HOMOHARRINGTONINE THERAPY INDUCES RESPONSES IN PATIENTS WITH CHRONIC MYELOGENOUS LEUKEMIA IN LATE CHRONIC PHASE

被引:140
作者
OBRIEN, S
KANTARJIAN, H
KEATING, M
BERAN, M
KOLLER, C
ROBERTSON, LE
HESTER, J
RIOS, M
ANDREEFF, M
TALPAZ, M
机构
关键词
D O I
10.1182/blood.V86.9.3322.bloodjournal8693322
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Homoharringtonine (HHT) is a plant alkaloid with potent myelosuppressive activity and little toxicity when used in a continuous infusion schedule, The antileukemic efficacy of HHT has been shown in acute myeloid leukemia, but has not been investigated in chronic myelogenous leukemia (CML), seventy-one patients with Philadelphia chromosome-positive (Ph(+)) CML in late chronic phase (time from diagnosis to therapy longer than 12 months) were treated with a continuous infusion of HHT at a daily dose of 2.5 mg/m(2) for 14 days for remission induction and for 7 days every month for maintenance, The median number of courses given was 6 (range, 1 to 35) and 21 patients (30%) continue on treatment. Forty-two of 58 patients (72%) evaluable for hematologic response achieved a complete hematologic remission, and 9 (16%) had a partial hematologic remission. Twenty-two of 71 patients (31%) developed a cytogenetic response; it was major (Ph(+) cells less than 35%) in 11 (15%) and complete (Ph(+) cells 0%) in 5 (7%). Significant myelosuppression occurred in 39% of induction courses and 9% of maintenance courses. Fever or documented infection was present in 26% of induction courses and in only 8% of maintenance courses. Nonmyelosuppressive toxicity was minimal, Homoharringtonine produced hematologic remissions in the majority of patients with advanced chronic-phase CML. Cytogenetic response occurred in some patients without an association with myelosuppression, and these responses may be prolonged. Future studies investigating homoharringtonine in combination with other active agents in CML, such as interferon, are warranted. (C) 1995 by The American Society of Hematology.
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页码:3322 / 3326
页数:5
相关论文
共 20 条
[1]  
[Anonymous], 1977, CHIN MED J, V3, P319
[2]  
CARELLA AM, 1993, BONE MARROW TRANSPL, V12, P267
[3]  
Chinese People's Liberation Army (PLA), 1978, CHIN MED J, V3, P163
[4]   INDUCTION OF CHRONIC MYELOGENOUS LEUKEMIA IN MICE BY THE P210BCR/ABL GENE OF THE PHILADELPHIA-CHROMOSOME [J].
DALEY, GQ ;
VANETTEN, RA ;
BALTIMORE, D .
SCIENCE, 1990, 247 (4944) :824-830
[5]  
KANTARJIAN HM, 1989, CANCER, V63, P813, DOI 10.1002/1097-0142(19890301)63:5<813::AID-CNCR2820630502>3.0.CO
[6]  
2-V
[7]  
KANTARJIAN HM, 1991, CANCER-AM CANCER SOC, V68, P1201, DOI 10.1002/1097-0142(19910915)68:6<1201::AID-CNCR2820680604>3.0.CO
[8]  
2-1
[9]   PROLONGED SURVIVAL IN CHRONIC MYELOGENOUS LEUKEMIA AFTER CYTOGENETIC RESPONSE TO INTERFERON-ALPHA THERAPY [J].
KANTARJIAN, HM ;
SMITH, TL ;
OBRIEN, S ;
BERAN, M ;
PIERCE, S ;
TALPAZ, M ;
ROBERTSON, L ;
KOLLER, C ;
ESTEY, E ;
KEATING, MJ .
ANNALS OF INTERNAL MEDICINE, 1995, 122 (04) :254-261
[10]   TREATMENT OF ADVANCED STAGES OF PHILADELPHIA CHROMOSOME-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA WITH INTERFERON-ALPHA AND LOW-DOSE CYTARABINE [J].
KANTARJIAN, HM ;
KEATING, MJ ;
ESTEY, EH ;
OBRIEN, S ;
PIERCE, S ;
BERAN, M ;
KOLLER, C ;
FELDMAN, E ;
TALPAZ, M .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (05) :772-778