Volume 21, Issue 6 e12997
ORIGINAL ARTICLE

Allogeneic hematopoietic stem cell transplantation in congenital disorders: A single-center experience

Maura Faraci

Corresponding Author

Maura Faraci

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

Correspondence

Maura Faraci, Stem Cell Transplantation Unit, Department of Haematology/Oncology, Istituto G. Gaslini, Genoa, Italy.

Email: [email protected]

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Stefano Giardino

Stefano Giardino

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

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Francesca Bagnasco

Francesca Bagnasco

Epidemiology, Biostatistics and Committees Unit, Istituto Giannina Gaslini, Genoa, Italy

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Giuseppe Morreale

Giuseppe Morreale

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

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M. Paola Terranova

M. Paola Terranova

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

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Daniela Di Martino

Daniela Di Martino

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

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Edoardo Lanino

Edoardo Lanino

Hematopoietic Stem Cell Transplantation Unit, Paediatric Haematology-Oncology Department, Istituto Giannina Gaslini, Genoa, Italy

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First published: 26 June 2017
Citations: 3

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the treatment of choice for a variety of congenital disorders. We report the experience of children affected by congenital diseases other than bone marrow failure syndromes who received allo-HSCT over a period of 25 years at G. Gaslini Paediatric Research Institute. HSCTs were performed in 57 children with congenital diseases (25 with congenital immunodeficiencies, 10 with severe combined immunodeficiencies, and 22 with metabolic diseases). Overall survival rate at 3 years in the whole group of patients was 76.9%, with a trend in favor of better outcome in children with metabolic diseases and in those who received cord blood cells (85.9%) vs bone marrow cells (72.4%).

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