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Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France

Allogeneic stem cell transplantation remains the only curative treatment for sickle cell anemia (SCA), but the place of myeloablative conditioning in the procedure remains to be defined. The aim of the present study was to analyze long-term outcomes, including chimerism, SCA-related events and biolo...

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Autores principales: Bernaudin, Françoise, Dalle, Jean-Hugues, Bories, Dominique, de Latour, Regis Peffault, Robin, Marie, Bertrand, Yves, Pondarre, Corinne, Vannier, Jean-Pierre, Neven, Benedicte, Kuentz, Mathieu, Maury, Sébastien, Lutz, Patrick, Paillard, Catherine, Yakouben, Karima, Thuret, Isabelle, Galambrun, Claire, Dhedin, Nathalie, Jubert, Charlotte, Rohrlich, Pierre, Bay, Jacques-Olivier, Suarez, Felipe, Raus, Nicole, Vernant, Jean-Paul, Gluckman, Eliane, Poirot, Catherine, Socié, Gérard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939536/
https://www.ncbi.nlm.nih.gov/pubmed/31097628
http://dx.doi.org/10.3324/haematol.2018.213207
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author Bernaudin, Françoise
Dalle, Jean-Hugues
Bories, Dominique
de Latour, Regis Peffault
Robin, Marie
Bertrand, Yves
Pondarre, Corinne
Vannier, Jean-Pierre
Neven, Benedicte
Kuentz, Mathieu
Maury, Sébastien
Lutz, Patrick
Paillard, Catherine
Yakouben, Karima
Thuret, Isabelle
Galambrun, Claire
Dhedin, Nathalie
Jubert, Charlotte
Rohrlich, Pierre
Bay, Jacques-Olivier
Suarez, Felipe
Raus, Nicole
Vernant, Jean-Paul
Gluckman, Eliane
Poirot, Catherine
Socié, Gérard
author_facet Bernaudin, Françoise
Dalle, Jean-Hugues
Bories, Dominique
de Latour, Regis Peffault
Robin, Marie
Bertrand, Yves
Pondarre, Corinne
Vannier, Jean-Pierre
Neven, Benedicte
Kuentz, Mathieu
Maury, Sébastien
Lutz, Patrick
Paillard, Catherine
Yakouben, Karima
Thuret, Isabelle
Galambrun, Claire
Dhedin, Nathalie
Jubert, Charlotte
Rohrlich, Pierre
Bay, Jacques-Olivier
Suarez, Felipe
Raus, Nicole
Vernant, Jean-Paul
Gluckman, Eliane
Poirot, Catherine
Socié, Gérard
author_sort Bernaudin, Françoise
collection PubMed
description Allogeneic stem cell transplantation remains the only curative treatment for sickle cell anemia (SCA), but the place of myeloablative conditioning in the procedure remains to be defined. The aim of the present study was to analyze long-term outcomes, including chimerism, SCA-related events and biological data (hemoglobin, reticulocytes, HbS%), and fertility in a French series of 234 SCA patients under 30 years of age who, from 1988 to 2012, received a matched-sibling-donor stem cell transplantation following standardized myeloablative conditioning [busulfan, cyclophosphamide and rabbit antithymocyte globulin (ATG)]. Since the first report of the series (1988-2004), 151 new consecutive patients with SCA have been similarly transplanted. Considering death, non-engraftment or rejection (donor cells <5%) as events, the 5-year event-free survival was 97.9% (95% confidence interval: 95.5-100%), confirming, since the year 2000, an at least 95% chance of cure. In the overall cohort (n=234, median follow up 7.9 years), event-free survival was not associated with age, but chronic-graft-versus-host disease (cGvHD) was independently associated with recipient’s age >15 years (hazard ratio=4.37; P=0.002) and lower (5-15 vs. 20 mg/kg) ATG dose (hazard ratio=4.55; P=0.001). At one year, 44% of patients had mixed chimerism (5-95% donor cells), but those prepared with ATG had no graft rejection. No events related to SCA occurred in patients with mixed chimerism, even those with 15-20% donor cells, but hemolytic anemia stigmata were observed with donor cells <50%. Myeloablative transplantation with matched-sibling donor currently has a higher event-free survival (98%) in patients under 30 years of age than that reported for non-myeloablative conditioning (88%). Nevertheless, the risk of cGvHD in older patients and the need to preserve fertility might be indications for a non-myeloablative conditioning.
