Parallel phase I studies of daunorubicin given with cytarabine and etoposide with or without the multidrug resistance modulator PSC-833 in previously untreated patients 60 years of age or older with acute myeloid leukemia: Results of cancer and leukemia group B study 9420

被引:72
作者
Lee, EJ
George, SL
Caligiuri, M
Szatrowski, TP
Powell, BL
Lemke, S
Dodge, RK
Smith, R
Baer, M
Schiffer, CA
机构
[1] Univ Maryland, Sch Med, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Duke Univ, Ctr Comprehens Canc, Durham, NC USA
[3] Wake Forest Univ, Ctr Comprehens Canc, Sch Med, Winston Salem, NC 27109 USA
[4] Ohio State Univ, Sch Med, Columbus, OH 43210 USA
[5] Cornell Univ, Sch Med, New York, NY 10021 USA
[6] SUNY Hlth Sci Ctr, Syracuse, NY 13210 USA
[7] Roswell Pk Canc Inst, Buffalo, NY USA
[8] Ann Karmanos Canc Inst, Detroit, MI USA
[9] Wayne State Univ, Sch Med, Detroit, MI USA
[10] Canc & Leukemia Grp B, Chicago, IL USA
关键词
D O I
10.1200/JCO.1999.17.9.2831
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The Cancer and Leukemia Group B conducted parallel phase I trials of cytarabine, daunorubicin, and etoposide (ADE) with or without PSC-833 (P), a modulator of p-glycoprotein-mediated multidrug resistance, Patients and Methods: One hundred ten newly diagnosed patients greater than or equal to 60 years of age with de navo acute myeloid leukemia (AML) were treated. All patients received cytarabine by continuous infusion for 7 days at 100 mg/m(2)/d. The starting dose of daunorubicin was 30 mg/m(2)/d for 3 days. Etoposide was administered at a dose of 100 mg/m2/d for 3 days, except in the last cohort administered ADEP, who received 60 mg/m(2). PSC-833 was given intravenously with a loading dose of 1.5 mg/kg over 2 hours and a simultaneous continuous infusion of 10 mg/kg/d continued until 24 hours after the last dose of daunorubicin or etoposide, Results: There was no toxicity attributed to the PSC-833, Dose-limiting toxicity was primarily gastrointestinal (diarrhea, mucositis in the ADEP group). The estimated maximum-tolerated doses, calculated using a logistic regression model, were daunorubicin 40 mg/m2/d for 3 days with etoposide 60 mg/m(2) for 3 days in the ADEP group and daunorubicin 60 mg/m(2)/d for 3 days and etoposide 100 mg/m(2)/d for 3 days in the ADE group, Twenty-one (48%) of 44 patients achieved complete remission with ADE, compared with 29 (44%) of 66 patients treated with ADEP. Conclusion: It is necessary to decrease the doses of daunorubicin and etoposide when they are administered with PSC-833, presumably because of the effect of the modulator on the pharmacokinetics of these agents. A phase III trial comparing the regimens derived from this phase I trial has recently begun. (C) 1999 by American Society of Clinical Oncology.
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页码:2831 / 2839
页数:9
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