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Pre-existing invasive fungal infection is not a contraindication for allogeneic HSCT for patients with hematologic malignancies : A CIBMTR study

Authors :
Michael Boeckh
Christopher C. Dvorak
Caroline A. Lindemans
Muthalagu Ramanathan
A. A. McLeod
Jeffery J. Auletta
Min Chen
Lynne Strasfeld
Gregory A. Hale
Bipin N. Savani
Celalettin Ustun
Randy Taplitz
Marcie L. Riches
John R. Wingard
Franklin O. Smith
Rodrigo Martino
Junguee Lee
Eva C. Guinan
Ruta Brazauskas
Hillard M. Lazarus
Vijay Reddy
Richard T. Maziarz
Jane L. Liesveld
M Aljurf
B. Geroge
Minoo Battiwalla
Juan Gea-Banacloche
Source :
Bone marrow transplantation, Bone marrow transplantation, vol 52, iss 2, Bone Marrow Transplantation, 52(2), 270. Nature Publishing Group, BONE MARROW TRANSPLANTATION, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, Instituto de Salud Carlos III (ISCIII)
Publication Year :
2017

Abstract

Patients with prior invasive fungal infection (IFI) increasingly proceed to allogeneic hematopoietic cell transplantation (HSCT). However, little is known about the impact of prior IFI on survival. Patients with pre-transplant IFI (cases; n = 825) were compared with controls (n = 10247). A subset analysis assessed outcomes in leukemia patients pre-and post 2001. Cases were older with lower performance status (KPS), more advanced disease, higher likelihood of AML and having received cord blood, reduced intensity conditioning, mold-active fungal prophylaxis and more recently transplanted. Aspergillus spp. and Candida spp. were the most commonly identified pathogens. 68% of patients had primarily pulmonary involvement. Univariate and multivariable analysis demonstrated inferior PFS and overall survival (OS) for cases. At 2 years, cases had higher mortality and shorter PFS with significant increases in non-relapse mortality (NRM) but no difference in relapse. One year probability of post-HSCT IFI was 24% (cases) and 17% (control, P < 0.001). The predominant cause of death was underlying malignancy; infectious death was higher in cases (13% vs 9%). In the subset analysis, patients transplanted before 2001 had increased NRM with inferior OS and PFS compared with later cases. Pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT but significant survivorship was observed. Consequently, pre-transplant IFI should not be a contraindication to allogeneic HSCT in otherwise suitable candidates. Documented pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT. However, mortality post transplant is more influenced by advanced disease status than previous IFI. Pre-transplant IFI does not appear to be a contraindication to allogeneic HSCT.

Details

Language :
English
ISSN :
02683369
Volume :
52
Issue :
2
Database :
OpenAIRE
Journal :
Bone Marrow Transplantation
Accession number :
edsair.doi.dedup.....4742510b35e02433227b62fd389dddc1