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