Transplantation for Autoimmune Diseases in North and South America: A Report of the Center for International Blood and Marrow Transplant Research


Autoria(s): Pasquini, Marcelo C.; Voltarelli, Julio; Atkins, Harold L.; Hamerschlak, Nelson; Zhong, Xiaobo; Ahn, Kwang Woo; Sullivan, Keith M.; Carrum, George; Andrey, Jeffrey; Bredeson, Christopher N.; Cairo, Mitchell; Gale, Robert Peter; Hahn, Theresa; Storek, Jan; Horowitz, Mary M.; McSweeney, Peter A.; Griffith, Linda M.; Muraro, Paolo A.; Pavletic, Steven Z.; Nash, Richard A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

04/11/2013

04/11/2013

2012

Resumo

Hematopoietic cell transplantation (HCT) is an emerging therapy for patients with severe autoimmune diseases (AID). We report data on 368 patients with AID who underwent HCT in 64 North and South American transplantation centers reported to the Center for International Blood and Marrow Transplant Research between 1996 and 2009. Most of the HCTs involved autologous grafts (n = 339); allogeneic HCT (n = 29) was done mostly in children. The most common indications for HCT were multiple sclerosis, systemic sclerosis, and systemic lupus erythematosus. The median age at transplantation was 38 years for autologous HCT and 25 years for allogeneic HCT. The corresponding times from diagnosis to HCT were 35 months and 24 months. Three-year overall survival after autologous HCT was 86% (95% confidence interval [CI], 81%-91%). Median follow-up of survivors was 31 months (range, 1-144 months). The most common causes of death were AID progression, infections, and organ failure. On multivariate analysis, the risk of death was higher in patients at centers that performed fewer than 5 autologous HCTs (relative risk, 3.5; 95% CI, 1.1-11.1; P = .03) and those that performed 5 to 15 autologous HCTs for AID during the study period (relative risk, 4.2; 95% CI, 1.5-11.7; P = .006) compared with patients at centers that performed more than 15 autologous HCTs for AID during the study period. AID is an emerging indication for HCT in the region. Collaboration of hematologists and other disease specialists with an outcomes database is important to promote optimal patient selection, analysis of the impact of prognostic variables and long-term outcomes, and development of clinical trials. Biol Blood Marrow Transplant 18: 1471-1478 (2012) (C) 2012 Published by Elsevier Inc. on behalf of American Society for Blood and Marrow Transplantation

Public Health Service from the National Cancer Institute, National Heart, Lung and Blood Institute [U24-CA76518]

Public Health Service from the National Cancer Institute, National Heart, Lung and Blood Institute

National Institute of Allergy and Infectious Diseases

National Institute of Allergy and Infectious Diseases

National Heart, Lung and Blood Institute and National Cancer Institute [5U01HL069294]

National Heart, Lung and Blood Institute and National Cancer Institute

Health Resources and Services Administration [HHSH234200637015C]

Health Resources and Services Administration

Office of Naval Research

Office of Naval Research [N00014-06-1-0704, N00014-08-1-0058]

Allos

Allos

Amgen

Amgen

Angioblast

Angioblast

Identificador

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, NEW YORK, v. 18, n. 10, supl. 1, Part 3, pp. 1471-1478, OCT, 2012

1083-8791

http://www.producao.usp.br/handle/BDPI/37813

10.1016/j.bbmt.2012.06.003

http://dx.doi.org/10.1016/j.bbmt.2012.06.003

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

NEW YORK

Relação

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

Direitos

closedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #AUTOLOGOUS TRANSPLANTS #MULTIPLE SCLEROSIS #AUTOIMMUNITY #STEM-CELL TRANSPLANTATION #DOSE IMMUNOSUPPRESSIVE THERAPY #SEVERE SYSTEMIC-SCLEROSIS #PROGRESSIVE MULTIPLE-SCLEROSIS #RHEUMATOID-ARTHRITIS #LUPUS-ERYTHEMATOSUS #HEMATOPOIETIC SCT #EUROPEAN GROUP #PRIME-TIME #CYCLOPHOSPHAMIDE #HEMATOLOGY #IMMUNOLOGY #TRANSPLANTATION
Tipo

article

original article

publishedVersion