| Literature DB >> 29468631 |
Nina K Steckel1, Christoph Groth2, Jan-Henrik Mikesch2, Rudolf Trenschel1, Hellmut Ottinger1, Lambros Kordelas1, Carsten Mueller-Tidow3, Christoph Schliemann2, Christian Reicherts2, Joern C Albring2, Gerda Silling2, Eva Schmidt2, Wolfgang E Berdel2,4, Georg Lenz2,4,5, Markus Ditschkowski1, Dietrich W Beelen1, Matthias Stelljes2.
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.Entities:
Keywords: acute myeloid leukaemia; conditioning; haematological malignancies; residual disease; stem cell transplantation
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Year: 2018 PMID: 29468631 DOI: 10.1111/bjh.15137
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998