Evidence map›Paper›PMID 32092137›Full record

ArticleBlood advances2020

KIR B donors improve the outcome for AML patients given reduced intensity conditioning and unrelated donor transplantation.

Daniel Weisdorf, Sarah Cooley, Tao Wang, Elizabeth Trachtenberg, Cynthia Vierra-Green, Stephen Spellman, Jennifer A Sees, Ashley Spahn, Jenny Vogel, Todd A Fehniger and 14 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 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 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Human NK cells and cancer.Oncoimmunology · 2024
    Review
  8. DonorFrontiers in immunology · 2024
    Article
  9. Review
  10. Targeting KIR as a novel approach to improve CAR-NK cell function.Journal of translational genetics and genomics · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Human natural killer cells: Form, function, and development.The Journal of allergy and clinical immunology · 2023
    Review
  15. Review
  16. KIR2DS2 Expression Identifies NK Cells With Enhanced Anticancer Activity.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 13 institutions in 2 countries.

Daniel WeisdorfBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN.
Sarah CooleyBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN.
Tao WangDivision of Biostatistics, Medical College of Wisconsin, Milwaukee, WI.
Elizabeth TrachtenbergDepartment of Structural Biology, Stanford University, Stanford, CA.
Cynthia Vierra-GreenCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Stephen SpellmanCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Jennifer A SeesCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Ashley SpahnCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Jenny VogelCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Todd A FehnigerDivision of Oncology, Department of Medicine, Washington University, St. Louis, MO.
Ann E WoolfreyFred Hutchinson Cancer Research Center, Seattle, WA.
Steven M DevineCenter for International Blood and Marrow Transplant Research, Minneapolis, MN.
Maureen RossRoswell Park Cancer Center, Buffalo, NY.
Edmund K WallerWinship Cancer Institute, Emory University, Atlanta, GA.
Ronald M SobecksCleveland Clinic, Cleveland OH.
Joseph McGuirkKansas University Cancer Center, Kansas City, KS.
Betul OranMD Anderson Cancer Center, Houston, TX.
Sherif S FaragDivision of Hematology and Oncology, Indiana University, Bloomington, IN.
Tsiporah ShoreCornell Weill Medical Center, New York, NY; and.
Koen Van BesienCornell Weill Medical Center, New York, NY; and.
Steven G E MarshAnthony Nolan Research Institute & UCL Cancer Institute, Royal Free Campus, London, United Kingdom.
Lisbeth A GuethleinDepartment of Structural Biology, Stanford University, Stanford, CA.
Peter ParhamDepartment of Structural Biology, Stanford University, Stanford, CA.
Jeffrey S MillerBlood and Marrow Transplant Program, University of Minnesota, Minneapolis, MN.
National Marrow Donor Program · USStanford University · USUniversity of Minnesota · USCornell University · USAnthony Nolan · GBCleveland Clinic · USEmory University · USFred Hutch Cancer Center · USIndiana University Bloomington · USRoswell Park Comprehensive Cancer Center · USThe University of Kansas Cancer Center · USThe University of Texas MD Anderson Cancer Center · USWashington University in St. Louis · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
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
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, JEFFREY S. · 2005 to 2025
$38.2M
Targeting the Bone Marrow Microenvironment In Acute Lymphocytic LeukemiaP50CA171963 · NCI · WASHINGTON UNIVERSITY · PI TODD A FEHNIGER · 2013 to 2026
$31.6M
Immuno-Oncology Translation Network (IOTN): Cellular Immunotherapy Data Resource (CIDR)U24CA233032 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI PASQUINI, MARCELO C. · 2018 to 2019
$9.0M
TRANSLATING NK CELL BIOLOGY INTO CLINICAL CANCER IMMUNOTHERAPYR01CA205239 · NCI · WASHINGTON UNIVERSITY · PI FEHNIGER, TODD A · 2017 to 2020
$2.4M
Hematopoietic Stem Cell Transplantation for Young Adults with SCD - DCCU01HL128568 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI EAPEN, MARY, MENDIZABAL, ADAM M. · 2015 to 2019
$1.7M
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS P30 CA077598NCI NIH HHS P50 CA171963NCI NIH HHS R01 CA205239NCI NIH HHS U24 CA076518NHLBI NIH HHS U01 HL128568NHLBI NIH HHS U24 HL138660
6 · The paper itself

Abstract

Natural killer (NK) cell recognition and killing of target cells are enhanced when inhibitory killer immunoglobulin-like receptors (KIR) are unable to engage their cognate HLA class I ligands. The genes of the KIR locus are organized into either KIR B haplotypes, containing 1 or more activating KIR genes or KIR A haplotypes, which lack those genes. Analysis of unrelated donor (URD) hematopoietic cell transplants (HCT), given to acute myeloid leukemia (AML) patients between 1988 and 2009, showed that KIR B haplotype donors were associated with better outcomes, primarily from relapse protection. Most of these transplants involved marrow grafts, fully myeloablative (MAC) preparative regimens, and significant HLA mismatch. Because the practice of HCT continues to evolve, with increasing use of reduced intensity conditioning (RIC), peripheral blood stem cell grafts, and better HLA match, we evaluated the impact of URD KIR genotype on HCT outcome for AML in the modern era (2010-2016). This analysis combined data from a prospective trial testing URD selection based on KIR genotypes (n = 243) with that from a larger contemporaneous cohort of transplants (n = 2419). We found that KIR B haplotype donors conferred a significantly reduced risk of leukemia relapse and improved disease-free survival after RIC, but not MAC HCT. All genes defining KIR B haplotypes were associated with relapse protection, which was significant only in transplant recipients expressing the C1 epitope of HLA-C. In the context of current HCT practice using RIC, selection of KIR B donors could reduce relapse and improve overall outcome for AML patients receiving an allogeneic HCT.

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteHumansProspective StudiesTransplantation ConditioningUnrelated Donors

Identifiers

PMID32092137
PMCPMC7042994
OpenAlexW3008199892

What OpenQuestion holds

Textmetadata
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.