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dc.contributor.author Giebel S
dc.contributor.author Labopin M
dc.contributor.author Potter M
dc.contributor.author Poire X
dc.contributor.author Sengeloev H
dc.contributor.author Socie G
dc.contributor.author Huynh A
dc.contributor.author Afanasyev BV
dc.contributor.author Schanz U
dc.contributor.author Ringden O
dc.contributor.author Kalhs P
dc.contributor.author Beelen DW
dc.contributor.author Campos AM
dc.contributor.author Masszi, Tamás
dc.contributor.author Canaani J
dc.contributor.author Mohty M
dc.contributor.author Nagler A
dc.date.accessioned 2018-10-02T12:35:14Z
dc.date.available 2018-10-02T12:35:14Z
dc.date.issued 2018
dc.identifier.citation pagination=73-81; journalVolume=96; journalTitle=EUROPEAN JOURNAL OF CANCER;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/6310
dc.identifier.uri doi:10.1016/j.ejca.2018.03.018
dc.description.abstract Background: Allogeneic haematopoietic stem cell transplantation (alloHSCT) is considered a standard treatment for patients with Philadelphia chromosome-positive acute lymphoblastic leukaemia (Ph+ ALL) achieving complete remission after induction containing tyrosine kinase inhibitors (TKIs). Methods: We retrospectively compared results of myeloablative alloHSCT from either matched sibling donor (MSD) or unrelated donor (URD) with autologous (auto) HSCT for adults with Ph+ ALL in molecular remission, treated between 2007 and 2014. Results: In univariate analysis, the incidence of relapse at 2 years was 47% after autoHSCT, 28% after MSD-HSCT and 19% after URD-HSCT (P = 0.0002). Respective rates of non-relapse mortality were 2%, 18%, and 22% (P = 0.001). The probabilities of leukaemia-free survival were 52%, 55% and 60% (P = 0.69), while overall survival rates were 70%, 70% and 69% (P = 0.58), respectively. In multivariate analysis, there was a trend towards increased risk of overall mortality after MSD-HSCT (hazard ratio [HR], 1.5, P = 0.12) and URD-HSCT (HR, 1.6, P = 0.08) when referred to autoHSCT. The use of total body irradiation (TBI)-based regimens was associated with reduced risk of relapse (HR, 0.65, P = 0.02) and overall mortality (HR, 0.67, P = 0.01). Conclusion: In the era of TKIs, outcomes of myeloablative autoHSCT and alloHSCT for patients with Ph+ ALL in first molecular remission are comparable. Therefore, autoHSCT appears to be an attractive treatment option potentially allowing for circumvention of alloHSCT sequelae. Irrespective of the type of donor, TBI-based regimens should be considered the preferable type of conditioning for Ph+ ALL. (C) 2018 Elsevier Ltd. All rights reserved.
dc.relation.ispartof urn:issn:0959-8049
dc.title Comparable results of autologous and allogeneic haematopoietic stem cell transplantation for adults with Philadelphia-positive acute lymphoblastic leukaemia in first complete molecular remission: An analysis by the Acute Leukemia Working Party of the EBMT
dc.type Journal Article
dc.date.updated 2018-09-01T09:46:37Z
dc.language.rfc3066 en
dc.identifier.mtmt 3394909
dc.identifier.wos 000432907800009
dc.identifier.pubmed 29679774


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