Evidence map›Paper›PMID 33542712›Full record

ArticleFrontiers in immunology2020

Haplotype Motif-Based Models for KIR-Genotype Informed Selection of Hematopoietic Cell Donors Fail to Predict Outcome of Patients With Myelodysplastic Syndromes or Secondary Acute Myeloid Leukemia.

Johannes Schetelig, Henning Baldauf, Linda Koster, Michelle Kuxhausen, Falk Heidenreich, Liesbeth C de Wreede, Stephen Spellman, Michel van Gelder, Benedetto Bruno, Francesco Onida and 12 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  12. DonorFrontiers in immunology · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 15 institutions in 7 countries.

Johannes ScheteligMedizinische Klinik und Poliklinik I, University Hospital Dresden, Dresden, Germany.
Henning BaldaufDKMS Clinical Trials Unit, Dresden, Germany.
Linda KosterEBMT Data Office Leiden, Leiden, Netherlands.
Michelle KuxhausenCenter for International Blood and Marrow Transplant Research, Minneapolis, MN, United States.
Falk HeidenreichMedizinische Klinik und Poliklinik I, University Hospital Dresden, Dresden, Germany.
Liesbeth C de WreedeDKMS Clinical Trials Unit, Dresden, Germany.
Stephen SpellmanCenter for International Blood and Marrow Transplant Research, Minneapolis, MN, United States.
Michel van GelderMaastricht University Medical Center, Department of Internal Medicine, Maastricht, Netherlands.
Benedetto BrunoA.O.U. Citta della Salute e della Scienza di Torino, Turin, Italy.
Francesco OnidaFondazione IRCCS Ca'Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Vinzenz LangeDKMS Life Science Lab, Dresden, Germany.
Carolin MassalskiDKMS Life Science Lab, Dresden, Germany.
Victoria PotterGKT School of Medicine, London, United Kingdom.
Per LjungmanKarolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Nicolaas SchaapRadboud University Medical Centre, Nijmegen, Netherlands.
Patrick HaydenSt. James's Hospital, Dublin, Ireland.
Stephanie J LeeFred Hutchinson Cancer Research Center, Seattle, WA, United States.
Nicolaus KrögerUniversity Hospital Eppendorf, Hamburg, Germany.
Kathy HsuMemorial Sloan Kettering Cancer Center, New York & Scientific Director, CIBMTR Immunobiology Working Committee, New York City, NY, United States.
Alexander H SchmidtDKMS Clinical Trials Unit, Dresden, Germany.
Ibrahim Yakoub-AghaCHU de Lille, LIRIC, INSERM U995, Université de Lille, Lille, France.
Marie RobinHopital Saint-Louis, APHP, Université de Paris, Paris, France.
Deutsche Knochenmarkspenderdatei · DENational Marrow Donor Program · USAssistance Publique – Hôpitaux de Paris · FRAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITEuropean Society for Blood and Marrow Transplantation · NLFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITFred Hutch Cancer Center · USInserm · FRKarolinska University Hospital · SELeiden University Medical Center · NLMaastricht University · NLMemorial Sloan Kettering Cancer Center · USRadboud University Nijmegen · NLSt. James's Hospital · IEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Blood and Marrow Transplant Clinical Trials Network DCC- The Medical College of Wisconsin, Inc.U24HL138660 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI Steven M. DeVine, Mehdi Hussain Hamadani · 2017 to 2026
$71.4M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI FELICES, MARTIN · 2005 to 2025
$38.2M
Hematopopietic Stem Cell TransplantationU01AI069197 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Effie W Petersdorf · 2005 to 2026
$18.9M
Randomized study of low versus moderate dose busulfan in transplant for severe combined immunodeficiencyU01AI126612 · NIAID · CHILDREN'S HOSPITAL OF LOS ANGELES · PI KEAN, LESLIE S, PULSIPHER, MICHAEL A · 2017 to 2023
$8.5M
Immuno and Epigenetics of Hematopoietic Cell TransplantationR01CA218285 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Effie W Petersdorf · 2017 to 2026
$5.6M
The role of TCOF1 in germline predisposition to and in leukemic transformation of chronic myelomonocytic leukemiaR01CA152108 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Jing Zhang · 2011 to 2026
$5.4M
Integrated Exchange and Storage of Current- and Future-Generation Immunogenomic DataR01AI128775 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JILL Allison HOLLENBACH, STEVEN JOHN MACK · 2017 to 2026
$4.5M
Identifying Predictors of Poor Health-Related Quality-of-life among Pediatric Hematopoietic Stem Cell DonorsR01HL131731 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PULSIPHER, MICHAEL A, SWITZER, GALEN E. · 2018 to 2022
$3.6M
Integrating health informatics in a scalable stepped care self-management program for survivors after hematopoietic cell transplantationR01CA215134 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BAKER, KEVIN S, MAJHAIL, NAVNEET S. · 2017 to 2022
$3.6M
Selection of Allogeneic Hematopoietic Cell Donor Based on KIR and HLA GenotypesR01HL129472 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI HSU, KATHARINE C · 2015 to 2019
$2.6M
NCI NIH HHS P01 CA111412NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA152108NCI NIH HHS R01 CA215134NCI NIH HHS R01 CA218285NCI NIH HHS R01 CA231141NCI NIH HHS U24 CA076518NHLBI NIH HHS R01 HL126589NHLBI NIH HHS R01 HL129472NHLBI NIH HHS R01 HL130388NHLBI NIH HHS R01 HL131731NHLBI NIH HHS R21 HL140314NHLBI NIH HHS U01 HL128568NHLBI NIH HHS U24 HL138660NIAID NIH HHS R01 AI128775NIAID NIH HHS U01 AI069197NIAID NIH HHS U01 AI126612
6 · The paper itself

Abstract

Results from registry studies suggest that harnessing Natural Killer (NK) cell reactivity mediated through Killer cell Immunoglobulin-like Receptors (KIR) could reduce the risk of relapse after allogeneic Hematopoietic Cell Transplantation (HCT). Several competing models have been developed to classify donors as KIR-advantageous or disadvantageous. Basically, these models differ by grouping donors based on distinct KIR-KIR-ligand combinations or by haplotype motif assignment. This study aimed to validate different models for unrelated donor selection for patients with Myelodysplatic Syndromes (MDS) or secondary Acute Myeloid Leukemia (sAML). In a joint retrospective study of the European Society for Blood and Marrow Transplantation (EBMT) and the Center for International Blood and Marrow Transplant Research (CIBMTR) registry data from 1704 patients with secondary AML or MDS were analysed. The cohort consisted mainly of older patients (median age 61 years) with high risk disease who had received chemotherapy-based reduced intensity conditioning and anti-thymocyte globulin prior to allogeneic HCT from well-matched unrelated stem cell donors. The impact of the predictors on Overall Survival (OS) and relapse incidence was tested in Cox regression models adjusted for patient age, a modified disease risk index, performance status, donor age, HLA-match, sex-match, CMV-match, conditioning intensity, type of T-cell depletion and graft type.

Indexed as

AdolescentAdultAgedAged, 80 and overDonor SelectionFemaleGenotypeGraft vs Host DiseaseHaplotypesHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesReceptors, KIRReceptors, KIRdonor selectionhematopoietic stem cell transplantationKIRKIR2DS1KIR3DL1unrelated donor

Identifiers

PMID33542712
PMCPMC7851088
OpenAlexW3122354936

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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.