Topotecan versus paclitaxel for the treatment of recurrent epithelial ovarian cancer - PubMed (original) (raw)
Clinical Trial
. 1997 Jun;15(6):2183-93.
doi: 10.1200/JCO.1997.15.6.2183.
M Gore, J Carmichael, A Gordon, J Malfetano, I Hudson, C Broom, C Scarabelli, N Davidson, M Spanczynski, G Bolis, H Malmström, R Coleman, S C Fields, J F Heron
Affiliations
- PMID: 9196130
- DOI: 10.1200/JCO.1997.15.6.2183
Clinical Trial
Topotecan versus paclitaxel for the treatment of recurrent epithelial ovarian cancer
W ten Bokkel Huinink et al. J Clin Oncol. 1997 Jun.
Abstract
Purpose: Topotecan and paclitaxel were evaluated in a randomized, multicenter study of patients with advanced epithelial ovarian carcinoma who had progressed during or after one platinum-based regimen.
Patients and methods: Patients received either topotecan (1.5 mg/m2) as a 30-minute infusion daily for 5 days every 21 days (n = 112) or paclitaxel (175 mg/m2) infused over 3 hours every 21 days (n = 114). Patients had bidimensionally measurable disease and were assessed for efficacy and toxicity.
Results: Response rate was 23 of 112 (20.5%) in topotecan-treated patients and 15 of 114 (13.2%) in paclitaxel-treated patients (P = .138). Disease stabilization for at least 8 weeks was noted in 30% of patients with topotecan and 33% of patients with paclitaxel. Median durations of response to topotecan and paclitaxel were 32 and 20 weeks, respectively (P = .222) and median times to progression were 23 and 14 weeks, respectively (P = .002). Median survival was 61 weeks for topotecan and 43 weeks for paclitaxel (P = .515). Response rates for topotecan and paclitaxel were 13.3% versus 6.7% (P = .303) in resistant patients (not responded to prior platinum-based therapy or progressed within 6 months of an initial response) and 28.8% versus 20.0% (P = .213) in sensitive patients (progressed > 6 months after response). Neutropenia was significantly more frequent on the topotecan arm 79% versus paclitaxel arm 23% (P < .01). It was short-lasting and noncumulative in both arms. Nonhematologic toxicities were generally mild (grades 1 to 2) for both agents.
Conclusion: Topotecan has efficacy at least equivalent to paclitaxel manifested by the higher response rate and significantly longer time to progression.
Comment in
- Treatment of recurrent ovarian cancer: increasing options--"recurrent" results.
Ozols RF. Ozols RF. J Clin Oncol. 1997 Jun;15(6):2177-80. doi: 10.1200/JCO.1997.15.6.2177. J Clin Oncol. 1997. PMID: 9196128 No abstract available.
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