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Characteristics of Late Fatal Infections after Allogeneic Hematopoietic Cell Transplantation.

Authors :
Norkin M
Shaw BE
Brazauskas R
Tecca HR
Leather HL
Gea-Banacloche J
T Kamble R
DeFilipp Z
Jacobsohn DA
Ringden O
Inamoto Y
A Kasow K
Buchbinder D
Shaw P
Hematti P
Schears R
Badawy SM
Lazarus HM
Bhatt N
Horn B
Chhabra S
M Page K
Hamilton B
Hildebrandt GC
Yared JA
Agrawal V
M Beitinjaneh A
Majhail N
Kindwall-Keller T
Olsson RF
Schoemans H
Gale RP
Ganguly S
A Ahmed I
Schouten HC
L Liesveld J
Khera N
Steinberg A
Shah AJ
Solh M
Marks DI
Rybka W
Aljurf M
Dietz AC
Gergis U
George B
Seo S
Flowers MED
Battiwalla M
Savani BN
Riches ML
Wingard JR
Source :
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation [Biol Blood Marrow Transplant] 2019 Feb; Vol. 25 (2), pp. 362-368. Date of Electronic Publication: 2018 Oct 02.
Publication Year :
2019

Abstract

We analyzed late fatal infections (LFIs) in allogeneic stem cell transplantation (HCT) recipients reported to the Center for International Blood and Marrow Transplant Research. We analyzed the incidence, infection types, and risk factors contributing to LFI in 10,336 adult and 5088 pediatric subjects surviving for ≥2 years after first HCT without relapse. Among 2245 adult and 377 pediatric patients who died, infections were a primary or contributory cause of death in 687 (31%) and 110 (29%), respectively. At 12 years post-HCT, the cumulative incidence of LFIs was 6.4% (95% confidence interval [CI], 5.8% to 7.0%) in adults, compared with 1.8% (95% CI, 1.4% to 2.3%) in pediatric subjects; P < .001). In adults, the 2 most significant risks for developing LFI were increasing age (20 to 39, 40 to 54, and ≥55 years versus 18 to 19 years) with hazard ratios (HRs) of 3.12 (95% CI, 1.33 to 7.32), 3.86 (95% CI, 1.66 to 8.95), and 5.49 (95% CI, 2.32 to 12.99) and a history of chronic graft-versus-host disease GVHD (cGVHD) with ongoing immunosuppression at 2 years post-HCT compared with no history of GVHD with (HR, 3.87; 95% CI, 2.59 to 5.78). In pediatric subjects, the 3 most significant risks for developing LFI were a history of cGVHD with ongoing immunosuppression (HR, 9.49; 95% CI, 4.39 to 20.51) or without ongoing immunosuppression (HR, 2.7; 95% CI, 1.05 to 7.43) at 2 years post-HCT compared with no history of GVHD, diagnosis of inherited abnormalities of erythrocyte function compared with diagnosis of acute myelogenous leukemia (HR, 2.30; 95% CI, 1.19 to 4.42), and age >10 years (HR, 1.92; 95% CI, 1.15 to 3.2). This study emphasizes the importance of continued vigilance for late infections after HCT and institution of support strategies aimed at decreasing the risk of cGVHD.<br /> (Copyright © 2018. Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1523-6536
Volume :
25
Issue :
2
Database :
MEDLINE
Journal :
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
Publication Type :
Academic Journal
Accession number :
30287390
Full Text :
https://doi.org/10.1016/j.bbmt.2018.09.031