Sequential mitoxantrone, daunorubicin, and cytosine arabinoside for patients with newly diagnosed acute myelocytic leukemia

被引:0
作者
Paciucci, PA
Cuttner, J
Gottlieb, A
Davis, RB
Martelo, O
Holland, JF
机构
[1] UPSTATE MED CTR SYRACUSE,SYRACUSE,NY
[2] UNIV CINCINNATI,COLL MED,CINCINNATI,OH
[3] HARVARD UNIV,SCH PUBL HLTH,CAMBRIDGE,MA 02138
关键词
mitoxantrone; cytosine arabinoside; AML;
D O I
10.1002/(SICI)1096-8652(199712)56:4<214::AID-AJH3>3.0.CO;2-#
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitoxantrone (M) is a synthetic aminoanthraquinone with anti-leukemic activity in patients with daunorubicin (D) resistant acute leukemia. The Cancer and Leukemia Group B (CALGB) has undertaken a limited access pilot study in which M, 12 mg/m(2), over 30 min, daily for 3 days, and cytosine arabinoside (Ara-C), 100 mg/m(2)/day by constant infusion for 7 days were used for the induction of newly diagnosed patients with AML. Responding patients were consolidated with daunorubicin, 45 mg/m(2)/day for 3 days, and 7 days of Ara-C. After a second consolidation identical to induction, no further therapy was given. Twenty-nine patients with a median age of 50 years (range 18-72) were entered in the study; 18 were males and 11 females. Twenty-four (83%) patients achieved CR, 1 patient achieved a PR, and 4 died in induction from leukemia-related causes. Two patients died in CR from consolidation-related neutropenic sepsis and two additional patients died in CR, Of 24 patients, 7 remain disease-free at a median follow-up interval of 8 years. The regimen is active and well tolerated. The duration of disease-free survival in responding patients is consistent with that seen in similar regimens using intensification chemotherapy without prolonged maintenance. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:214 / 218
页数:5
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