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HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors

Even if the overall survival of children with cancer is significantly improved over these decades, the cure rate of high-risk pediatric solid tumors such as neuroblastoma, Ewing's sarcoma family tumors or rhabdomiosarcoma remain challenging. Autologous hematopoietic stem cell transplantation (H...

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Autores principales: Pession, Andrea, Masetti, Riccardo, Di Leo, Corinne, Franzoni, Monica, Prete, Arcangelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206527/
https://www.ncbi.nlm.nih.gov/pubmed/22053274
http://dx.doi.org/10.4081/pr.2011.s2.e12
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author Pession, Andrea
Masetti, Riccardo
Di Leo, Corinne
Franzoni, Monica
Prete, Arcangelo
author_facet Pession, Andrea
Masetti, Riccardo
Di Leo, Corinne
Franzoni, Monica
Prete, Arcangelo
author_sort Pession, Andrea
collection PubMed
description Even if the overall survival of children with cancer is significantly improved over these decades, the cure rate of high-risk pediatric solid tumors such as neuroblastoma, Ewing's sarcoma family tumors or rhabdomiosarcoma remain challenging. Autologous hematopoietic stem cell transplantation (HSCT) allows chemotherapy dose intensification beyond marrow tolerance and has become a fundamental tool in the multimodal therapeutical approach of these patients. Anyway this procedure does not allow to these children an event-free survival approaching more than 50% at 5 years. New concepts of allogeneic HSCT and in particular HLA-mismatched HSCT for high risk solid tumors do not rely on escalation of chemotherapy intensity and tumor load reduction but rather on a graft-versus-tumor effect. We here report an experimental study design of HLA-mismatched HSCT for the treatment of pediatric solid tumors and the inherent preliminary results.
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spelling pubmed-32065272011-11-03 HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors Pession, Andrea Masetti, Riccardo Di Leo, Corinne Franzoni, Monica Prete, Arcangelo Pediatr Rep Article Even if the overall survival of children with cancer is significantly improved over these decades, the cure rate of high-risk pediatric solid tumors such as neuroblastoma, Ewing's sarcoma family tumors or rhabdomiosarcoma remain challenging. Autologous hematopoietic stem cell transplantation (HSCT) allows chemotherapy dose intensification beyond marrow tolerance and has become a fundamental tool in the multimodal therapeutical approach of these patients. Anyway this procedure does not allow to these children an event-free survival approaching more than 50% at 5 years. New concepts of allogeneic HSCT and in particular HLA-mismatched HSCT for high risk solid tumors do not rely on escalation of chemotherapy intensity and tumor load reduction but rather on a graft-versus-tumor effect. We here report an experimental study design of HLA-mismatched HSCT for the treatment of pediatric solid tumors and the inherent preliminary results. PAGEPress Publications 2011-06-22 /pmc/articles/PMC3206527/ /pubmed/22053274 http://dx.doi.org/10.4081/pr.2011.s2.e12 Text en ©Copyright A. Pession et al., 2011 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BYNC 3.0). Licensee PAGEPress, Italy
spellingShingle Article
Pession, Andrea
Masetti, Riccardo
Di Leo, Corinne
Franzoni, Monica
Prete, Arcangelo
HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title_full HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title_fullStr HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title_full_unstemmed HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title_short HLA-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
title_sort hla-mismatched hematopoietic stem cell tranplantation for pediatric solid tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3206527/
https://www.ncbi.nlm.nih.gov/pubmed/22053274
http://dx.doi.org/10.4081/pr.2011.s2.e12
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