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AIDA 0493 方案治疗初发急性早幼粒细胞白血病:极长期结果和维持治疗的作用。

AIDA 0493 protocol for newly diagnosed acute promyelocytic leukemia: very long-term results and role of maintenance.

机构信息

Unità Operativa Complessa di Ematologia e Terapia Cellulare, Università Campus Bio-Medico, Roma, Italy.

出版信息

Blood. 2011 May 5;117(18):4716-25. doi: 10.1182/blood-2010-08-302950. Epub 2011 Mar 8.

Abstract

All-trans-retinoic acid (ATRA) has greatly modified the prognosis of acute promyelocytic leukemia; however, the role of maintenance in patients in molecular complete remission after consolidation treatment is still debated. From July 1993 to May 2000, 807 genetically proven newly diagnosed acute promyelocytic leukemia patients received ATRA plus idarubicin as induction, followed by 3 intensive consolidation courses. Thereafter, patients reverse-transcribed polymerase chain reaction-negative for the PML-RARA fusion gene were randomized into 4 arms: oral 6-mercaptopurine and intramuscular methotrexate (arm 1); ATRA alone (arm 2); 3 months of arm1 alternating to 15 days of arm 2 (arm 3); and no further therapy (arm 4). Starting from February 1997, randomization was limited to ATRA-containing arms only (arms 2 and 3). Complete remission was achieved in 761 of 807 (94.3%) patients, and 681 completed the consolidation program. Of these, 664 (97.5%) were evaluated for the PML-RARA fusion gene, and 586 of 646 (90.7%) who tested reverse-transcribed polymerase chain reaction-negative were randomized to maintenance. The event-free survival estimate at 12 years was 68.9% (95% confidence interval, 66.4%-71.4%), and no differences in disease-free survival at 12 years were observed among the maintenance arms.

摘要

全反式维甲酸(ATRA)极大地改善了急性早幼粒细胞白血病的预后;然而,在巩固治疗后分子完全缓解的患者中进行维持治疗的作用仍存在争议。1993 年 7 月至 2000 年 5 月,807 例经基因证实的新发急性早幼粒细胞白血病患者接受 ATRA 联合伊达比星作为诱导治疗,随后进行 3 个强化巩固治疗疗程。此后,逆转录聚合酶链反应(PCR)阴性的 PML-RARA 融合基因患者被随机分为 4 组:口服 6-巯基嘌呤和肌肉注射甲氨蝶呤(第 1 组);单独使用 ATRA(第 2 组);第 1 组治疗 3 个月与第 2 组治疗 15 天交替(第 3 组);和无进一步治疗(第 4 组)。从 1997 年 2 月开始,随机分组仅限于包含 ATRA 的组(第 2 组和第 3 组)。807 例患者中有 761 例(94.3%)达到完全缓解,且 681 例完成巩固治疗方案。其中,664 例(97.5%)接受 PML-RARA 融合基因评估,646 例逆转录 PCR 阴性患者中 586 例被随机分配到维持治疗组。12 年时无事件生存估计值为 68.9%(95%置信区间,66.4%-71.4%),且在 12 年时各维持治疗组之间无疾病无进展生存差异。

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