Goldberg J, Gryn J, Raza A, Bennett J, Browman G, Bryant J, Grunwald H, Larson R, Vogler R, Preisler H
Cooper University Medical Center, Camden, New Jersey 08103.
Am J Hematol. 1993 Aug;43(4):286-90. doi: 10.1002/ajh.2830430411.
In an effort to determine if cell cycle active agents are augmented when given after non-cell cycle active agents, 104 patients with either multiply relapsed or refractory acute nonlymphocytic leukemia or blast crisis of chronic myelogenous leukemia were treated with mitoxantrone. Patients whose bone marrow did not show significant cytoreduction received 5-azacytidine. Twenty-seven of the 93 evaluable patients (23%) with ANLL achieved a complete remission. A total of 28% of patients receiving mitoxantrone alone achieved remission compared to 15% for those receiving mitoxantrone and 5-azacytidine. Relapsed patients had a higher CR rate (36%) than refractory patients (15%). Nausea, vomiting, and stomatitis were common but rarely severe. The median duration of remission was 3.7 months and patients with abnormal karyotypes had longer remission durations than those with normal karyotypes. In this patient population, there was no evidence that 5-azacytidine given after mitoxantrone increased the complete remission rate.
为了确定细胞周期活性药物在非细胞周期活性药物之后使用时是否会增强疗效,104例复发多次或难治的急性非淋巴细胞白血病或慢性粒细胞白血病急变期患者接受了米托蒽醌治疗。骨髓未显示明显细胞减少的患者接受了5-氮杂胞苷治疗。93例可评估的急性非淋巴细胞白血病患者中有27例(23%)获得完全缓解。单独接受米托蒽醌治疗的患者中共有28%获得缓解,而接受米托蒽醌和5-氮杂胞苷治疗的患者为15%。复发患者的完全缓解率(36%)高于难治患者(15%)。恶心、呕吐和口腔炎很常见,但很少严重。缓解期的中位数为3.7个月,核型异常的患者缓解期比核型正常的患者更长。在该患者群体中,没有证据表明米托蒽醌后给予5-氮杂胞苷会提高完全缓解率。