Treatment of relapsed chronic lymphocytic leukemia by 72-hour continuous infusion or 1-hour bolus infusion of flavopiridol: Results from cancer and leukemia group B study 19805

被引:99
作者
Byrd, JC
Peterson, BL
Gabrilove, J
Odenike, OM
Grever, MR
Rai, K
Larson, RA
机构
[1] Ohio State Univ, Div Hematol Oncol, Dept Med, Columbus, OH 43210 USA
[2] Duke Univ, Med Ctr, Canc & Leukemia Grp B, Ctr Stat, Durham, NC USA
[3] Mt Sinai Hosp, Div Neuroplast Dis, New York, NY 10029 USA
[4] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[5] Long Isl Jewish Med Ctr, Div Hematol, New Hyde Pk, NY 11042 USA
[6] Long Isl Jewish Med Ctr, Div Oncol, New Hyde Pk, NY 11042 USA
关键词
D O I
10.1158/1078-0432.CCR-04-2276
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Flavopiridol has in vitro activity in chronic lymphocytic leukemia (CLL) and promotes apoptosis independent of p53 function or prior fludarabine exposure. We sought to determine if flavopiridol has activity in previously treated CLL using two schedules of administration. Patients and Methods: Patients with previously treated CLL were enrolled in two sequentially done phase II studies. Patients in the first trial received flavopiridol (50 mg/m(2)/d) as a continuous infusion (CI) for 72 hours every 2 weeks. Patients in the second trial received flavopiridol 50 mg/m(2) as a 1-hour bolus (IVB) daily for 3 days repeated every 3 weeks. Patients received up to 12 (Cl cohort) or 8 (IVB cohort) cycles of therapy. Results: Fifteen patients were enrolled in the 72-hour Cl phase II trial; 6 (40%) had intermediate-risk (Rai stage I or II) and 9 (60%) had high-risk (Rai stage III and IV) stages. No responses were noted in this group; 27% had stable disease and 73% had progressive disease. Thirty-six patients were enrolled in the second IVB trial, with 13 (36%) having intermediate and 23 (64%) having high-risk disease. Four patients (11%) had partial responses, 19 (53%) had stable disease, and 13 (36%) had progressive disease. The progression-free survival for responders in the IVB trial was 3, 3, 9, and 19 months. The median progression-free survival was 2 months [95% confidence interval (95% CI), 1.8-3.8] for patients in the Cl trial and 3 months (95% Cl, 2.5-7.4) for the IVB trial. The median overall survival was 27 months (95% Cl, 20-42) for the CI trial and 24 months (95% Cl, 18-31) for the IVB trial. Toxicity was manageable and included mainly myelosuppression, infections, diarrhea, and fatigue. Conclusions: Flavopiridol has modest, schedule-dependent clinical activity in relapsed CLL and warrants future investigation utilizing alternative schedules of administration.
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页码:4176 / 4181
页数:6
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