Evidence map›Paper›PMID 25161269›Full record

ArticleBlood2014

Nonpermissive HLA-DPB1 mismatch increases mortality after myeloablative unrelated allogeneic hematopoietic cell transplantation.

Joseph Pidala, Stephanie J Lee, Kwang Woo Ahn, Stephen Spellman, Hai-Lin Wang, Mahmoud Aljurf, Medhat Askar, Jason Dehn, Marcelo Fernandez Viña, Alois Gratwohl and 19 more

Abstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

154 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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94 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors.

Joseph PidalaH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;
Stephanie J LeeFred Hutchinson Cancer Research Center, Seattle, WA;
Kwang Woo AhnCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Stephen SpellmanCenter for International Blood and Marrow Transplant Research, National Marrow Donor Program, Minneapolis, MN;
Hai-Lin WangCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Mahmoud AljurfKing Faisal Specialist Hospital Center and Research, Riyadh, Saudi Arabia;
Medhat AskarCleveland Clinic Foundation, Cleveland, OH;
Jason DehnNational Marrow Donor Program, Minneapolis, MN;
Marcelo Fernandez ViñaStanford Hospital and Clinics, Stanford, CA;
Alois GratwohlUniversity Hospital Basel, Basel, Switzerland;
Vikas GuptaPrincess Margaret Hospital, Toronto, ON, Canada;
Rabi HannaCleveland Clinic Foundation, Cleveland, OH;
Mary M HorowitzCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Carolyn K HurleyGeorgetown University Hospital, Washington, DC;
Yoshihiro InamotoFred Hutchinson Cancer Research Center, Seattle, WA;
Adetola A KassimVanderbilt University Medical Center, Nashville, TN;
Taiga NishihoriH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;
Carlheinz MuellerZKRD-Zentrales Knochenmarkspender-Register Deutschland, Ulm, Germany;
Machteld OudshoornEuropdonor Foundation, Leiden University Medical Centre, Leiden, The Netherlands;
Effie W PetersdorfFred Hutchinson Cancer Research Center, Seattle, WA;
Vinod PrasadDuke University Medical Center, Durham, NC;
James RobinsonAnthony Nolan Research Institute, Royal Free Hospital, London, United Kingdom; UCL Cancer Institute, University College, London, United Kingdom;
Wael SaberCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI;
Kirk R SchultzBritish Columbia's Children's Hospital, University of British Columbia, Vancouver, BC, Canada;
Bronwen ShawAnthony Nolan Research Institute, Royal Free Hospital, London, United Kingdom; UCL Cancer Institute, University College, London, United Kingdom; Royal Marsden, Sutton, Surrey, United Kingdom;
Jan StorekUniversity of Calgary, Calgary, AB, Canada; and.
William A WoodUniversity of North Carolina Hospitals, Chapel Hill, NC.
Ann E WoolfreyFred Hutchinson Cancer Research Center, Seattle, WA;
Claudio AnasettiH. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;

Funding

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
Clinical Significance of MHC Haplotypes in Hematopoietic Cell TransplantationR01CA100019 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETERSDORF, EFFIE W · 2003 to 2025
$9.1M
NCI NIH HHS R01 CA100019NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

We examined current outcomes of unrelated donor allogeneic hematopoietic cell transplantation (HCT) to determine the clinical implications of donor-recipient HLA matching. Adult and pediatric patients who had first undergone myeloablative-unrelated bone marrow or peripheral blood HCT for acute myelogenous leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, and myelodysplastic syndrome between 1999 and 2011 were included. All had high-resolution typing for HLA-A, -B, -C, and -DRB1. Of the total (n = 8003), cases were 8/8 (n = 5449), 7/8 (n = 2071), or 6/8 (n = 483) matched. HLA mismatch (6-7/8) conferred significantly increased risk for grades II to IV and III to IV acute graft vs host disease (GVHD), chronic GVHD, transplant-related mortality (TRM), and overall mortality compared with HLA-matched cases (8/8). Type (allele/antigen) and locus (HLA-A, -B, -C, and -DRB1) of mismatch were not associated with overall mortality. Among 8/8 matched cases, HLA-DPB1 and -DQB1 mismatch resulted in increased acute GVHD, and HLA-DPB1 mismatch had decreased relapse. Nonpermissive HLA-DPB1 allele mismatch was associated with higher TRM compared with permissive HLA-DPB1 mismatch or HLA-DPB1 match and increased overall mortality compared with permissive HLA-DPB1 mismatch in 8/8 (and 10/10) matched cases. Full matching at HLA-A, -B, -C, and -DRB1 is required for optimal unrelated donor HCT survival, and avoidance of nonpermissive HLA-DPB1 mismatches in otherwise HLA-matched pairs is indicated.

Indexed as

Histocompatibility TestingAdolescentAdultChildFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHistocompatibilityHLA-DP beta-ChainsHumansLeukemiaLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesHLA-DPB1 antigenHLA-DP beta-Chains

Identifiers

PMID25161269
PMCPMC4199961

What OpenQuestion holds

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Read underepoch 390

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.