Evidence map›Paper›PMID 31870931›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2020

A Phase 2 Trial of KIR-Mismatched Unrelated Donor Transplantation Using in Vivo T Cell Depletion with Antithymocyte Globulin in Acute Myelogenous Leukemia: Children's Oncology Group AAML05P1 Study.

Stella M Davies, Robert Iannone, Todd A Alonzo, Yi-Cheng Wang, Robert Gerbing, Sandeep Soni, E Anders Kolb, Soheil Meshinchi, Paul J Orchard, Linda J Burns and 2 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  4. Review
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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

12 authors at 10 institutions in 1 country.

Stella M DaviesDivision of Bone marrow Transplantation and Immune Deficiency, Department of Pediatrics, University of Cincinnati, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio. Electronic address: Stella.Davies@cchmc.org.
Robert IannoneJazz Pharmaceuticals, Philadelphia, Pennsylvania.
Todd A AlonzoChildren's Oncology Group and Department of Preventive Medicine, University of Southern California, Los Angeles, California.
Yi-Cheng WangChildren's Oncology Group, Monrovia, California.
Robert GerbingChildren's Oncology Group, Monrovia, California.
Sandeep SoniPediatrics- Stem Cell Transplant, Lucile Packard Children's Hospital, Stanford University, Palo Alto, California.
E Anders KolbDivision of Pediatric Hematology/Oncology, Alfred I. Dupont Hospital for Children, Wilmington, Delaware.
Soheil MeshinchiDivision of Pediatric Hematology/Oncology, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Paul J OrchardDivision of Pediatric Blood and Marrow Transplantation, University of Minnesota, Minneapolis, Minnesota.
Linda J BurnsNational Marrow Donor Program/Be the Match, Minneapolis, Minnesota.
Shalini ShenoyDivision of Pediatric Hematology/Oncology, Washington University, St Louis, Missouri.
Wing LeungBone Marrow Transplant Department, St Jude Children's Research Hospital, Memphis, Tennessee.
Children's Oncology Group · USAlfred I. duPont Hospital for Children · USCincinnati Children's Hospital Medical Center · USFred Hutch Cancer Center · USJazz Pharmaceuticals (United States) · USNational Marrow Donor Program · USStanford University · USSt. Jude Children's Research Hospital · USUniversity of Minnesota · USWashington University in St. Louis · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Antileukemic effort of NK cells in HCT for pediatric AMLR01CA120583 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI LEUNG, WING · 2007 to 2011
$1.8M
KIR-FAVORABLE HAPLOIDENTICAL TRANSPLANTATION IN CHILDRENR01CA181050 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PULSIPHER, MICHAEL A · 2014 to 2019
$1.8M
NCI NIH HHS R01 CA120583NCI NIH HHS R01 CA181050NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

Patients with acute myelogenous leukemia (AML) who undergo killer immunoglobulin-like receptor (KIR)-mismatched haploidentical hematopoietic stem cell transplantation (HSCT) have improved survival. Children's Oncology Group AAML05P1 is a prospective phase 2 trial of unrelated donor (URD) HSCT in which KIR typing of donors was available to the treating physician at donor selection, aiming to determine feasibility (defined as the ability to obtain donor samples from URDs and obtain KIR data before transplantation) of prospective selection of KIR-mismatched donors and effect on outcomes. Patients age ≤30 years with high-risk AML at presentation or relapsed AML were eligible; the study accrued 90 evaluable patients. After enrollment, as many as 5 potential URD samples were KIR-typed (including gene expression) in a central laboratory and results reported to the treating physician, who made the final donor selection. Cases were categorized as KIR-matched or KIR-mismatched using different published strategies. Overall survival (OS), disease-free survival (DFS), and relapse did not differ significantly by KIR mismatch status. Acute graft-versus-host disease (GVHD) was significantly lower in recipients of KIR-mismatched stem cells (35% versus 60%; P = .027). We examined DFS according to time to natural killer (NK) receptor recovery after HSCT. NK p44 recovery was significantly associated with KIR mismatch and with decreased DFS and increased relapse risk in multivariate Cox analysis (P = .006 and .009, respectively). We show that prospective selection of URD according to KIR type was feasible, acute GVHD was reduced, but survival did not differ using any model of KIR mismatch. However, the study enrolled mostly matched transplants, so ligand-ligand mismatch was rare, and thus the sample size was insufficient to determine potential benefit according to this model. Cord blood recipients demonstrated a trend toward improved DFS with KIR mismatch, but the study was not powered to detect a difference in this small subset of patients. Our data suggest that recovery of NK receptor expression might influence DFS after HSCT.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAdultAntilymphocyte SerumChildHumansProspective StudiesReceptors, KIRT-LymphocytesUnrelated DonorsAntilymphocyte SerumReceptors, KIRAMLKIR matchKIR mismatchPediatric transplantation

Identifiers

PMID31870931
PMCPMC7198330
OpenAlexW2996338616

What OpenQuestion holds

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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.