Evidence map›Paper›PMID 27220262›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2016

Donor KIR B Genotype Improves Progression-Free Survival of Non-Hodgkin Lymphoma Patients Receiving Unrelated Donor Transplantation.

Veronika Bachanova, Daniel J Weisdorf, Tao Wang, Steven G E Marsh, Elizabeth Trachtenberg, Michael D Haagenson, Stephen R Spellman, Martha Ladner, Lisbeth A Guethlein, Peter Parham and 2 more

Abstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

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

  1. Pooled it
  2. Guideline
  3. Guideline
  4. Trial
  5. Reduced-Intensity Haploidentical Bone Marrow Transplantation with Post-Transplant Cyclophosphamide for Solid Tumors in Pediatric and Young Adult Patients.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Trial
  6. Article
  7. Review
  8. Article
  9. Targeting KIR as a novel approach to improve CAR-NK cell function.Journal of translational genetics and genomics · 2023
    Article
  10. Review
  11. KIR2DS2 Expression Identifies NK Cells With Enhanced Anticancer Activity.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. NK cells for cancer immunotherapy.Nature reviews. Drug discovery · 2020
    Review
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Veronika BachanovaBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota. Electronic address: bach0173@umn.edu.
Daniel J WeisdorfBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
Tao WangDivision of Biostatistics and Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.
Steven G E MarshAnthony Nolan Research Institute, London, United Kingdom.
Elizabeth TrachtenbergCenter for Genetics & Center for Immunology and Vaccine Development, Children's Hospital of Oakland Research Institute, Oakland, California.
Michael D HaagensonCenter for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
Stephen R SpellmanCenter for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
Martha LadnerCenter for Genetics & Center for Immunology and Vaccine Development, Children's Hospital of Oakland Research Institute, Oakland, California.
Lisbeth A GuethleinDepartments of Structural Biology and Microbiology and Immunology, Stanford University, Stanford, California.
Peter ParhamDepartments of Structural Biology and Microbiology and Immunology, Stanford University, Stanford, California.
Jeffrey S MillerBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.
Sarah A CooleyBlood and Marrow Transplant Program, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.

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
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
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
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
NCATS NIH HHS UL1 TR000114NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NCI NIH HHS P30 CA077598NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069294
6 · The paper itself

Abstract

Donor killer immunoglobulin-like receptor (KIR) genotypes are associated with relapse protection and survival after allotransplantation for acute myelogenous leukemia. We examined the possibility of a similar effect in a cohort of 614 non-Hodgkin lymphoma (NHL) patients receiving unrelated donor (URD) T cell-replete marrow or peripheral blood grafts. Sixty-four percent (n = 396) of donor-recipient pairs were 10/10 allele HLA matched and 26% were 9/10 allele matched. Seventy percent of donors had KIR B/x genotype; the others had KIR A/A genotype. NHL patients receiving 10/10 HLA-matched URD grafts with KIR B/x donors experienced significantly lower relapse at 5 years (26%; 95% confidence interval [CI], 21% to 32% versus 37%; 95% CI, 27% to 46%; P = .05) compared with KIR A/A donors, resulting in improved 5-year progression-free survival (PFS) (35%; 95% CI, 26% to 44% versus 22%; 95% CI, 11% to 35%; P = .007). In multivariate analysis, use of KIR B/x donors was associated with significantly reduced relapse risk (relative risk [RR], .63, P = .02) and improved PFS (RR, .71, P = .008). The relapse protection afforded by KIR B/x donors was not observed in HLA-mismatched transplantations and was not specific to any particular KIR-B gene. Selecting 10/10 HLA-matched and KIR B/x donors should benefit patients with NHL receiving URD allogeneic transplantation.

Indexed as

GenotypeAdultAgedBone Marrow TransplantationDisease-Free SurvivalFemaleHematopoietic Stem Cell TransplantationHistocompatibilityHLA AntigensHumansLymphoma, Non-HodgkinMaleMiddle AgedPeripheral Blood Stem Cell TransplantationReceptors, KIRTransplantation ConditioningHLA AntigensReceptors, KIRAllogeneic transplantationGenotypeKiller immunoglobulin-like receptorNatural killer (NK) cellsNon-Hodgkin lymphoma

Identifiers

PMID27220262
PMCPMC4981536

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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.