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Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS

We have retrospectively compared survivals between acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) patients who received either a clofarabine/busulfan (CloB2A2) or a fludarabine/busulfan (FB2A2) RIC regimen for allogeneic stem cell transplantation. Between 2009 and 2014, 355 allotranspla...

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Autores principales: Chevallier, Patrice, Labopin, Myriam, de La Tour, Regis Peffault, Lioure, Bruno, Bulabois, Claude‐Eric, Huynh, Anne, Blaise, Didier, Turlure, Pascal, Daguindau, Etienne, Maillard, Natacha, Yakoub‐Agha, Ibrahim, Guillerm, Gaelle, Delage, Jeremy, Contentin, Nathalie, Bay, Jacques‐Olivier, Beckerich, Florence, Bourhis, Jean‐Henri, Detrait, Marie, Vigouroux, Stéphane, François, Sylvie, Legrand, Faezeh, Guillaume, Thierry, Mohty, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119961/
https://www.ncbi.nlm.nih.gov/pubmed/27748046
http://dx.doi.org/10.1002/cam4.880
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author Chevallier, Patrice
Labopin, Myriam
de La Tour, Regis Peffault
Lioure, Bruno
Bulabois, Claude‐Eric
Huynh, Anne
Blaise, Didier
Turlure, Pascal
Daguindau, Etienne
Maillard, Natacha
Yakoub‐Agha, Ibrahim
Guillerm, Gaelle
Delage, Jeremy
Contentin, Nathalie
Bay, Jacques‐Olivier
Beckerich, Florence
Bourhis, Jean‐Henri
Detrait, Marie
Vigouroux, Stéphane
François, Sylvie
Legrand, Faezeh
Guillaume, Thierry
Mohty, Mohamad
author_facet Chevallier, Patrice
Labopin, Myriam
de La Tour, Regis Peffault
Lioure, Bruno
Bulabois, Claude‐Eric
Huynh, Anne
Blaise, Didier
Turlure, Pascal
Daguindau, Etienne
Maillard, Natacha
Yakoub‐Agha, Ibrahim
Guillerm, Gaelle
Delage, Jeremy
Contentin, Nathalie
Bay, Jacques‐Olivier
Beckerich, Florence
Bourhis, Jean‐Henri
Detrait, Marie
Vigouroux, Stéphane
François, Sylvie
Legrand, Faezeh
Guillaume, Thierry
Mohty, Mohamad
author_sort Chevallier, Patrice
collection PubMed
description We have retrospectively compared survivals between acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) patients who received either a clofarabine/busulfan (CloB2A2) or a fludarabine/busulfan (FB2A2) RIC regimen for allogeneic stem cell transplantation. Between 2009 and 2014, 355 allotransplanted cases were identified from the SFGM‐TC registry as having received either the FB2A2 (n = 316, 56% males, median age: 59.2 years, AML 78.5%, first complete remission [CR1] 72%, median follow‐up: 20 months) or the CloB2A2 (n = 39, 62% males, median age: 60.8 years, AML 62%, CR1 69%, median follow‐up: 22.4 months) RIC regimen. In multivariate analysis, FB2A2 was associated with significant lower overall survival (OS, HR: 2.14; 95%CI: 1.05–4.35, P = 0.04) and higher relapse incidence (RI, HR: 2.17; 95%CI: 1.02–4.61, P = 0.04) and a trend for lower leukemia‐free survival (LFS, HR: 1.75; 95%CI: 0.94–3.26, P = 0.08). These results were confirmed using a propensity score‐matching strategy. However, when considering AML and MDS patients separately, the benefit of the CLOB2A2 regimen was restricted to AML patients (2‐year OS FB2A2: 38% [14.5–61.6] vs. CloB2A2: 79.2% [62.9–95.4], P = 0.01; 2‐year LFS FB2A2: 38% [16–59.9] vs. CloB2A2: 70.8% [52.6–89], P = 0.03). The better survivals were due to the lower risk of relapse in this CloB2A2 AML subgroup (2‐year RI FB2A2: 41.2% [19–62.4] vs. CloB2A2: 16.7% [5–34.2], P = 0.05). This retrospective comparison suggests that the CloB2A2 RIC regimen can likely provide longer survival than that awarded by a FB2A2 RIC regimen and may become a new standard of care RIC regimen for allotransplanted AML patients. A prospective phase 3 randomized study is warranted.
