Evidence map›Paper›PMID 27991895›Full record

Trial reportBone marrow transplantation2017

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 and 17 more

Open access · bronzeAbstract readClinical TrialComparative StudyMulticenter Study
In one paragraph

Trial report in Bone marrow transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 37 citations in OpenAlex.

  1. Infection-related mortality after hematopoietic stem cell transplantation in a high antimicrobial resistance setting.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
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  14. JMM case reports · 2018
    Article
  15. Infectious disease in hematopoietic stem cell transplantation.Therapeutic advances in infectious disease
    Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 20 institutions in 6 countries.

R T MaziarzAdult Blood and Marrow Stem Cell Transplant Program, Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
R BrazauskasCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
M ChenCIBMTR, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
A A McLeodAdult Blood and Marrow Stem Cell Transplant Program, Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
R MartinoDivision of Clinical Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
J R WingardDivision of Hematology & Oncology, Department of Medicine, University of Florida, Gainesville, FL, USA.
M AljurfDepartment of Oncology, King Faisal Specialist Hospital Center & Research, Riyadh, Saudi Arabia.
M BattiwallaHematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD, USA.
C C DvorakDepartment of Pediatrics, University of California San Francisco Medical Center, San Francisco, CA, USA.
B GerogeDepartment of Hematology, Christian Medical College, Vellore, India.
E C GuinanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
G A HaleDepartment of Hematology/Oncology, All Children's Hospital, St Petersburg, FL, USA.
H M LazarusSeidman Cancer Center, University Hospitals Case Medical Center, Cleveland, OH, USA.
J-W LeeBMT Center, Seoul St Mary's Hospital, The Catholic University of Korea, Seoul, South Korea.
J L LiesveldDepartment of Medicine, University of Rochester Medical Center, Rochester, NY, USA.
M RamanathanDivision of Hematology and Oncology, Department of Medicine, UMass Memorial Medical Center, Worcester, MA, USA.
V ReddyDepartment of Internal Medicine, University of Central Florida College of Medicine, Orlando, FL, USA.
B N SavaniDivision of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
F O SmithUniversity of Cincinnati Cancer Institute, Cincinnati, OH, USA.
L StrasfeldInfectious Disease Clinic, Oregon Health and Science University, Portland, OR, USA.
R A TaplitzInfectious Diseases Program, UC San Diego Health, La Jolla, CA, USA.
C UstunDivision of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical Center, Minneapolis, MN, USA.
M J BoeckhVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
J Gea-BanaclocheExperimental Transplantation and Immunology Branch, National Institutes of Health-National Cancer Institute, Bethesda, MD, USA.
C A LindemansPediatric Blood and Marrow Transplantation Program, University Medical Center Utrecht, Utrecht, Netherlands.
J J AulettaDivisions of Hematology/Oncology, Bone Marrow Transplantation and Infectious Diseases, Nationwide Children's Hospital, Columbus, OH, USA.
M L RichesDivision of Hematology/Oncology, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Oregon Health & Science University · USMedical College of Wisconsin · USChristian Medical College, Vellore · INDana-Farber Cancer Institute · USFred Hutch Cancer Center · USHospital de Sant Pau · ESJohns Hopkins University · USKing Faisal Specialist Hospital & Research Centre · SANational Heart Lung and Blood Institute · USNational Institutes of Health · USNationwide Children's Hospital · USThe Catholic University of Korea Seoul St. Mary's Hospital · KRUC San Diego Health System · USUMass Memorial Health Care · USUniversity Hospitals Cleveland Medical Center · USUniversity Medical Center Utrecht · NLUniversity of California San Francisco Medical Center · USUniversity of Central Florida · USUniversity of Cincinnati · USUniversity of Florida · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
NCI NIH HHS P30 CA016086NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

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.

Indexed as

AspergillosisAspergillusCandidaCandidiasisCord Blood Stem Cell TransplantationHematologic NeoplasmsRegistriesAdolescentAdultAgedAllograftsChildChild, PreschoolDisease-Free SurvivalFemaleHumans

Identifiers

PMID27991895
PMCPMC5358320
OpenAlexW2564729921

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.