Evidence map›Paper›PMID 32203258›Full record

ArticleBone marrow transplantation2020

Presence of donor-encoded centromeric KIR B content increases the risk of infectious mortality in recipients of myeloablative, T-cell deplete, HLA-matched HCT to treat AML.

Will P Bultitude, Jennifer Schellekens, Richard M Szydlo, Chloe Anthias, Sarah A Cooley, Jeffrey S Miller, Daniel J Weisdorf, Bronwen E Shaw, Chrissy H Roberts, Christian A Garcia-Sepulveda and 17 more

Open access · greenAbstract read
In one paragraph

Article in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Following Transplantation for Acute Myelogenous Leukemia, DonorJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  9. 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 16 institutions in 3 countries.

Will P BultitudeAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Jennifer SchellekensAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Richard M SzydloAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Chloe AnthiasAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Sarah A CooleyFate Therapeutics, San Diego, CA, USA.
Jeffrey S MillerHaematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN, USA.
Daniel J WeisdorfHaematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN, USA.
Bronwen E ShawCIBMTR and Froedtert and the Medical College of Wisconsin Clinical Cancer Center, Wisconsin, WI, USA.
Chrissy H RobertsLondon School of Hygiene and Tropical Medicine, London, UK.ORCID http://orcid.org/0000-0003-1064-5980
Christian A Garcia-SepulvedaLaboratorio de Genómica Viral y Humana, Facultad de Medicina, Universidad Autónoma de San Luis Potosi, San Luis Potosi, SLP, Mexico.
Julia LeeBritish Society of Blood and Marrow Transplantation and Cellular Therapy, Guy's Hospital, London, UK.
Rachel M PearceBritish Society of Blood and Marrow Transplantation and Cellular Therapy, Guy's Hospital, London, UK.
Marie C WilsonAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Michael N PotterRoyal Marsden Hospital, Surrey, UK.
Jenny L ByrneNottingham University Hospital, Nottingham, UK.ORCID http://orcid.org/0000-0002-9381-1851
Nigel H RussellNottingham University Hospital, Nottingham, UK.
Stephen MacKinnonUniversity College London Hospitals NHS Foundation Trust, London, UK.
Adrian J BloorThe Christie NHS Foundation Trust, Manchester, UK.
Amit PatelLiverpool University Hospital, Liverpool, UK.ORCID http://orcid.org/0000-0003-0029-4611
I Grant McQuakerWest of Scotland Cancer Centre, Gartnavel General Hospital, Glasgow, UK.
Ram MalladiUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Eleni TholouliManchester University NHS Foundation Trust, Manchester, UK.
Kim OrchardUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Victoria T PotterKings College Hospital, London, UK.
J Alejandro MadrigalAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Neema P MayorAnthony Nolan Research Institute, Royal Free Hospital, London, UK.
Steven G E MarshAnthony Nolan Research Institute, Royal Free Hospital, London, UK. steven.marsh@ucl.ac.uk.
Anthony Nolan · GBGuy's Hospital · GBUniversity of Minnesota · USAutonomous University of San Luis Potosí · MXFate Therapeutics (United States) · USFroedtert Hospital · USGartnavel General Hospital · GBKing's College Hospital · GBLondon School of Hygiene & Tropical Medicine · GBManchester University NHS Foundation Trust · GBRoyal Marsden Hospital · GBThe Christie NHS Foundation Trust · GBUniversity College London Hospitals NHS Foundation Trust · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Liverpool · GB

Funding

Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI FELICES, MARTIN · 2005 to 2025
$38.2M
NCI NIH HHS P01 CA111412
6 · The paper itself

Abstract

The reported influence of donor Killer-cell Immunoglobulin-like Receptor (KIR) genes on the outcomes of haematopoietic cell transplantation (HCT) are contradictory, in part due to diversity of disease, donor sources, era and conditioning regimens within and between different studies. Here, we describe the results of a retrospective clinical analysis establishing the effect of donor KIR motifs on the outcomes of 119 HLA-matched, unrelated donor HCT for adult acute myeloid leukaemia (AML) using myeloablative conditioning (MAC) in a predominantly T-cell deplete (TCD) cohort. We observed that HCT involving donors with at least one KIR B haplotype were more likely to result in non-relapse mortality (NRM) than HCT involving donors with two KIR A haplotypes (p = 0.019). Upon separation of KIR haplotypes into their centromeric (Cen) and telomeric (Tel) motif structures, we demonstrated that the Cen-B motif was largely responsible for this effect (p = 0.001). When the cause of NRM was investigated further, infection was the dominant cause of death (p = 0.006). No evidence correlating donor KIR B haplotype with relapse risk was observed. The results from this analysis confirm previous findings in the unrelated, TCD, MAC transplant setting and imply a protective role for donor-encoded Cen-A motifs against infection in allogeneic HCT recipients.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteReceptors, KIRAdultHLA AntigensHumansNeoplasm Recurrence, LocalRetrospective StudiesT-LymphocytesHLA AntigensReceptors, KIR

Identifiers

PMID32203258
PMCPMC8852820
OpenAlexW3010722323

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.