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Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy

Relapsed/refractory acute lymphoblastic leukemia (ALL) is a leading cause of death by cancer in children. Our institution has switched relapse treatment strategy to improve survival. We reviewed records of first relapse/refractory childhood ALL between 1996 and 2012. Based on length of first remissi...

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Autores principales: Ceppi, Francesco, Duval, Michel, Leclerc, Jean-Marie, Laverdiere, Caroline, Delva, Yves-Line, Cellot, Sonia, Teira, Pierre, Bittencourt, Henrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025146/
https://www.ncbi.nlm.nih.gov/pubmed/27632202
http://dx.doi.org/10.1371/journal.pone.0160310
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author Ceppi, Francesco
Duval, Michel
Leclerc, Jean-Marie
Laverdiere, Caroline
Delva, Yves-Line
Cellot, Sonia
Teira, Pierre
Bittencourt, Henrique
author_facet Ceppi, Francesco
Duval, Michel
Leclerc, Jean-Marie
Laverdiere, Caroline
Delva, Yves-Line
Cellot, Sonia
Teira, Pierre
Bittencourt, Henrique
author_sort Ceppi, Francesco
collection PubMed
description Relapsed/refractory acute lymphoblastic leukemia (ALL) is a leading cause of death by cancer in children. Our institution has switched relapse treatment strategy to improve survival. We reviewed records of first relapse/refractory childhood ALL between 1996 and 2012. Based on length of first remission, relapse site and immunophenotype, patients were classified into two groups: standard-risk relapse (SRR) and high-risk relapse and refractory (HRRR). Before 2007, all patients were uniformly treated with the same induction as at presentation, followed by hematopoietic stem cell transplantation (HSCT). Since 2007, treatment was given according to risk of failure: SRR were mostly treated with chemotherapy; HRRR patients underwent HSCT after intensive chemotherapy, aiming reduction of pre-transplant disease burden. Sixty-four patients were included. Thirty (47%) were SRR and 34 (53%) HRRR, including 11 with refractory ALL. Five-years overall survival (OS) and event-free survival (EFS) were similar for SRR, but were significantly higher with new risk-based strategy for HRRR: 56% versus 17% (P = 0.03) for OS, and 56% vs 11% for EFS (P = 0.008), respectively. In multivariate analysis, treatment strategy was significantly associated with survival. In conclusion, change for a risk-based strategy in our institution increased survival of high-risk patients to levels similar of those of standard-risk patients.
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spelling pubmed-50251462016-09-27 Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy Ceppi, Francesco Duval, Michel Leclerc, Jean-Marie Laverdiere, Caroline Delva, Yves-Line Cellot, Sonia Teira, Pierre Bittencourt, Henrique PLoS One Research Article Relapsed/refractory acute lymphoblastic leukemia (ALL) is a leading cause of death by cancer in children. Our institution has switched relapse treatment strategy to improve survival. We reviewed records of first relapse/refractory childhood ALL between 1996 and 2012. Based on length of first remission, relapse site and immunophenotype, patients were classified into two groups: standard-risk relapse (SRR) and high-risk relapse and refractory (HRRR). Before 2007, all patients were uniformly treated with the same induction as at presentation, followed by hematopoietic stem cell transplantation (HSCT). Since 2007, treatment was given according to risk of failure: SRR were mostly treated with chemotherapy; HRRR patients underwent HSCT after intensive chemotherapy, aiming reduction of pre-transplant disease burden. Sixty-four patients were included. Thirty (47%) were SRR and 34 (53%) HRRR, including 11 with refractory ALL. Five-years overall survival (OS) and event-free survival (EFS) were similar for SRR, but were significantly higher with new risk-based strategy for HRRR: 56% versus 17% (P = 0.03) for OS, and 56% vs 11% for EFS (P = 0.008), respectively. In multivariate analysis, treatment strategy was significantly associated with survival. In conclusion, change for a risk-based strategy in our institution increased survival of high-risk patients to levels similar of those of standard-risk patients. Public Library of Science 2016-09-15 /pmc/articles/PMC5025146/ /pubmed/27632202 http://dx.doi.org/10.1371/journal.pone.0160310 Text en © 2016 Ceppi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ceppi, Francesco
Duval, Michel
Leclerc, Jean-Marie
Laverdiere, Caroline
Delva, Yves-Line
Cellot, Sonia
Teira, Pierre
Bittencourt, Henrique
Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title_full Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title_fullStr Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title_full_unstemmed Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title_short Improvement of the Outcome of Relapsed or Refractory Acute Lymphoblastic Leukemia in Children Using a Risk-Based Treatment Strategy
title_sort improvement of the outcome of relapsed or refractory acute lymphoblastic leukemia in children using a risk-based treatment strategy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025146/
https://www.ncbi.nlm.nih.gov/pubmed/27632202
http://dx.doi.org/10.1371/journal.pone.0160310
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