Department of Clinical Haematology, Peter MacCallum Cancer Centre and The Royal Melbourne Hospital, Melbourne, Australia.
Department of Pharmacy, The Royal Melbourne Hospital, Parkville, Australia.
Leuk Lymphoma. 2023 Dec;64(13):2123-2132. doi: 10.1080/10428194.2023.2251071. Epub 2023 Sep 1.
High-dose cytarabine (HDAC) is conventionally delivered on days 1, 3 and 5 (HDAC-135) as acute myeloid leukemia (AML) post-remission therapy. Limited data is available on alternative HDAC schedules such as HDAC-123 (given consecutively for 3 days). We retrospectively compared the tolerability and efficacy of HDAC-135 and HDAC-123 delivered in sequential cohorts of adult AML patients. Seventy-three patients were included with 33% aged ≥60 years. HDAC-123 was associated with faster hematological recovery, reduced bacteremia and shorter hospitalization. No differences in safety profile or hematological recovery were seen between patients ≥60 years and <60 years receiving HDAC-123 except a shorter median time to neutrophil count recovery after cycle 1 in the latter group. Three patients (8%) receiving HDAC-123, all aged <60 years, required a change in schedule to HDAC-135 due to transient cytarabine-related side effects. HDAC-123 consolidation was well-tolerated by AML patients, including those ≥60 years, and associated with tangible reductions in resource utilization.
高剂量阿糖胞苷(HDAC)通常在缓解后作为急性髓细胞白血病(AML)的治疗方案,在第 1、3 和 5 天(HDAC-135)给予。关于替代 HDAC 方案(如连续 3 天给予 HDAC-123)的数据有限。我们回顾性比较了连续队列中成人 AML 患者接受 HDAC-135 和 HDAC-123 的耐受性和疗效。共纳入 73 例患者,其中 33%的患者年龄≥60 岁。HDAC-123 与更快的血液学恢复、减少菌血症和缩短住院时间相关。在接受 HDAC-123 的年龄≥60 岁和<60 岁的患者之间,除了后者组在第 1 周期后中性粒细胞计数恢复的中位时间较短外,在安全性特征或血液学恢复方面没有差异。由于短暂的阿糖胞苷相关副作用,3 名(8%)接受 HDAC-123 的患者(均<60 岁)需要更改方案至 HDAC-135。HDAC-123 巩固治疗 AML 患者,包括年龄≥60 岁的患者,耐受性良好,且与资源利用的显著减少相关。