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大剂量马法兰序贯预处理化疗联合异基因造血干细胞移植治疗复发或难治性急性髓系白血病的成人患者。

High-dose melphalan-based sequential conditioning chemotherapy followed by allogeneic haematopoietic stem cell transplantation in adult patients with relapsed or refractory acute myeloid leukaemia.

机构信息

Department of Bone Marrow Transplantation, West German Cancer Centre, University Hospital of Essen, Essen, Germany.

Department of Medicine A, University Hospital of Muenster, Muenster, Germany.

出版信息

Br J Haematol. 2018 Mar;180(6):840-853. doi: 10.1111/bjh.15137. Epub 2018 Feb 21.

DOI:10.1111/bjh.15137
PMID:29468631
Abstract

Considering the unsatisfactory results of salvage therapies for patients with relapsed/refractory acute myeloid leukaemia (R/R-AML), their value before allogeneic haematopoietic stem cell transplantation (HSCT) remains questionable. However, direct allogeneic HSCT following established conditioning regimens applied in patients with R/R-AML during active disease has been equally disappointing. In this retrospective observational study, high-dose melphalan, as part of a sequential preparative regimen, followed by a total body irradiation (4 × 2 Gy)-based or a treosulfan-based dose-adapted conditioning therapy for allogeneic HSCT was administered to 292 adult patients (median age 56 years, range 17-74) with primary refractory (144 patients), secondary refractory (97 patients) or relapsed AML (51 patients). Overall survival rates at 3 years were 34%, 29% and 41%, respectively. Risk factors associated with an inferior survival were higher age, transplantation from a human leucocyte antigen-mismatched donor and high disease burden. Patients transplanted with blast infiltration <20% showed a notable survival rate of 51% at 3 years. In particular, patients with primary refractory AML showed a more favourable outcome when transplanted early during their disease course. Thus, high-dose melphalan-based sequential conditioning chemotherapy followed by an allogeneic HSCT is feasible and enables long-term remission to be achieved in a substantial proportion of patients with active R/R-AML.

摘要

考虑到复发/难治性急性髓系白血病 (R/R-AML) 患者挽救治疗的结果不理想,其在异基因造血干细胞移植 (HSCT) 前的价值仍存在疑问。然而,在活动性疾病期间,对 R/R-AML 患者应用既定的预处理方案后直接进行异基因 HSCT 的效果同样令人失望。在这项回顾性观察性研究中,高剂量美法仑作为序贯预处理方案的一部分,随后进行全身照射 (4×2 Gy) 或基于三氟尿苷的剂量适应预处理治疗,用于 292 名成人患者(中位年龄 56 岁,范围 17-74 岁),包括原发性难治(144 例)、继发性难治(97 例)或复发 AML(51 例)。3 年总生存率分别为 34%、29%和 41%。与生存不良相关的危险因素包括年龄较大、HLA 错配供体移植和疾病负担较高。移植时白血病浸润<20%的患者 3 年生存率显著,为 51%。特别是原发性难治性 AML 患者在疾病早期进行移植时,预后更有利。因此,高剂量美法仑为基础的序贯预处理化疗后进行异基因 HSCT 是可行的,可使相当一部分活动性 R/R-AML 患者获得长期缓解。

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