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低剂量阿糖胞苷(LD-AraC)联合粒细胞-巨噬细胞集落刺激因子(rh GM-CSF)治疗骨髓增生异常综合征(MDS)及高白血病风险患者。欧洲癌症研究与治疗组织白血病研究组。

Treatment of myelodysplastic syndromes (MDS) and high leukaemic risk with low-dose cytosine arabinoside (LD-AraC) plus granulocyte-macrophage colony-stimulating factor (rh GM-CSF). The EORTC Leukaemia Group.

作者信息

Gerhartz H H, Marcus R, Delmer A, Zwierzina H, de Witte T, Jacobs A, Visiani G, Fiere D, Sonneveld P, Labar B

机构信息

Medizinische Klinik III, Klinikum Grosshadern, München, Germany.

出版信息

Infection. 1992;20 Suppl 2:S116-23. doi: 10.1007/BF01705030.

Abstract

Symptomatic patients with myelodysplastic syndromes (MDS) and 10-30% blasts in the bone marrow were treated with low-dose AraC (2 x 10 mg/m2 subcutaneously (sc) days 1-14) and GM-CSF (fully glycosylated, Sandoz/Schering-Plough, 2 x 150 micrograms protein/day sc) given either subsequently (days 15-21) or simultaneously (days 8-14 and one week rest). Evaluations were carried out after three courses (nine weeks); responding patients could be continued for two further cycles. Eighty-two patients with refractory anaemia and excess of blasts (RAEB), with (RAEBt) or without transformation, were evaluable: 45 RAEB and 37 RAEBt, mean age 64 years (range 17-80 years). A complete remission was achieved in 14 cases (17%), 11 had a good response (13%), and 12 a partial response (15%). Stable disease was found in 21 cases (26%). There were 12 cases of toxic death (15%), progression was noted in eight patients (10%), and death due to disease in three (4%). No difference existed between the two treatment arms with respect to response. Major adverse events during treatment were haemorrhage (25%), infections (23%), and fever with GM-CSF (21%). GM-CSF did not induce leukaemia nor contribute to haemorrhage induced by AraC, but gave rise to an overall response rate of 46% which is high and relatively durable as compared to other treatments in this disease.

摘要

对有症状的骨髓增生异常综合征(MDS)且骨髓中原始细胞占10%-30%的患者,采用小剂量阿糖胞苷(第1-14天皮下注射2×10mg/m²)和GM-CSF(完全糖基化,山德士/先灵葆雅,每天皮下注射2×150μg蛋白质)进行治疗,GM-CSF要么在随后(第15-21天)给予,要么同时(第8-14天并休息一周)给予。在三个疗程(九周)后进行评估;有反应的患者可继续进行另外两个周期的治疗。82例难治性贫血伴原始细胞增多(RAEB)、有(RAEBt)或无转化的患者可进行评估:45例RAEB和37例RAEBt,平均年龄64岁(范围17-80岁)。14例(17%)达到完全缓解,11例有良好反应(13%),12例有部分反应(15%)。21例(26%)病情稳定。有12例(15%)发生毒性死亡,8例(10%)出现病情进展,3例(4%)死于疾病。两个治疗组在反应方面没有差异。治疗期间的主要不良事件为出血(25%)、感染(23%)以及使用GM-CSF引起的发热(21%)。GM-CSF未诱发白血病,也未加重阿糖胞苷引起的出血,但总体反应率为46%,与该疾病的其他治疗方法相比,这一反应率较高且相对持久。

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