Allogeneic hematopoietic stem cell transplantation (allo-HSCT) represents the only curative treatment for sickle cell disease (SCD), being successful in around 8590% of patients. Mortality and long-term morbidity (including infertility, gonadal failure, and chronic graft-vs.-host disease) associated with conventional approaches curtail the number of patients who undergo allo-HSCT. Recently, it has been demonstrated that cord blood is as effective as and possibly safer than bone marrow in pediatric patients with SCD. Likewise, transplant strategies based on the use of reduced-intensity regimens and the induction of mixed chimerism have been explored to decrease allo-HSCT short- and long-term complications. Pediatr Blood Cancer 2012;59:372376. (c) 2012 Wiley Periodicals, Inc.

Locatelli, F., Pagliara, D., Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease, <<PEDIATRIC BLOOD & CANCER>>, 2012; 59 (2): 372-376. [doi:10.1002/pbc.24177] [https://hdl.handle.net/10807/245574]

Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease

Locatelli, Franco;
2012

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) represents the only curative treatment for sickle cell disease (SCD), being successful in around 8590% of patients. Mortality and long-term morbidity (including infertility, gonadal failure, and chronic graft-vs.-host disease) associated with conventional approaches curtail the number of patients who undergo allo-HSCT. Recently, it has been demonstrated that cord blood is as effective as and possibly safer than bone marrow in pediatric patients with SCD. Likewise, transplant strategies based on the use of reduced-intensity regimens and the induction of mixed chimerism have been explored to decrease allo-HSCT short- and long-term complications. Pediatr Blood Cancer 2012;59:372376. (c) 2012 Wiley Periodicals, Inc.
2012
Inglese
Locatelli, F., Pagliara, D., Allogeneic hematopoietic stem cell transplantation in children with sickle cell disease, <<PEDIATRIC BLOOD & CANCER>>, 2012; 59 (2): 372-376. [doi:10.1002/pbc.24177] [https://hdl.handle.net/10807/245574]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/245574
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