclitaxel. Thesedifferences failed to reach statistical significance in this 226-patientstudy. Nonetheless, Dr. ten Bokkel Huinink said, topotecan stretched thetime to progression to 19 weeks vs 15 weeks with paclitaxel (P less than.05), and prolonged overall survival to 63 weeks vs 53 weeks with paclitaxel.
The trial also revealed a 13% response rate among women who failed torespond to paclitaxel and were switched to topote-can, and an 8% responserate in topotecan failures after crossover to paclitaxel.
"I'm one of the few investigators to have experience with the combinationof cisplatin and paclitaxel, and topotecan is the only drug I know to havesome activity in women already pretreated with cisplatin and paclitaxel,"Dr. ten Bokkel Huinink commented.
An apparent downside of topotecan therapy was a higher percentage oftreatment courses complicated by grade 3 or 4 neutropenia, thrombocytopenia,and anemia. However, the Topotecan Study Group characterized these hematologictoxicities as "reversible, noncumulative, and manageable."
An ongoing US-European trial involving about 400 patients is currentlyweighing the comparative efficacy of cisplatin-topotecan and cisplatin-paclitaxelas first-line regimens for ovarian cancer.