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Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC

BACKGROUND: Clofarabine has been proved to have higher anti-leukemic myeloid activity compared to fludarabine, a drug extensively used as part of reduced intensity conditioning (RIC) for allogeneic stem cell transplantation (allo-SCT). RESULTS: Eighty-four patients were included. The majority of pat...

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Autores principales: Le Bourgeois, Amandine, Labopin, Myriam, Leclerc, Mathieu, de Latour, Régis Peffault, Bourhis, Jean-Henri, Ceballos, Patrice, Orvain, Corentin, Wallet, Hélène Labussière, Bilger, Karin, Blaise, Didier, Rubio, Marie-Thérese, Guillaume, Thierry, Mohty, Mohamad, Chevallier, Patrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290956/
https://www.ncbi.nlm.nih.gov/pubmed/30564300
http://dx.doi.org/10.18632/oncotarget.26391
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author Le Bourgeois, Amandine
Labopin, Myriam
Leclerc, Mathieu
de Latour, Régis Peffault
Bourhis, Jean-Henri
Ceballos, Patrice
Orvain, Corentin
Wallet, Hélène Labussière
Bilger, Karin
Blaise, Didier
Rubio, Marie-Thérese
Guillaume, Thierry
Mohty, Mohamad
Chevallier, Patrice
author_facet Le Bourgeois, Amandine
Labopin, Myriam
Leclerc, Mathieu
de Latour, Régis Peffault
Bourhis, Jean-Henri
Ceballos, Patrice
Orvain, Corentin
Wallet, Hélène Labussière
Bilger, Karin
Blaise, Didier
Rubio, Marie-Thérese
Guillaume, Thierry
Mohty, Mohamad
Chevallier, Patrice
author_sort Le Bourgeois, Amandine
collection PubMed
description BACKGROUND: Clofarabine has been proved to have higher anti-leukemic myeloid activity compared to fludarabine, a drug extensively used as part of reduced intensity conditioning (RIC) for allogeneic stem cell transplantation (allo-SCT). RESULTS: Eighty-four patients were included. The majority of patients had acute myeloid leukemia (AML, n = 63). Sixty-one patients were in complete remission (AML n = 55). With a median follow up of 31 months (range: 5.7–74.1), 2-year overall (OS) and disease-free (DFS) survivals, relapse incidence (RI), non-relapse mortality (NRM) and graft-versus-host disease (GVHD)/relapse free survival (GRFS) were 64.5% (53.8–75.2); 57.2% (46.2–68.2); 27.7% (18.2–37.9); 15.1% (8.2–23.9) and 43.6% (32.5–54.7), respectively. Considering AML in remission, 2-year OS, DFS, RI, NRM and GRFS were 74.2% (62–86.5); 66.8% (53.6–79.9); 23.4% (12.7–36); 9.8% (3.5–19.9) and 50.9% (36.9–64.9), respectively. Two-year outcomes were similar between CloB2A1 and CloB2A2 sub-groups. In multivariate analysis, active disease at transplant was the only factor adversely impacting 2 years outcomes. CONCLUSIONS: CloB2A2/A1 RIC regimen provides very good results for AML patients allografted in CR and could be retained as a new RIC platform for these patients. MATERIALS AND METHODS: This was a retrospective study including all patients who received a clofarabine/busulfan based RIC allo-SCT for myeloid malignancies and reported within the SFGM-TC registry. RIC regimen consisted of clofarabine 30 mg/m(2)/day 4 to 5 days (Clo), busulfan 3.2 mg/kg/day 2 days (B2) and 2.5 mg/kg/day of rabbit anti-thymocyte globulin 1 or 2 days (A1 or A2). The primary objective of the study was to report the main outcomes of the whole cohort at 2 years.
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spelling pubmed-62909562018-12-18 Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC Le Bourgeois, Amandine Labopin, Myriam Leclerc, Mathieu de Latour, Régis Peffault Bourhis, Jean-Henri Ceballos, Patrice Orvain, Corentin Wallet, Hélène Labussière Bilger, Karin Blaise, Didier Rubio, Marie-Thérese Guillaume, Thierry Mohty, Mohamad Chevallier, Patrice Oncotarget Research Paper BACKGROUND: Clofarabine has been proved to have higher anti-leukemic myeloid activity compared to fludarabine, a drug extensively used as part of reduced intensity conditioning (RIC) for allogeneic stem cell transplantation (allo-SCT). RESULTS: Eighty-four patients were included. The majority of patients had acute myeloid leukemia (AML, n = 63). Sixty-one patients were in complete remission (AML n = 55). With a median follow up of 31 months (range: 5.7–74.1), 2-year overall (OS) and disease-free (DFS) survivals, relapse incidence (RI), non-relapse mortality (NRM) and graft-versus-host disease (GVHD)/relapse free survival (GRFS) were 64.5% (53.8–75.2); 57.2% (46.2–68.2); 27.7% (18.2–37.9); 15.1% (8.2–23.9) and 43.6% (32.5–54.7), respectively. Considering AML in remission, 2-year OS, DFS, RI, NRM and GRFS were 74.2% (62–86.5); 66.8% (53.6–79.9); 23.4% (12.7–36); 9.8% (3.5–19.9) and 50.9% (36.9–64.9), respectively. Two-year outcomes were similar between CloB2A1 and CloB2A2 sub-groups. In multivariate analysis, active disease at transplant was the only factor adversely impacting 2 years outcomes. CONCLUSIONS: CloB2A2/A1 RIC regimen provides very good results for AML patients allografted in CR and could be retained as a new RIC platform for these patients. MATERIALS AND METHODS: This was a retrospective study including all patients who received a clofarabine/busulfan based RIC allo-SCT for myeloid malignancies and reported within the SFGM-TC registry. RIC regimen consisted of clofarabine 30 mg/m(2)/day 4 to 5 days (Clo), busulfan 3.2 mg/kg/day 2 days (B2) and 2.5 mg/kg/day of rabbit anti-thymocyte globulin 1 or 2 days (A1 or A2). The primary objective of the study was to report the main outcomes of the whole cohort at 2 years. Impact Journals LLC 2018-11-27 /pmc/articles/PMC6290956/ /pubmed/30564300 http://dx.doi.org/10.18632/oncotarget.26391 Text en Copyright: © 2018 Bourgeois et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Le Bourgeois, Amandine
Labopin, Myriam
Leclerc, Mathieu
de Latour, Régis Peffault
Bourhis, Jean-Henri
Ceballos, Patrice
Orvain, Corentin
Wallet, Hélène Labussière
Bilger, Karin
Blaise, Didier
Rubio, Marie-Thérese
Guillaume, Thierry
Mohty, Mohamad
Chevallier, Patrice
Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title_full Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title_fullStr Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title_full_unstemmed Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title_short Clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the SFGM-TC
title_sort clofarabine/busulfan-based reduced intensity conditioning regimens provides very good survivals in acute myeloid leukemia patients in complete remission at transplant: a retrospective study on behalf of the sfgm-tc
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290956/
https://www.ncbi.nlm.nih.gov/pubmed/30564300
http://dx.doi.org/10.18632/oncotarget.26391
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