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spelling pubmed-69395362020-01-06 Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France Bernaudin, Françoise Dalle, Jean-Hugues Bories, Dominique de Latour, Regis Peffault Robin, Marie Bertrand, Yves Pondarre, Corinne Vannier, Jean-Pierre Neven, Benedicte Kuentz, Mathieu Maury, Sébastien Lutz, Patrick Paillard, Catherine Yakouben, Karima Thuret, Isabelle Galambrun, Claire Dhedin, Nathalie Jubert, Charlotte Rohrlich, Pierre Bay, Jacques-Olivier Suarez, Felipe Raus, Nicole Vernant, Jean-Paul Gluckman, Eliane Poirot, Catherine Socié, Gérard Haematologica Article Allogeneic stem cell transplantation remains the only curative treatment for sickle cell anemia (SCA), but the place of myeloablative conditioning in the procedure remains to be defined. The aim of the present study was to analyze long-term outcomes, including chimerism, SCA-related events and biological data (hemoglobin, reticulocytes, HbS%), and fertility in a French series of 234 SCA patients under 30 years of age who, from 1988 to 2012, received a matched-sibling-donor stem cell transplantation following standardized myeloablative conditioning [busulfan, cyclophosphamide and rabbit antithymocyte globulin (ATG)]. Since the first report of the series (1988-2004), 151 new consecutive patients with SCA have been similarly transplanted. Considering death, non-engraftment or rejection (donor cells <5%) as events, the 5-year event-free survival was 97.9% (95% confidence interval: 95.5-100%), confirming, since the year 2000, an at least 95% chance of cure. In the overall cohort (n=234, median follow up 7.9 years), event-free survival was not associated with age, but chronic-graft-versus-host disease (cGvHD) was independently associated with recipient’s age >15 years (hazard ratio=4.37; P=0.002) and lower (5-15 vs. 20 mg/kg) ATG dose (hazard ratio=4.55; P=0.001). At one year, 44% of patients had mixed chimerism (5-95% donor cells), but those prepared with ATG had no graft rejection. No events related to SCA occurred in patients with mixed chimerism, even those with 15-20% donor cells, but hemolytic anemia stigmata were observed with donor cells <50%. Myeloablative transplantation with matched-sibling donor currently has a higher event-free survival (98%) in patients under 30 years of age than that reported for non-myeloablative conditioning (88%). Nevertheless, the risk of cGvHD in older patients and the need to preserve fertility might be indications for a non-myeloablative conditioning. Ferrata Storti Foundation 2020-01 /pmc/articles/PMC6939536/ /pubmed/31097628 http://dx.doi.org/10.3324/haematol.2018.213207 Text en Copyright© 2020 Ferrata Storti Foundation Material published in Haematologica is covered by copyright. All rights are reserved to the Ferrata Storti Foundation. Use of published material is allowed under the following terms and conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode. Copies of published material are allowed for personal or internal use. Sharing published material for non-commercial purposes is subject to the following conditions: https://creativecommons.org/licenses/by-nc/4.0/legalcode, sect. 3. Reproducing and sharing published material for commercial purposes is not allowed without permission in writing from the publisher.
spellingShingle Article
Bernaudin, Françoise
Dalle, Jean-Hugues
Bories, Dominique
de Latour, Regis Peffault
Robin, Marie
Bertrand, Yves
Pondarre, Corinne
Vannier, Jean-Pierre
Neven, Benedicte
Kuentz, Mathieu
Maury, Sébastien
Lutz, Patrick
Paillard, Catherine
Yakouben, Karima
Thuret, Isabelle
Galambrun, Claire
Dhedin, Nathalie
Jubert, Charlotte
Rohrlich, Pierre
Bay, Jacques-Olivier
Suarez, Felipe
Raus, Nicole
Vernant, Jean-Paul
Gluckman, Eliane
Poirot, Catherine
Socié, Gérard
Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title_full Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title_fullStr Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title_full_unstemmed Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title_short Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France
title_sort long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in france
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939536/
https://www.ncbi.nlm.nih.gov/pubmed/31097628
http://dx.doi.org/10.3324/haematol.2018.213207
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