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Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation

In all, 661 of 680 centers in 48 countries reported 37 818 hematopoietic SCT (HSCT) in 33 678 patients (14 165 allogeneic (42%), 19 513 autologous (58%)) in the 2012 survey. Main indications were leukemias, 10 641 (32% 95% allogeneic); lymphoid neoplasias, 19 336 (57% 11% allogeneic); solid tumors,...

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Autores principales: Passweg, J R, Baldomero, H, Peters, C, Gaspar, H B, Cesaro, S, Dreger, P, Duarte, R F, Falkenburg, J H F, Farge-Bancel, D, Gennery, A, Halter, J, Kröger, N, Lanza, F, Marsh, J, Mohty, M, Sureda, A, Velardi, A, Madrigal, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051369/
https://www.ncbi.nlm.nih.gov/pubmed/24637898
http://dx.doi.org/10.1038/bmt.2014.55
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author Passweg, J R
Baldomero, H
Peters, C
Gaspar, H B
Cesaro, S
Dreger, P
Duarte, R F
Falkenburg, J H F
Farge-Bancel, D
Gennery, A
Halter, J
Kröger, N
Lanza, F
Marsh, J
Mohty, M
Sureda, A
Velardi, A
Madrigal, A
author_facet Passweg, J R
Baldomero, H
Peters, C
Gaspar, H B
Cesaro, S
Dreger, P
Duarte, R F
Falkenburg, J H F
Farge-Bancel, D
Gennery, A
Halter, J
Kröger, N
Lanza, F
Marsh, J
Mohty, M
Sureda, A
Velardi, A
Madrigal, A
author_sort Passweg, J R
collection PubMed
description In all, 661 of 680 centers in 48 countries reported 37 818 hematopoietic SCT (HSCT) in 33 678 patients (14 165 allogeneic (42%), 19 513 autologous (58%)) in the 2012 survey. Main indications were leukemias, 10 641 (32% 95% allogeneic); lymphoid neoplasias, 19 336 (57% 11% allogeneic); solid tumors, 1630 (5% 3% allogeneic); and nonmalignant disorders, 1953 (6% 90% allogeneic). There were more unrelated donors than HLA-identical sibling donors (54% versus 38% (8% being mismatched related donor HSCT)). Cord blood was almost exclusive in allogeneic transplants (5% of total). Since 2011, the highest increases in allogeneic HSCT were for AML in CR1 (12%) and for myeloproliferative neoplasm (15%). For autologous HSCT the main increases were for plasma cell disorders (7%), non-Hodgkin lymphoma (4%) and autoimmune disease (50%). There were 4097 pediatric patients <18 years of age receiving HSCT, 2902 received an allogeneic and 1195 an autologous HSCT. Overall, 69% of allogeneic and 64% of autologous HSCT were performed in dedicated pediatric centers and the remainder in combined adult and pediatric centers. Distributions of diseases, donor types and stem cell source for all patients and pediatric patients in particular are shown. A percentage of centers fulfilling the annual required criteria for patient numbers for JACIE accreditation are provided.
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spelling pubmed-40513692014-06-13 Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation Passweg, J R Baldomero, H Peters, C Gaspar, H B Cesaro, S Dreger, P Duarte, R F Falkenburg, J H F Farge-Bancel, D Gennery, A Halter, J Kröger, N Lanza, F Marsh, J Mohty, M Sureda, A Velardi, A Madrigal, A Bone Marrow Transplant Original Article In all, 661 of 680 centers in 48 countries reported 37 818 hematopoietic SCT (HSCT) in 33 678 patients (14 165 allogeneic (42%), 19 513 autologous (58%)) in the 2012 survey. Main indications were leukemias, 10 641 (32% 95% allogeneic); lymphoid neoplasias, 19 336 (57% 11% allogeneic); solid tumors, 1630 (5% 3% allogeneic); and nonmalignant disorders, 1953 (6% 90% allogeneic). There were more unrelated donors than HLA-identical sibling donors (54% versus 38% (8% being mismatched related donor HSCT)). Cord blood was almost exclusive in allogeneic transplants (5% of total). Since 2011, the highest increases in allogeneic HSCT were for AML in CR1 (12%) and for myeloproliferative neoplasm (15%). For autologous HSCT the main increases were for plasma cell disorders (7%), non-Hodgkin lymphoma (4%) and autoimmune disease (50%). There were 4097 pediatric patients <18 years of age receiving HSCT, 2902 received an allogeneic and 1195 an autologous HSCT. Overall, 69% of allogeneic and 64% of autologous HSCT were performed in dedicated pediatric centers and the remainder in combined adult and pediatric centers. Distributions of diseases, donor types and stem cell source for all patients and pediatric patients in particular are shown. A percentage of centers fulfilling the annual required criteria for patient numbers for JACIE accreditation are provided. Nature Publishing Group 2014-06 2014-03-17 /pmc/articles/PMC4051369/ /pubmed/24637898 http://dx.doi.org/10.1038/bmt.2014.55 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Passweg, J R
Baldomero, H
Peters, C
Gaspar, H B
Cesaro, S
Dreger, P
Duarte, R F
Falkenburg, J H F
Farge-Bancel, D
Gennery, A
Halter, J
Kröger, N
Lanza, F
Marsh, J
Mohty, M
Sureda, A
Velardi, A
Madrigal, A
Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title_full Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title_fullStr Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title_full_unstemmed Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title_short Hematopoietic SCT in Europe: data and trends in 2012 with special consideration of pediatric transplantation
title_sort hematopoietic sct in europe: data and trends in 2012 with special consideration of pediatric transplantation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051369/
https://www.ncbi.nlm.nih.gov/pubmed/24637898
http://dx.doi.org/10.1038/bmt.2014.55
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