TREATMENT OF ADVANCED STAGES OF PHILADELPHIA CHROMOSOME-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA WITH INTERFERON-ALPHA AND LOW-DOSE CYTARABINE

被引:111
作者
KANTARJIAN, HM
KEATING, MJ
ESTEY, EH
OBRIEN, S
PIERCE, S
BERAN, M
KOLLER, C
FELDMAN, E
TALPAZ, M
机构
[1] MD ANDERSON CANC CTR, DEPT HEMATOL, HOUSTON, TX USA
[2] MD ANDERSON CANC CTR, DEPT CLIN IMMUNOL, HOUSTON, TX USA
[3] MD ANDERSON CANC CTR, DEPT BIOL THERAPY, HOUSTON, TX USA
关键词
D O I
10.1200/JCO.1992.10.5.772
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the efficacy of interferon-α (IFN-A) and low-dose cytarabine (ara-C) combination chemotherapy in patients with chronic myelogenous leukemia (CML). Patients and Methods: Sixty patients with advanced phases of Philadelphia chromosome (Ph)-positive CML received combination therapy with IFN-A 5 × 106 U/m2 daily, and low-dose ara-C 15 mg/m2 daily for 2 weeks every 4 weeks until remission, then for 1 week every month as maintenance. Forty patients were in late chronicphase CML, and 20 were in accelerated-phase CML (16 with clonal evolution only, four with other criteria). Their outcome was compared with 58 patients (39 late chronicphase CML and 19 accelerated-phase CML) who had been previously treated with IFN-A alone in the same dose schedule. Results: In late chronic-phase CML, patients receiving IFN-A plus ara-C had a better complete hematologic response (CHR) rate compared with those treated with IFN-A alone (55% v 28%; P = .02), a trend for better Ph suppression (15% v 5%; P = .13), and a longer survival (3-year survival rate 75% v 48%; P < .01). These differences do not seem to be caused by imbalances in prognostic factors between the two treatment groups. In accelerated-phase CML, the addition of ara-C to IFN-A did not improve the response rate of treated patients, and the difference in survival was accounted for by different patient characteristics. Suppression of clonal evolution was observed in five patients (25%). Patients with clonal evolution as the only criterion for disease acceleration had a longer survival than those with other or additional accelerated-phase criteria (3-year survival rate 67% v 22%; P < .01). Conclusion: The results with the combination of IFN-A plus ara-C in late chronic-phase CML are encouraging, and suggest the need for its evaluation in early chronicphase CML. © 1992 by American Society of Clinical Oncology.
引用
收藏
页码:772 / 778
页数:7
相关论文
共 19 条
[1]   CHRONIC GRANULOCYTIC LEUKEMIA [J].
CANELLOS, GP .
MEDICAL CLINICS OF NORTH AMERICA, 1976, 60 (05) :1001-1018
[2]   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
[3]   BONE-MARROW TRANSPLANTATION FOR PATIENTS WITH CHRONIC MYELOID-LEUKEMIA [J].
GOLDMAN, JM ;
APPERLEY, JF ;
JONES, L ;
MARCUS, R ;
GOOLDEN, AWG ;
BATCHELOR, R ;
HALE, G ;
WALDMANN, H ;
REID, CD ;
HOWS, J ;
GORDONSMITH, E ;
CATOVSKY, D ;
GALTON, DAG .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (04) :202-207
[4]  
IMANISHI J, 1984, JPN J CANC CHEMOTHER, V11, P53
[5]  
KANTARJIAN H M, 1988, Hematologic Pathology, V2, P91
[6]  
KANTARJIAN HM, 1988, CANCER, V61, P1441, DOI 10.1002/1097-0142(19880401)61:7<1441::AID-CNCR2820610727>3.0.CO
[7]  
2-C
[8]  
KANTARJIAN HM, 1985, BLOOD, V66, P1326
[9]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[10]  
MANTEL NATHAN, 1966, CANCERCHEMOTHERAP REP, V50, P163