USE OF GRANULOCYTE-COLONY-STIMULATING FACTOR BEFORE, DURING, AND AFTER FLUDARABINE PLUS CYTARABINE INDUCTION THERAPY OF NEWLY-DIAGNOSED ACUTE MYELOGENOUS LEUKEMIA OR MYELODYSPLASTIC SYNDROMES - COMPARISON WITH FLUDARABINE PLUS CYTARABINE WITHOUT GRANULOCYTE-COLONY-STIMULATING FACTOR

被引:286
|
作者
ESTEY, E [1 ]
THALL, P [1 ]
ANDREEFF, M [1 ]
BERAN, M [1 ]
KANTARJIAN, H [1 ]
OBRIEN, S [1 ]
ESCUDIER, S [1 ]
ROBERTSON, LE [1 ]
KOLLER, C [1 ]
KORNBLAU, S [1 ]
PIERCE, S [1 ]
FREIREICH, E [1 ]
DEISSEROTH, A [1 ]
KEATING, M [1 ]
机构
[1] UNIV TEXAS,MD ANDERSON CANC CTR,DEPT BIOMATH,HOUSTON,TX
关键词
D O I
10.1200/JCO.1994.12.4.671
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine whether granulocyte colony-stimulating factor (G- CSF) administered before, during, and after fludarabine plus cytarabine (ara- C;FA) chemotherapy affected complete response (CR) rate, infection rate, blood count recovery, or survival in patients with newly diagnosed acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS). Patients and Methods: A total of 112 patients with newly diagnosed AML (n = 69) or MDS (n = 43) received G-CSF 400 μg/m2/d 1 day before (presenting WBC count < 50,000/μL) and/or during (all patients) fludarabine 30 mg/m2/d and ara-C 2 g/m2/d for 5 days (FLAG). G-CSF continued until a CR was achieved. Results were compared with those in 85 newly diagnosed patients (54 AML, 31 MDS) previously treated with FA without G-CSF. Results: Patients in both groups were relatively old (median age of all patients, 63 years), and were likely to have prognostically unfavorable cytogenetic abnormalities (36% had abnormalities of chromosomes 5 and 7 [-5/-7]). G-CSF accelerated recovery to ≥ 1,000 neutrophils (P < .0001; median, 34 days for FA, 21 days for FLAG), but logistic regression provided no evidence that the CR rate was higher with FLAG than with FA (P = .50), with unadjusted CR rates of 63% and 53%, respectively. This may reflect relatively high rates of death before neutrophil recovery in both groups. Rates of infection were similar in both groups. The follow-up duration in remission is short, and much of these data remain censored. To date, survival is similar with FA and FLAG. Conclusion: On average, G-CSF before, during, and after FA had no effect on CR or infection rates in this population, in which elderly patients and poor prognostic factors were prevalent. The use of FA and laminar airflow rooms rather than more usual therapy needs to be considered when analyzing the results.
引用
收藏
页码:671 / 678
页数:8
相关论文
共 50 条
  • [41] Fludarabine, cytosine arabinoside, granulocyte-colony stimulating factor with or without idarubicin in the treatment of high risk acute leukaemia or myelodysplastic syndromes
    Milligan, DW
    Wheatley, K
    Burnett, AK
    BRITISH JOURNAL OF HAEMATOLOGY, 2004, 127 (02) : 238 - 239
  • [42] A PILOT-STUDY OF THE BIOLOGIC AND THERAPEUTIC EFFECTS OF GRANULOCYTE-COLONY-STIMULATING FACTOR (FILGRASTIM) IN PATIENTS WITH ACUTE MYELOGENOUS LEUKEMIA
    JAKUBOWSKI, A
    GORDON, M
    TAFURI, A
    SCHUSTER, S
    ANDREEFF, M
    SHIEH, JH
    VINCENT, M
    GABRILOVE, J
    LEUKEMIA, 1995, 9 (11) : 1799 - 1804
  • [43] Treatment of acute myeloid leukemia and myelodysplastic syndrome with orally administered cytarabine ocfosfate and granulocyte colony-stimulating factor
    Okumura, H
    Yoshida, T
    Takamatsu, H
    Katoh, T
    Murashima, M
    Watanabe, A
    Yamauchi, H
    Matano, S
    Chuhjo, T
    Takeshima, M
    Kaya, H
    Ohtake, S
    Nakamura, S
    Matsuda, T
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 1997, 65 (03) : 263 - 268
  • [44] Prophylactic use of granulocyte colony-stimulating factor after consolidation therapy with high-dose cytarabine for acute myeloid leukemia
    Shadman, Mazyar
    Estey, Elihu H.
    EXPERT REVIEW OF HEMATOLOGY, 2013, 6 (02) : 131 - 133
  • [45] CHRONIC MYELOGENOUS LEUKEMIA (CML) ASSOCIATED WITH GRANULOCYTE-COLONY-STIMULATING FACTOR (G-CSF)-PRODUCING MESOTHELIOMA
    MASUDA, Y
    KIZAKI, M
    UENO, H
    MORI, S
    TAKAYAMA, N
    MUTO, A
    MATSUSHITA, H
    IKEDA, E
    KAWAI, Y
    IKEDA, Y
    LEUKEMIA, 1995, 9 (09) : 1591 - 1594
  • [46] Granulocyte colony-stimulating factor following chemotherapy in elderly patients with newly diagnosed acute myelogenous leukemia
    Maslak, PG
    Weiss, MA
    Berman, E
    Yao, TJ
    Tyson, D
    Golde, DW
    Scheinberg, DA
    LEUKEMIA, 1996, 10 (01) : 32 - 39
  • [47] USE OF RECOMBINANT GRANULOCYTE-COLONY-STIMULATING FACTOR TO TREAT NEUTROPENIA OCCURRING DURING CRANIOSPINAL IRRADIATION
    MACMANUS, MP
    CLARKE, J
    MCCORMICK, D
    ABRAM, WP
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 26 (05): : 845 - 850
  • [48] Fludarabine, Cytarabine, Granulocyte Colony-Stimulating Factor and Melphalan (FALG with L-PAM) as a Reduced Toxicity Conditioning Regimen in Children with Acute Leukemia
    Kato, Koji
    Yoshida, Nao
    Matsumoto, Kimikazu
    Matsuyama, Takaharu
    PEDIATRIC BLOOD & CANCER, 2014, 61 (04) : 712 - 716
  • [49] Low-dose cytarabine, aclarubicin and granulocyte colony-stimulating factor priming regimen versus idarubicin plus cytarabine regimen as induction therapy for older patients with acute myeloid leukemia
    Jin, Jie
    Chen, Jian
    Suo, Shanshan
    Qian, Wenbin
    Meng, Haitao
    Mai, Wenyuan
    Tong, Hongyan
    Huang, Jian
    Yu, Wenjuan
    Wei, Juyin
    Lou, Yinjun
    LEUKEMIA & LYMPHOMA, 2015, 56 (06) : 1691 - 1697
  • [50] COMPLETE REMISSION IN A PATIENT WITH HYPOPLASTIC ACUTE LYMPHOBLASTIC-LEUKEMIA INDUCED BY GRANULOCYTE-COLONY-STIMULATING FACTOR
    HATTA, Y
    IWATA, T
    TAKEUCHI, J
    OHSHIMA, T
    HORIE, T
    ACTA HAEMATOLOGICA, 1995, 94 (01) : 39 - 43