Leukemia Research Center, Saiseikai Maebashi Hospital, Maebashi, Japan.
Blood. 2011 Feb 24;117(8):2366-72. doi: 10.1182/blood-2010-07-295279. Epub 2010 Dec 29.
We conducted a prospective randomized study to assess the optimal postremission therapy for adult acute myeloid leukemia in patients younger than 65 years in the first complete remission. A total of 781 patients in complete remission were randomly assigned to receive consolidation chemotherapy of either 3 courses of high-dose cytarabine (HiDAC, 2 g/m(2) twice daily for 5 days) alone or 4 courses of conventional standard-dose multiagent chemotherapy (CT) established in the previous JALSG AML97 study. Five-year disease-free survival was 43% for the HiDAC group and 39% for the multiagent CT group (P = .724), and 5-year overall survival was 58% and 56%, respectively (P = .954). Among the favorable cytogenetic risk group (n = 218), 5-year disease-free survival was 57% for HiDAC and 39% for multiagent CT (P = .050), and 5-year overall survival was 75% and 66%, respectively (P = .174). In the HiDAC group, the nadir of leukocyte counts was lower, and the duration of leukocyte less than 1.0 × 10(9)/L longer, and the frequency of documented infections higher. The present study demonstrated that the multiagent CT regimen is as effective as our HiDAC regimen for consolidation. Our HiDAC regimen resulted in a beneficial effect on disease-free survival only in the favorable cytogenetic leukemia group. This trial was registered at www.umin.ac.jp/ctr/ as #C000000157.
我们进行了一项前瞻性随机研究,旨在评估 65 岁以下成人急性髓系白血病患者在首次完全缓解后的最佳缓解后治疗方案。共有 781 例完全缓解的患者被随机分为两组,一组接受高剂量阿糖胞苷(HiDAC,2 g/m(2),每日 2 次,连用 5 天)巩固化疗,另一组接受之前 JALSG AML97 研究中确立的 4 个疗程常规标准剂量多药化疗(CT)。HiDAC 组的 5 年无病生存率为 43%,多药 CT 组为 39%(P =.724),5 年总生存率分别为 58%和 56%(P =.954)。在有利的细胞遗传学风险组(n = 218)中,HiDAC 组的 5 年无病生存率为 57%,多药 CT 组为 39%(P =.050),5 年总生存率分别为 75%和 66%(P =.174)。HiDAC 组白细胞计数的最低点较低,白细胞计数小于 1.0×10(9)/L 的持续时间较长,且有记录的感染频率较高。本研究表明,多药 CT 方案与我们的 HiDAC 方案在巩固治疗方面同样有效。我们的 HiDAC 方案仅在有利细胞遗传学白血病组中对无病生存率产生有益影响。该试验在 www.umin.ac.jp/ctr/ 注册,编号为 #C000000157。