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spelling pubmed-51199612016-11-28 Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS Chevallier, Patrice Labopin, Myriam de La Tour, Regis Peffault Lioure, Bruno Bulabois, Claude‐Eric Huynh, Anne Blaise, Didier Turlure, Pascal Daguindau, Etienne Maillard, Natacha Yakoub‐Agha, Ibrahim Guillerm, Gaelle Delage, Jeremy Contentin, Nathalie Bay, Jacques‐Olivier Beckerich, Florence Bourhis, Jean‐Henri Detrait, Marie Vigouroux, Stéphane François, Sylvie Legrand, Faezeh Guillaume, Thierry Mohty, Mohamad Cancer Med Clinical Cancer Research We have retrospectively compared survivals between acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) patients who received either a clofarabine/busulfan (CloB2A2) or a fludarabine/busulfan (FB2A2) RIC regimen for allogeneic stem cell transplantation. Between 2009 and 2014, 355 allotransplanted cases were identified from the SFGM‐TC registry as having received either the FB2A2 (n = 316, 56% males, median age: 59.2 years, AML 78.5%, first complete remission [CR1] 72%, median follow‐up: 20 months) or the CloB2A2 (n = 39, 62% males, median age: 60.8 years, AML 62%, CR1 69%, median follow‐up: 22.4 months) RIC regimen. In multivariate analysis, FB2A2 was associated with significant lower overall survival (OS, HR: 2.14; 95%CI: 1.05–4.35, P = 0.04) and higher relapse incidence (RI, HR: 2.17; 95%CI: 1.02–4.61, P = 0.04) and a trend for lower leukemia‐free survival (LFS, HR: 1.75; 95%CI: 0.94–3.26, P = 0.08). These results were confirmed using a propensity score‐matching strategy. However, when considering AML and MDS patients separately, the benefit of the CLOB2A2 regimen was restricted to AML patients (2‐year OS FB2A2: 38% [14.5–61.6] vs. CloB2A2: 79.2% [62.9–95.4], P = 0.01; 2‐year LFS FB2A2: 38% [16–59.9] vs. CloB2A2: 70.8% [52.6–89], P = 0.03). The better survivals were due to the lower risk of relapse in this CloB2A2 AML subgroup (2‐year RI FB2A2: 41.2% [19–62.4] vs. CloB2A2: 16.7% [5–34.2], P = 0.05). This retrospective comparison suggests that the CloB2A2 RIC regimen can likely provide longer survival than that awarded by a FB2A2 RIC regimen and may become a new standard of care RIC regimen for allotransplanted AML patients. A prospective phase 3 randomized study is warranted. John Wiley and Sons Inc. 2016-10-17 /pmc/articles/PMC5119961/ /pubmed/27748046 http://dx.doi.org/10.1002/cam4.880 Text en © 2016 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Chevallier, Patrice
Labopin, Myriam
de La Tour, Regis Peffault
Lioure, Bruno
Bulabois, Claude‐Eric
Huynh, Anne
Blaise, Didier
Turlure, Pascal
Daguindau, Etienne
Maillard, Natacha
Yakoub‐Agha, Ibrahim
Guillerm, Gaelle
Delage, Jeremy
Contentin, Nathalie
Bay, Jacques‐Olivier
Beckerich, Florence
Bourhis, Jean‐Henri
Detrait, Marie
Vigouroux, Stéphane
François, Sylvie
Legrand, Faezeh
Guillaume, Thierry
Mohty, Mohamad
Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title_full Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title_fullStr Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title_full_unstemmed Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title_short Clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with AML/MDS
title_sort clofarabine versus fludarabine‐based reduced‐intensity conditioning regimen prior to allogeneic transplantation in adults with aml/mds
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119961/
https://www.ncbi.nlm.nih.gov/pubmed/27748046
http://dx.doi.org/10.1002/cam4.880
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