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急性白血病患儿强化治疗的长期结果

Long-term results of reinforcement therapy in children with acute leukemia.

作者信息

Fernbach D J, George S L, Sutow W W, Ragab A H, Lane D M, Haggard M E, Lonsdale D

出版信息

Cancer. 1975 Nov;36(5):1552-9. doi: 10.1002/1097-0142(197511)36:5<1552::aid-cncr2820360503>3.0.co;2-3.

Abstract

A total of 180 children with acute leukemia was randomized to one of two induction regimens: vincristine plus prednisone, or 6-mercaptopurine plus prednisone. Of 170 patients evaluable for induction therapy, a hematologic remission was achieved in 83% (72/87) on vincristine plus prednisone, and in 93% (77/83) on 6-mercaptopurine plus prednisone. When hematologic remission was achieved, patients were randomized to one of three maintenance schedules: 6-mercaptopurine alone, 6-mercaptopurine plus prednisone for 4 weeks every 3 months, or 6-mercaptopurine plus prednisone plus vincristine for 4 weeks every 3 months. The durations of hematologic remission were compared from the achievement of hematologic remission to bone marrow relapse. The survival data were presented as an overview of the effect of this initial therapy on duration of survival. There was no statistical difference between the two induction regimens. The most important finding in the comparison of the three maintenance schedules was that reinforcement of 6-mercaptopurine maintenance therapy with either prednisone or prednisone plus vincristine resulted in significantly longer durations of remission. Vincristine added to prednisone for reinforcement after induction of remission by vincristine plus prednisone did not increase the duration of hematologic remission or survival over prednisone reinforcement alone.

摘要

总共180名急性白血病患儿被随机分为两种诱导治疗方案之一:长春新碱加泼尼松,或6-巯基嘌呤加泼尼松。在170名可评估诱导治疗的患者中,长春新碱加泼尼松组有83%(72/87)实现血液学缓解,6-巯基嘌呤加泼尼松组为93%(77/83)。实现血液学缓解后,患者被随机分为三种维持治疗方案之一:单独使用6-巯基嘌呤,每3个月使用6-巯基嘌呤加泼尼松4周,或每3个月使用6-巯基嘌呤加泼尼松加长春新碱4周。比较从血液学缓解到骨髓复发的血液学缓解持续时间。生存数据作为初始治疗对生存持续时间影响的概述呈现。两种诱导治疗方案之间无统计学差异。三种维持治疗方案比较中最重要的发现是,用泼尼松或泼尼松加长春新碱强化6-巯基嘌呤维持治疗可显著延长缓解持续时间。在长春新碱加泼尼松诱导缓解后,添加长春新碱至泼尼松进行强化治疗,与单独使用泼尼松强化治疗相比,并未增加血液学缓解持续时间或生存期。

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