INTERFERON-ALPHA PRODUCES SUSTAINED CYTOGENETIC RESPONSES IN CHRONIC MYELOGENOUS LEUKEMIA - PHILADELPHIA CHROMOSOME-POSITIVE PATIENTS

被引:423
作者
TALPAZ, M
KANTARJIAN, H
KURZROCK, R
TRUJILLO, JM
GUTTERMAN, JU
机构
[1] University of Texas, M.D. Anderson Cancer Center, Houston, TX
[2] Dept. Clin. Immunol. and Biol. Ther., Box 41, Univ. Texas M.D. Anderson Cancer C., Houston, TX 77030
[3] University of Texas, M.D. Anderson Cancer Center, Houston, TX 77030
关键词
D O I
10.7326/0003-4819-114-7-532
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To evaluate the frequency and the course of complete cytogenetic responses in interferon-alpha (IFN-alpha)-treated patients with chronic myelogenous leukemia. Design: Two prospective trials in consecutive patients. Setting: A major tertiary cancer center. Patients: Ninety-six consecutive patients with chronic myelogenous leukemia with disease duration of less than 1 year. Intervention: Patients received partially pure IFN-alpha intramuscularly, from 3 to 9 million U/d (51 patients) or recombinant IFN-alpha-2a (Roferon, Hoffmann-LaRoche, Inc., Nutley, New Jersey), 5 million U/m2 body surface area daily (45 patients). Measurements: Hematologic and cytogenetic tests were administered. Main Results: Seventy of the patients (73%) achieved hematologic remission (95% CI, 63% to 81%), and 18 (19%) had complete suppression of the Philadelphia chromosome on at least one cytogenetic test. A complete cytogenetic response was induced in 7 of 51 or 14% (CI, 6% to 26%) of the patients treated with the partially pure IFN-alpha and in 11 of 45 or 24% (CI, 13% to 40%) of the patients treated with recombinant IFN-alpha-2a. The difference in complete cytogenetic response between the two groups was 10.7% (CI, -5% to 26%; P > 0.2). Eleven patients had durable, ongoing, complete cytogenetic responses from 6 to more than 45 months (median, more than 30 months). Conclusion: This study was the first to show sustained, complete cytogenetic responses in a subset of patients with chronic myelogenous leukemia treated with single-agent therapy. The nature of this remission, that is, whether it depends on continuous therapy, requires further study.
引用
收藏
页码:532 / 538
页数:7
相关论文
共 26 条
[1]  
ARTHUR CK, 1988, BLOOD, V71, P1179
[2]  
CHAMPLIN RE, 1985, BLOOD, V65, P1039
[3]   LONG-TERM MARROW CULTURE REVEALS CHROMOSOMALLY NORMAL HEMATOPOIETIC PROGENITOR CELLS IN PATIENTS WITH PHILADELPHIA CHROMOSOME-POSITIVE CHRONIC MYELOGENOUS LEUKEMIA [J].
COULOMBEL, L ;
KALOUSEK, DK ;
EAVES, CJ ;
GUPTA, CM ;
EAVES, AC .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 308 (25) :1493-1498
[4]  
CUNNINGHAM I, 1979, BLOOD, V53, P375
[5]  
DUBE ID, 1984, BLOOD, V63, P1172
[6]   CHANGES IN THE BONE-MARROW OF CANCER-PATIENTS TREATED WITH RECOMBINANT INTERFERON ALPHA-2 [J].
ERNSTOFF, MS ;
KIRKWOOD, JM .
AMERICAN JOURNAL OF MEDICINE, 1984, 76 (04) :593-596
[7]   LEUKOCYTE INTERFERON-INDUCED TUMOR-REGRESSION IN HUMAN METASTATIC BREAST-CANCER, MULTIPLE-MYELOMA, AND MALIGNANT-LYMPHOMA [J].
GUTTERMAN, JU ;
BLUMENSCHEIN, GR ;
ALEXANIAN, R ;
YAP, HY ;
BUZDAR, AU ;
CABANILLAS, F ;
HORTOBAGYI, GN ;
HERSH, EM ;
RASMUSSEN, SL ;
HARMON, M ;
KRAMER, M ;
PESTKA, S .
ANNALS OF INTERNAL MEDICINE, 1980, 93 (03) :399-406
[8]   INTENSIVE COMBINATION CHEMOTHERAPY (ROAP-10) AND SPLENECTOMY IN THE MANAGEMENT OF CHRONIC MYELOGENOUS LEUKEMIA [J].
KANTARJIAN, HM ;
VELLEKOOP, L ;
MCCREDIE, KB ;
KEATING, MJ ;
HESTER, J ;
SMITH, T ;
BARLOGIE, B ;
TRUJILLO, J ;
FREIREICH, EJ .
JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (02) :192-200
[9]  
KANTARJIAN HM, 1985, BLOOD, V66, P1326
[10]   CHRONIC MYELOGENOUS LEUKEMIA - NEW CONCEPTS .2. [J].
KOEFFLER, HP ;
GOLDE, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (21) :1269-1274