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T-cell-replete haploidentical transplantation versus autologous stem cell transplantation in adult acute leukemia: a matched pair analysis

Adult patients with acute leukemia in need of a transplant but without a genoidentical donor are usually considered upfront for transplantation with stem cells from any other allogeneic source, rather than autologous stem cell transplantation. We used data from the European Society for Blood and Mar...

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Bibliographic Details
Published in:Haematologica (Roma) 2015-04, Vol.100 (4), p.558-564
Main Authors: Gorin, Norbert-Claude, Labopin, Myriam, Piemontese, Simona, Arcese, William, Santarone, Stella, Huang, He, Meloni, Giovanna, Ferrara, Felicetto, Beelen, Dietrich, Sanz, Miguel, Bacigalupo, Andrea, Ciceri, Fabio, Mailhol, Audrey, Nagler, Arnon, Mohty, Mohamad
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Language:English
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Summary:Adult patients with acute leukemia in need of a transplant but without a genoidentical donor are usually considered upfront for transplantation with stem cells from any other allogeneic source, rather than autologous stem cell transplantation. We used data from the European Society for Blood and Marrow Transplantation and performed a matched pair analysis on 188 T-cell-replete haploidentical and 356 autologous transplants done from January 2007 to December 2012, using age, diagnosis, disease status, cytogenetics, and interval from diagnosis to transplant as matching factors. "Haploidentical expert" centers were defined as having reported more than five haploidentical transplants for acute leukemia (median value for the study period). The median follow-up was 28 months. Multivariate analyses, including type of transplant categorized into three classes ("haploidentical regular", "haploidentical expert" and autologous), conditioning intensity (reduced intensity versus myeloablative conditioning) and the random effect taking into account associations related to matching, showed that non-relapse mortality was higher following haploidentical transplants in expert (HR: 4.7; P=0.00004) and regular (HR: 8.98; P
ISSN:0390-6078
1592-8721
DOI:10.3324/haematol.2014.111450