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High-dose melphalan with or without stem cell support before myeloablative allo-SCT for remission induction in patients with advanced relapsed or refractory AML.
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1195174
Author(s) O'Meara, A; Pabst, T; Heim, D; Gerull, S; Bucher, C; Halter, J; Arber, C; Rovò, A; Tichelli, A; Gratwohl, A; Stern, M
Author(s) at UniBasel Tichelli, André
Rovó, Alicia
Arber Barth, Caroline
Heim, Dominik A.
Stern, Martin Andreas
Year 2011
Title High-dose melphalan with or without stem cell support before myeloablative allo-SCT for remission induction in patients with advanced relapsed or refractory AML.
Journal Bone marrow transplantation
Volume 46
Number 5
Pages / Article-Number 636-40
Keywords AML, melphalan, auto-SCT, allo-SCT
Abstract Treatment strategies for relapsed/refractory AML are limited and disappointing. Recently, high-dose melphalan (HDM) chemotherapy and autologous hematopoietic SCT (HSCT) has been proposed for AML re-induction. We investigated the impact of HDM remission induction in highly advanced relapsed/refractory AML patients planned for allogeneic HSCT. A total of 23 patients with relapsed/refractory AML were prospectively scheduled for HDM with or without stem cell support followed by myeloablative allogeneic HSCT. Patients included nine individuals with a history of previous HSCT (seven allogeneic, two autologous). A total of 18 patients (78%) achieved a leukemia-free state and an additional four had substantial reduction of the initial leukemia burden warranting treatment continuation. There were no differences between patients with or without immediate stem cell support regarding mucositis or other organ toxicity. A total of 20 patients proceeded to myeloablative allogeneic HSCT. Outcome of allogeneic HSCT was poor: 11 patients (55%) relapsed, 7 patients (35%) died from TRM and only 2 patients (10%) were alive at the last follow-up. Our study shows that HDM is effective in inducing a leukemia-free state in patients with highly advanced relapsed/refractory AML. Leukemia burden reduction with HDM, however, did not translate into improved OS.
Publisher Nature Publishing Group
ISSN/ISBN 0268-3369
edoc-URL http://edoc.unibas.ch/dok/A6005360
Full Text on edoc No
Digital Object Identifier DOI 10.1038/bmt.2010.181
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/20697364
ISI-Number WOS:000290472500002
Document type (ISI) Article
 
   

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