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急性早幼粒细胞白血病患者的治疗。欧洲癌症研究与治疗组织白血病协作组的经验。欧洲癌症研究与治疗组织白血病协作组

Treatment of patients with acute promyelocytic leukemia. The EORTC-LCG experience. EORTC Leukemia Cooperative Group.

作者信息

Willemze R, Suciu S, Mandelli F, de Witte T, Cadiou M, Castoldi G L, Liso V, Dardenne M, Solbu G, Zittoun R

机构信息

Department of Hematology, Leiden University, The Netherlands.

出版信息

Leukemia. 1994;8 Suppl 2:S48-55.

PMID:7815837
Abstract

Acute promyelocytic leukemia (M3) is, as one of the FAB subtypes of AML, included in the EORTC/GIMEMA AML-8A and 8B randomized trials. In these trials 1519 patients were included, 477 of them in non-Italian EORTC-LCG centers and 1042 in GIMEMA centers. A total of 80 patients were classified as M3 including 18 patients with M3-variant. Thirty-nine were male and 41 female. Ages ranged from 15 to 59 years; 25 (31.3%) of them were younger than 30, 34 (42.5%) between 30 and 45, and 21 (26.3%) older than 45 years of age. 56.3% of the patients had leukocytes less than 5 x 10(9)/l at the time of diagnosis vs. 24.9% of the patients belonging to the other FAB subtypes. Remission induction consisted of a standard protocol with 3 days daunorubicin and 7 days of cytosine arabinoside. Forty-three patients (53.8%) achieved a complete remission compared to 64.6% of the remaining AML patients. After salvage treatment this percentage increased to 70%, which is the same as for the other AML subtypes. Thirteen (16.3%) patients died during remission induction, mainly due to hemorrhagic complications. This percentage is significantly higher than the death rate (9.1%) in the other FAB subtypes of AML. All patients received one course of consolidation treatment. Post consolidation treatment could be either standard maintenance, intensive consolidation courses, autologous or allogeneic transplantation, according to the guidelines of the treatment protocols. At present, relapses almost all in the bone marrow, are seen in only 34.9% of the M3 patients, compared to 48.4% in the remaining AML patients. Disease-free survival for patients less than 45 years of age with the M2 and M3 subtypes was approximately 50% at 3 years compared to 30-40% for the other FAB subtypes. Despite the higher death rate during induction, the long-term survival results were better for M3 patients in comparison with the remaining AML patients. The projected survival at 3 years was 50% for M3 patients vs. 38% for remaining patients.

摘要

急性早幼粒细胞白血病(M3)作为急性髓系白血病(AML)的FAB亚型之一,被纳入欧洲癌症研究与治疗组织(EORTC)/意大利成人白血病研究组(GIMEMA)的AML-8A和8B随机试验。在这些试验中,共纳入了1519例患者,其中477例在非意大利的EORTC-LCG中心,1042例在GIMEMA中心。共有80例患者被分类为M3,其中包括18例M3变异型患者。39例为男性,41例为女性。年龄范围为15至59岁;其中25例(31.3%)年龄小于30岁,34例(42.5%)年龄在30至45岁之间,21例(26.3%)年龄大于45岁。56.3%的患者在诊断时白细胞计数低于5×10⁹/L,而其他FAB亚型患者的这一比例为24.9%。缓解诱导采用标准方案,即3天柔红霉素和7天阿糖胞苷。43例(53.8%)患者实现完全缓解,而其余AML患者的这一比例为64.6%。经过挽救治疗后,这一比例增至70%,与其他AML亚型相同。13例(16.3%)患者在缓解诱导期间死亡,主要死于出血并发症。这一比例显著高于其他FAB亚型AML的死亡率(9.1%)。所有患者均接受了一个疗程的巩固治疗。巩固治疗后可根据治疗方案指南进行标准维持治疗、强化巩固疗程、自体或异体移植。目前,几乎所有复发都发生在骨髓,M3患者的复发率仅为34.9%,而其余AML患者的复发率为48.4%。M2和M3亚型中年龄小于45岁患者的3年无病生存率约为50%,而其他FAB亚型为30%-40%。尽管诱导期间死亡率较高,但与其余AML患者相比,M3患者的长期生存结果更好。M3患者的3年预计生存率为50%,其余患者为38%。

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