Zittoun R, Suciu S, Mandelli F, de Witte T, Thaler J, Stryckmans P, Hayat M, Peetermans M, Cadiou M, Solbu G, Petti M C, Willemze R
Service d'Hématologie, Hôtel-Dieu, Paris, France.
J Clin Oncol. 1996 Jul;14(7):2150-9. doi: 10.1200/JCO.1996.14.7.2150.
To assess the value of granulocyte-macrophage colony-stimulating factor (GM-CSF) for induction treatment of acute myeloid leukemia (AML), both for priming of leukemic cells and for acceleration of hematopoietic recovery.
GM-CSF was administered 5 micrograms/kg/d by continuous intravenous (i.v.) infusion during induction therapy with daunorubicin (DNR) (days 1 to 3) and cytarabine (ARA-C) (days 1 to 7). A total of 102 patients were randomized onto four arms, as follows: (1) GM-CSF 24 hours before and during chemotherapy (arm +/-); (2) GM-CSF after chemotherapy until day 28 or recovery of polymorphonuclear leukocytes (PMNs) (arm -/+);(3) GM-CSF before, during, and after chemotherapy (arm +/+); or (4) no GM-CSF (arm -/-). Stopping rules were applied in case of an initial WBC count greater than 30 x 10(9)/L or a secondary increase of circulating blast cells. Analyses were performed according to the intention-to-treat principle.
The complete remission (CR) rates were 77% (arm -/-), 72% (arm +/-), 48% (arm -/+), and 46% (arm +/+). Patients randomized to receive GM-CSF after induction (arms -/+ and +/+) had a significantly lower CR rate (P = .008) and a trend toward accelerated recovery of neutrophils, but no fewer infections or induction deaths. The lower CR rate appeared to be related to an increased resistance rate, with persistent leukemia. The main side effects of GM-CSF were fluid retention and hypotension.
GM-CSF administered during induction treatment of AML with a DNR/Ara-C combination did not provide any clinical benefit. Furthermore, there was a significant decrease in the CR rate with more persistent leukemia when GM-CSF was administered during the hypoplastic phase after the chemotherapy courses.
评估粒细胞巨噬细胞集落刺激因子(GM-CSF)在急性髓系白血病(AML)诱导治疗中的价值,包括对白血病细胞的启动作用以及加速造血恢复的作用。
在使用柔红霉素(DNR)(第1至3天)和阿糖胞苷(ARA-C)(第1至7天)进行诱导治疗期间,通过持续静脉输注给予GM-CSF,剂量为5微克/千克/天。总共102例患者被随机分为四组,如下:(1)化疗前24小时及化疗期间使用GM-CSF(±组);(2)化疗后使用GM-CSF直至第28天或多形核白细胞(PMN)恢复(-/+组);(3)化疗前、化疗期间及化疗后使用GM-CSF(+/+组);或(4)不使用GM-CSF(-/-组)。如果初始白细胞计数大于30×10⁹/L或循环原始细胞出现二次增加,则应用停药规则。根据意向性治疗原则进行分析。
完全缓解(CR)率分别为77%(-/-组)、72%(±组)、48%(-/+组)和46%(+/+组)。随机接受诱导后使用GM-CSF的患者(-/+组和+/+组)CR率显著较低(P = 0.008),中性粒细胞恢复有加速趋势,但感染或诱导死亡人数并未减少。较低的CR率似乎与耐药率增加及持续性白血病有关。GM-CSF的主要副作用是液体潴留和低血压。
在使用DNR/Ara-C联合方案诱导治疗AML期间给予GM-CSF未带来任何临床益处。此外,在化疗疗程后的造血抑制期给予GM-CSF时,CR率显著降低,白血病更具持续性。