CPT-11 - A NEW DERIVATIVE OF CAMPTOTHECIN FOR THE TREATMENT OF REFRACTORY OR RELAPSED SMALL-CELL LUNG-CANCER

被引:412
作者
MASUDA, N
FUKUOKA, M
KUSUNOKI, Y
MATSUI, K
TAKIFUJI, N
KUDOH, S
NEGORO, S
NISHIOKA, M
NAKAGAWA, K
TAKADA, M
机构
[1] OSAKA PREFECTURAL HABIKINO HOSP,DEPT INTERNAL MED,3-7-1 HABIKINO,HABIKINO,OSAKA 583,JAPAN
[2] OSAKA PREFECTURAL HABIKINO HOSP,DEPT RADIOL,HABIKINO,OSAKA,JAPAN
关键词
D O I
10.1200/JCO.1992.10.8.1225
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the activity of CPT-11, which is a new derivative of camptothecin, against refractory or relapsed small-cell lung cancer (SCLC). Patients and Methods: Sixteen patients with refractory or relapsed SCLC were entered onto a prospective, nonrandomized, single-institution phase II trial. All 16 patients had been pretreated heavily with some form of cisplatin-based combination chemotherapy. Five patients had received previous chemotherapy with cisplatin, vincristine, doxorubicin, and etoposide (CODE) as an induction therapy. Six patients had been treated with concurrent cisplatin and etoposide plus chest x-ray. The median time off chemotherapy was 7.3 months (range, 1.9 to 15.1 months). Patients were treated with a CPT-11 starting dose of 100 mg/m2 body surface given as a 90-minute intravenous (IV) infusion every week with subsequent doses based on toxicity. Fifteen patients were assessable for toxicity, response, and survival. Results: Seven patients (47%; 95% confidence limits for an overall response rate, 21.4% to 71.9%) responded to CPT-11 with a median duration of response of 58 days. The major toxicities were myelosuppression (predominantly leukopenia), diarrhea, and pulmonary toxicity. Conclusion: CPT-11 is an active agent against refractory or relapsed SCLC and deserves to be studied more closely as both a single agent and in combination with other drugs to treat patients with SCLC. © 1992 by American Society of Clinical Oncology.
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页码:1225 / 1229
页数:5
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