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Leuk Res. 2013;37(10):1241-7.

Hepatic sinusoidal obstruction syndrome after allogeneic hematopoietic stem cell transplantation in adult patients with idiopathic aplastic anemia.

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교신저자 윤성수

소속 (1)
  1. Divison of Hematology and Hematological Malignancies, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.

Abstract

We retrospectively investigated the incidence, risk factors, and outcomes of SOS (sinusoidal obstruction syndrome; previously veno-occlusive disease [VOD]) after allogeneic hematopoietic stem cell transplantation (alloHSCT) in aplastic anemia. Two hundred and sixty patients were included in the analysis. SOS developed in 7.3% (n=19/260) of patients. Classical Cy (200 mg/m(2))-ATG was the most common conditioning regimen (84.2%) in the SOS group. The SOS mortality rate was 4/19 (21.1%). Univariate analyses revealed that Cy 200 mg/m(2) conditioning (p=0.035), classical Cy-ATG conditioning (p=0.007), and horse ATG conditioning (p<0.001) were significant risk factors for developing SOS. Multivariate analysis revealed that only horse ATG conditioning was a poor prognostic factor (HR=3.484; 95% CI 1.226-9.904; p=0.002). Rabbit ATG (HR 12.719; 95% CI 2.332-69.373; p=0.003) and weight gain>10% (HR 35.655; 95% CI 2.208-575.805; p=0.012) were risk factors in the overall SOS group. Both rabbit ATG conditioning and weight gain of more than 10% were associated with poor overall survival with a median of 1.2 months (5Y survival rate, any risk factor vs. none: 74.6% vs. 0.0%; p<0.001; Fig. 2) in the SOS group. In conclusion, SOS is a relatively rare (7.3%) but highly fatal (21.1%) acute complication of alloHSCT in AA, and the horse ATG conditioning regimen was a significant risk factor for developing SOS.

Copyright © 2013 Elsevier Ltd. All rights reserved.

Keywords

Allogeneic hematopoietic stem cell transplantationAplastic anemiaSinusoidal obstruction syndromeVeno-occlusive disease

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Leukemia research · eISSN 1873-5835
전자 출판
2013-07-18
MeSH
Adolescent · Adult · Anemia, Aplastic / complications / mortality / therapy · Female · Hematopoietic Stem Cell Transplantation* / adverse effects · Hepatic Veno-Occlusive Disease / etiology / mortality / prevention & control / therapy · Humans · Male · Middle Aged · Prognosis · Retrospective Studies · Risk Factors · Transplantation Conditioning · Transplantation, Homologous · Young Adult