Evidence map›Paper›PMID 31043425›Full record

ArticleBlood2019

Benefits and challenges with diagnosing chronic and late acute GVHD in children using the NIH consensus criteria.

Geoffrey D E Cuvelier, Eneida R Nemecek, Justin T Wahlstrom, Carrie L Kitko, Victor A Lewis, Tal Schechter, David A Jacobsohn, Andrew C Harris, Michael A Pulsipher, Henrique Bittencourt and 21 more

Registry-linked trialAbstract read
In one paragraph

Article in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04372524 (Biomarker Verification in Pediatric Chronic Graft-Versus-Host Disease), which is not on this map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 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.

NCT04372524 unknown statusnot on this mapstarted 2020, after this paper: background citation

Biomarker Verification in Pediatric Chronic Graft-Versus-Host Disease: Applied Biomarkers to Minimize Long Term Effects of Childhood/Adolescent Cancer Treatment (ABLE) / Pediatric Transplantation & Cellular Therapy Consortium (PTCTC)

TypeobservationalSponsorUniversity of British ColumbiaRan2020 to 2025Enrolled350ConditionsChronic Graft-versus-Host-Disease, Leukemia, Allogeneic Hematopoietic Stem Cell Transplantation, Blood Cancer
3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors.

Geoffrey D E CuvelierCancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada.
Eneida R NemecekPediatric Blood and Marrow Transplant, Doernbechter Children's Hospital, Oregon Health and Science University, Portland, OR.
Justin T WahlstromBenioff Children's Hospital, University of California San Francisco, San Francisco, CA.
Carrie L KitkoVanderbilt University Medical Center, Nashville, TN.
Victor A LewisAlberta Children's Hospital, University of Calgary, Calgary, AB, Canada.
Tal SchechterHospital for Sick Children, University of Toronto, Toronto, ON, Canada.
David A JacobsohnChildren's National Health System, Washington, DC.
Andrew C HarrisPrimary Children's Hospital, University of Utah, Salt Lake City, UT.ORCID 0000-0002-4538-8817
Michael A PulsipherChildren's Hospital Los Angeles, Los Angeles, CA.ORCID 0000-0003-3030-8420
Henrique BittencourtSte. Justine University Hospital Center, Montreal, QC, Canada.
Sung Won ChoiC.S. Mott Children's Hospital, Michigan Medicine, Ann Arbor, MI.ORCID 0000-0002-6321-3834
Emi H CaywoodNemours Alfred I. duPont Hospital for Children, Wilmington, DE.
Kimberly A KasowDivision of Pediatric Hematology-Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Monica BhatiaMorgan Stanley Children's Hospital, Columbia University, New York, NY.
Benjamin R OshrineJohns Hopkins All Children's Hospital, St. Petersburg, FL.
Allyson FlowerNew York Medical College, Valhalla, NY.
Sonali ChaudhuryAnn & Robert H. Lurie Children's Hospital, Northwestern University, Chicago, IL.
Donald CoulterUniversity of Nebraska Medical Center, Omaha, NE.
Joseph H ChewningDivision of Pediatric Hematology-Oncology, Children's of Alabama, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-5554-5890
Michael JoyceNemours Children's Specialty Care, Jacksonville, FL.
Süreyya SavaşanChildren's Hospital of Michigan, Detroit, MI.
Anna B PawlowskaCity of Hope, Duarte, CA.
Gail C MegasonUniversity of Mississippi Medical Center, Jackson, MS.
David MitchellMontreal Children's Hospital, Montreal, QC, Canada.
Alexandra C CheervaNorton Children's Hospital, University of Louisville, Louisville, KY.
Anita LawitschkaSt. Anna Children's Hospital, Medical University Vienna, Vienna, Austria.
Lori J WestAlberta Transplant Institute, University of Alberta, Edmonton, AB, Canada.
Bo PanEPICORE Centre, University of Alberta, Edmonton, AB, Canada; and.
Yazid N Al HamarnehEPICORE Centre, University of Alberta, Edmonton, AB, Canada; and.ORCID 0000-0003-3984-3542
Anat HalevyBritish Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Kirk R SchultzBritish Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Pediatric Blood and Marrow Transplant ConsortiumU01HL069254 · NHLBI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI PULSIPHER, MICHAEL A · 2001 to 2010
$2.0M
NCI NIH HHS P30 CA022453NHLBI NIH HHS U01 HL069254
6 · The paper itself

Abstract

Chronic graft-versus-host disease (cGVHD) and late acute graft-versus-host disease (L-aGVHD) are understudied complications of allogeneic hematopoietic stem cell transplantation in children. The National Institutes of Health Consensus Criteria (NIH-CC) were designed to improve the diagnostic accuracy of cGVHD and to better classify graft-versus-host disease (GVHD) syndromes but have not been validated in patients <18 years of age. The objectives of this prospective multi-institution study were to determine: (1) whether the NIH-CC could be used to diagnose pediatric cGVHD and whether the criteria operationalize well in a multi-institution study; (2) the frequency of cGVHD and L-aGVHD in children using the NIH-CC; and (3) the clinical features and risk factors for cGVHD and L-aGVHD using the NIH-CC. Twenty-seven transplant centers enrolled 302 patients <18 years of age before conditioning and prospectively followed them for 1 year posttransplant for development of cGVHD. Centers justified their cGVHD diagnosis according to the NIH-CC using central review and a study adjudication committee. A total of 28.2% of reported cGVHD cases was reclassified, usually as L-aGVHD, following study committee review. Similar incidence of cGVHD and L-aGVHD was found (21% and 24.7%, respectively). The most common organs involved with diagnostic or distinctive manifestations of cGVHD in children include the mouth, skin, eyes, and lungs. Importantly, the 2014 NIH-CC for bronchiolitis obliterans syndrome perform poorly in children. Past acute GVHD and peripheral blood grafts are major risk factors for cGVHD and L-aGVHD, with recipients ≥12 years of age being at risk for cGVHD. Applying the NIH-CC in pediatrics is feasible and reliable; however, further refinement of the criteria specifically for children is needed.

Indexed as

Acute DiseaseAdolescentAge FactorsChildChild, PreschoolChronic DiseaseConsensus Development Conferences, NIH as TopicFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansMalePractice Guidelines as TopicRisk FactorsSeverity of Illness IndexSymptom Assessment

Identifiers

PMID31043425
PMCPMC6911839

What OpenQuestion holds

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Registered trials

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.