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移植前诱导和巩固周期对 AML 异基因移植结局的影响:CIBMTR 在 3113 例 AML 患者中的分析。

Impact of pre-transplant induction and consolidation cycles on AML allogeneic transplant outcomes: a CIBMTR analysis in 3113 AML patients.

机构信息

University of Pittsburgh, Pittsburgh, PA, USA.

CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Leukemia. 2023 May;37(5):1006-1017. doi: 10.1038/s41375-022-01738-3. Epub 2022 Oct 30.

Abstract

We investigated the impact of the number of induction/consolidation cycles on outcomes of 3113 adult AML patients who received allogeneic hematopoietic cell transplantation (allo-HCT) between 2008 and 2019. Patients received allo-HCT using myeloablative (MAC) or reduced-intensity (RIC) conditioning in first complete remission (CR) or with primary induction failure (PIF). Patients who received MAC allo-HCT in CR after 1 induction cycle had 1.3-fold better overall survival (OS) than 2 cycles to CR and 1.47-fold better than ≥3 cycles. OS after CR in 2 or ≥3 cycles was similar. Relapse risk was 1.65-fold greater in patients receiving ≥3 cycles to achieve CR. After RIC allo-HCT, the number of induction cycles to CR did not affect OS. Compared to CR in 1 cycle, relapse risk was 1.24-1.41-fold greater in patients receiving 2 or ≥3 cycles. For patients receiving only 1 cycle to CR, consolidation therapy prior to MAC allo-HCT was associated with improved OS vs. no consolidation therapy. Detectable MRD at the time of MAC allo-HCT did not impact outcomes while detectable MRD preceding RIC allo-HCT was associated with an increased risk of relapse. For allo-HCT in PIF, OS was significantly worse than allo-HCT in CR after 1-3 cycles.

摘要

我们研究了 2008 年至 2019 年间接受同种异体造血细胞移植 (allo-HCT) 的 3113 例成人 AML 患者的诱导/巩固周期数量对其结局的影响。患者在首次完全缓解 (CR) 或原发性诱导失败 (PIF) 时接受了清髓性 (MAC) 或减低强度 (RIC) 预处理的 allo-HCT。在 CR 中接受 1 个诱导周期的 MAC allo-HCT 的患者的总生存率 (OS) 比 2 个周期的患者好 1.3 倍,比≥3 个周期的患者好 1.47 倍。在 2 个或≥3 个周期的 CR 后 OS 相似。达到 CR 时接受≥3 个周期治疗的患者复发风险增加 1.65 倍。在接受 RIC allo-HCT 后,达到 CR 的诱导周期数量不会影响 OS。与 1 个周期的 CR 相比,接受 2 个或≥3 个周期治疗的患者的复发风险增加了 1.24-1.41 倍。对于仅接受 1 个周期达到 CR 的患者,MAC allo-HCT 前的巩固治疗与无巩固治疗相比,OS 得到改善。MAC allo-HCT 时可检测到 MRD 并不影响结局,而 RIC allo-HCT 前可检测到 MRD 与复发风险增加相关。对于 PIF 中的 allo-HCT,其 OS 明显差于 1-3 个周期后 CR 中的 allo-HCT。

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