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异基因造血细胞移植治疗晚期系统性肥大细胞增生症:DRST 和 GREM 注册研究的回顾性分析。

Allogeneic Hematopoietic Cell Transplantation in Advanced Systemic Mastocytosis: A retrospective analysis of the DRST and GREM registries.

机构信息

Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.

Department of Oncology, Hematology, Hemostaseology and Stem Cell Transplantation, University Hospital RWTH Aachen, Aachen, Germany & Center for Integrated Oncology (CIO), Aachen, Bonn, Cologne, Düsseldorf (ABCD), Aachen, Germany.

出版信息

Leukemia. 2024 Apr;38(4):810-821. doi: 10.1038/s41375-024-02186-x. Epub 2024 Mar 6.

Abstract

We identified 71 patients with AdvSM (aggressive SM [ASM], SM with an associated hematologic neoplasm [SM-AHN, e.g., acute myeloid leukemia, SM-AML], mast cell leukemia [MCL]) in two national registries (DRST/GREM) who received an allogeneic hematopoietic cell transplantation (alloHCT) performed in Germany from 1999-2021. Median overall survival (OS) of ASM/SM-AHN (n = 30, 45%), SM-AML (n = 28, 39%) and MCL ± AHN (n = 13, 19%) was 9.0, 3.3 and 0.9 years (P = 0.007). Improved median OS was associated with response of SM (17/41, 41%; HR 0.4 [0.2-0.9], P = 0.035) and/or of AHN (26/43, 60%, HR 0.3 [0.1-0.7], P = 0.004) prior to alloHCT. Adverse predictors for OS included absence of KIT D816V (10/61, 16%, HR 2.9 [1.2-6.5], P < 0.001) and a complex karyotype (9/60, 15%, HR 4.2 [1.8-10.0], P = 0.016). HLA-match, conditioning type or transplantation at centers reporting above-average alloHCTs (≥7) had no impact on OS. Taking into account competing events at years 1, 3 and 5, relapse-related mortality and non-relapse mortality rate were 15%/23%, 20%/30% and 23%/35%, respectively. Irrespective of subtype, subsequent treatment response was achieved in 13/30 (43%) patients and was highest on midostaurin/avapritinib (7/9, 78%). We conclude that outcome of alloHCT in AdvSM is more affected by disease phenotype and treatment response prior to transplant than by transplant characteristics.

摘要

我们在两个国家登记处(DRST/GREM)中确定了 71 名接受异基因造血细胞移植(alloHCT)的 AdvSM 患者(侵袭性 SM [ASM],伴相关血液系统肿瘤的 SM [SM-AHN,例如急性髓系白血病,SM-AML],肥大细胞白血病 [MCL]),alloHCT 于 1999 年至 2021 年在德国进行。ASM/SM-AHN(n=30,45%)、SM-AML(n=28,39%)和 MCL±AHN(n=13,19%)的中位总生存期(OS)分别为 9.0、3.3 和 0.9 年(P=0.007)。SM(41%,HR 0.4 [0.2-0.9],P=0.035)和/或 AHN(60%,HR 0.3 [0.1-0.7],P=0.004)缓解与改善的中位 OS 相关在 alloHCT 之前。OS 的不良预测因素包括缺乏 KIT D816V(10/61,16%,HR 2.9 [1.2-6.5],P<0.001)和复杂核型(15%,HR 4.2 [1.8-10.0],P=0.016)。HLA 匹配、预处理类型或在报告 alloHCT 高于平均值(≥7)的中心进行移植对 OS 没有影响。考虑到第 1、3 和 5 年的竞争事件,与复发相关的死亡率和非复发死亡率分别为 15%/23%、20%/30%和 23%/35%。无论亚型如何,30 名患者中有 13 名(43%)获得了后续治疗反应,其中米哚妥林/阿伐替尼(7/9,78%)的反应最高。我们得出的结论是,alloHCT 在 AdvSM 中的结果受疾病表型和移植前治疗反应的影响大于移植特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea7/10997505/6c6a02b66b89/41375_2024_2186_Fig1_HTML.jpg

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