A multi-center phase II study of weekly topotecan as second-line therapy for small cell lung cancer

被引:27
作者
Shah, Chirag
Ready, Neal
Perry, Michel
Kirshner, Jeffrey
Gajra, Ajeet
Neuman, Nancy
Garziano, Stephen
机构
[1] SUNY Upstate Med Univ, Reg Oncol Ctr, Dept Med, Syracuse, NY 13210 USA
[2] Duke Univ, Med Ctr, Durham, NC 27710 USA
[3] Univ Missouri, Ellis Fischel Canc Ctr, Dept Med, Columbia, MO 65203 USA
[4] Hematol Oncol Associates Cent New York PC, E Syracuse, NY 13057 USA
关键词
small cell lung cancer; topotecan; weekly schedule; sensitive relapse; CHEMOTHERAPY; CISPLATIN; ETOPOSIDE; CYCLOPHOSPHAMIDE; VINCRISTINE; DOXORUBICIN; PACLITAXEL; CARCINOMA; TRIAL;
D O I
10.1016/j.lungcan.2007.02.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the response rate, toxicity, failure free and overall. survival of weekly topotecan in patients with relapsed small. cell lung cancer who received one prior platinum based chemotherapy. Patients and methods: Twenty two patients with relapsed disease after response to one prior chemotherapy with or without radiotherapy and patients with relapse more than 90 days after their last therapy received topotecan 4 mg/m(2) intravenous over 30 min on days 1,8,15; every 4 weeks (3 weeks on and 1 weeks off). Chemotherapy was given until disease progression or unacceptable toxicity. Results: Of 22 patients, none of the patients responded to weekly topotecan therapy. Four patients had stable disease. After a median follow up of 1 year, median time to progression was 6 weeks and median survival was 5 months. The common toxicities associated with this regimen were anemia, thrombocytopenia, fatigue, GI side effects and alopecia. Conclusion: Weekly topotecan was well tolerated but ineffective in this trial. Although commonly used, weekly regimen of topotecan should be used with caution in relapsed SCLC. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:84 / 88
页数:5
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