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