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

  • R. T. Maziarz
  • , R. Brazauskas
  • , M. Chen
  • , A. A. McLeod
  • , R. Martino
  • , J. R. Wingard
  • , M. Aljurf
  • , M. Battiwalla
  • , C. C. Dvorak
  • , B. Geroge
  • , E. C. Guinan
  • , G. A. Hale
  • , H. M. Lazarus
  • , J. W. Lee
  • , J. L. Liesveld
  • , M. Ramanathan
  • , V. Reddy
  • , B. N. Savani
  • , F. O. Smith
  • , L. Strasfeld
  • R. A. Taplitz, C. Ustun, M. J. Boeckh, J. Gea-Banacloche, C. A. Lindemans, J. J. Auletta, M. L. Riches
  • Oregon Health and Science University
  • Medical College of Wisconsin
  • Hospital de La Santa Creu I Sant Pau
  • University of Florida
  • King Faisal Specialist Hospital and Research Centre
  • National Institutes of Health
  • University of California at San Francisco
  • Christian Medical College
  • Dana-Farber Cancer Institute
  • Johns Hopkins University
  • Case Western Reserve University
  • University of Rochester
  • University of Massachusetts Medical School
  • University of Central Florida
  • Vanderbilt University
  • University of Cincinnati
  • University of California at San Diego
  • Fairview Health Service
  • Fred Hutchinson Cancer Research Center
  • Utrecht University
  • Nationwide Children’s Hospital
  • University of North Carolina at Chapel Hill

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

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.

Original languageEnglish
Pages (from-to)270-278
Number of pages9
JournalBone Marrow Transplantation
Volume52
Issue number2
DOIs
StatePublished - 1 Feb 2017

Bibliographical note

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© 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.

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