Castaigne S, Chevret S, Lepage E, Guilhot F, Fenaux P, Bordessoule D, Tilly H, Auzanneau G, Tertian G, Guy H
Department of Hematology, Hôpital Saint-Louis, Paris, France.
Nouv Rev Fr Hematol (1978). 1990;32(5):297-300.
705 children and adults patients with de novo acute nonlymphoblastic leukemia were entered from 1981 to 1989 into 2 prospectives multicenter trials: 01AM81 and 01AM86. They received an intensive induction course with Rubidazone 200 mg/sqm/day x 4 days and cytosine arabinoside 200 mg/sqm/day x 7 days, then 3 consolidation courses at outpatients, and a maintenance treatment. Total duration of therapy was 3 years. The overall complete remission rate was 80%. The median overall survival time was 19 months and the 5-year survival rate is 26%. The median remission duration for the 568 remitters was 18 months and the 5-year first remission rate is 30%. Prognostic factors for the remission rate were age, initial leukocytosis, FAB subtype. Prognostic factors for remission duration were the delay until CR, initial leukocytosis and karyotype.
1981年至1989年期间,705例初发急性非淋巴细胞白血病患儿及成年患者被纳入两项前瞻性多中心试验:01AM81和01AM86。他们接受了强化诱导疗程,柔红霉素200mg/平方米/天,共4天,阿糖胞苷200mg/平方米/天,共7天,然后在门诊进行3个巩固疗程以及维持治疗。治疗总时长为3年。总体完全缓解率为80%。中位总生存时间为19个月,5年生存率为26%。568例缓解者的中位缓解持续时间为18个月,5年首次缓解率为30%。缓解率的预后因素为年龄、初始白细胞增多、FAB亚型。缓解持续时间的预后因素为达到完全缓解的延迟时间、初始白细胞增多及核型。