Evidence map›Paper›PMID 39701289›Full record

ArticleTransplantation and cellular therapy2025

Pediatric Transplant and Cellular Therapy Consortium RESILIENT Conference on Pediatric Chronic Graft-Versus-Host Disease Survivorship After Hematopoietic Cell Transplantation: Part I. Phases of Chronic GVHD, Supportive Care, and Systemic Therapy Discontinuation.

Neel S Bhatt, Andrew C Harris, Lev Gorfinkel, Katarzyna Ibanez, Eric R Tkaczyk, Sandra A Mitchell, Stacey Albuquerque, Tal Schechter, Steven Pavletic, Christine N Duncan and 4 more

Abstract read
In one paragraph

Article in Transplantation and cellular therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

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

  1. Guideline
  2. Article
  3. Article
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

14 authors.

Neel S BhattClinical Research Division, Fred Hutchinson Cancer Center; Seattle, Washington.
Andrew C HarrisPediatric Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Center; New York, New York.
Lev GorfinkelDepartment of Pediatric Hematology-Oncology, Boston Children's Hospital, Dana Farber Cancer Institute; Boston, Massachusetts.
Katarzyna IbanezDepartment of Neurology, Rehabilitation Service, Memorial Sloan Kettering Cancer Center; New York, New York.
Eric R TkaczykDepartment of Dermatology, Vanderbilt University Medical Center and Department of Veteran Affairs; Nashville, Tennessee.
Sandra A MitchellOutcomes Research Branch, Division of Cancer Control and Population Sciences, National Cancer Institute; Rockville, Maryland.
Stacey AlbuquerqueBoston Children's Hospital Cancer and Blood Disorders Center, Dana Farber Cancer Institute; Boston, Massachusetts.
Tal SchechterDivision of Pediatric Hematology, Oncology, BMT, and Cellular Therapy, The Hospital for Sick Children, University of Toronto; Toronto, Ontario, Canada.
Steven PavleticCenter for Cancer Research, National Cancer Institute, National Institutes of Health; Bethesda, Maryland.
Christine N DuncanDepartment of Pediatric Hematology-Oncology, Boston Children's Hospital, Dana Farber Cancer Institute; Boston, Massachusetts.
Seth J RotzDivision of Pediatric Hematology, Oncology, and Blood and Marrow Transplantation, Cleveland Clinic; Cleveland, Ohio.
Kirsten WilliamsAflac Blood and Cancer Center, Children's Healthcare of Atlanta, Emory University; Atlanta, Georgia.
Paul A CarpenterClinical Research Division, Fred Hutchinson Cancer Center; Seattle, Washington.
Geoffrey D E CuvelierDepartment of Pediatric Oncology and Transplantation, Alberta Children's Hospital, University of Calgary; Calgary, Alberta, Canada. Electronic address: Geoffrey.cuvelier@albertahealthservices.ca.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Artificial intelligence to estimate extent of cGVHD from patient photosR01HL169944 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Eric R Tkaczyk · 2024 to 2026
$2.3M
Research and Education towards Solutions for Late effects to Innovate, Excel, and Nurture after chronic Graft-versus-Host Disease (RESILIENT after cGVHD)R13HL172559 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI ROTZ, SETH J · 2024 to 2024
$37k
Quantitative assessment of cutaneous systemic sclerosis.I01CX002721 · VA · VETERANS HEALTH ADMINISTRATION · PI TKACZYK, ERIC R · 2024 to 2025
–
GVHD quantitative assessment in skin of Veterans post-HCTIK2CX001785 · VA · VETERANS HEALTH ADMINISTRATION · PI TKACZYK, ERIC R · 2019 to 2024
–
CSRD VA I01 CX002721CSRD VA IK2 CX001785NCI NIH HHS P30 CA008748NHLBI NIH HHS R01 HL169944NHLBI NIH HHS R13 HL172559
6 · The paper itself

Abstract

Current literature lacks details on the impact of pediatric chronic graft-versus-host disease (cGVHD) on long-term survivorship after allogeneic hematopoietic cell transplantation (HCT). Nonetheless, cGVHD remains a leading cause of post-transplant morbidity and mortality in children and adolescents, which is particularly relevant given the longer life-expectancy after HCT (measured in decades) compared to older adults. To address this knowledge gap, leaders of the Pediatric Transplant and Cellular Therapy Consortium convened a multidisciplinary taskforce of experts in pediatric cGVHD and HCT late effects known as RESILIENT after Chronic GVHD (Research and Education towards Solutions for Late effects to Innovate, Excel, and Nurture after cGVHD). Our goals were to define: (1) the current state of understanding about how cGVHD impacts long-term survivorship in children transplanted <18 yr of age; (2) practical aspects of care to help clinicians managing long-term pediatric cGVHD survivors; and (3) develop a research framework for the next decade to further our knowledge. Four working groups were formed, each tasked with addressing a unique theme: (1) cGVHD natural history (phases of cGVHD) and its impact on clinicians' ability to taper and durably discontinue systemic therapy; (2) organ dysfunction and immune reconstitution in relation to survivorship; (3) how cGVHD and its treatment impact growth, metabolism, and development in children; and (4) psychosocial health and patient reported outcomes. The 4 groups met before the 2024 BMT Tandem Meeting in San Antonio, Texas, and then convened a larger in-person RESILIENT conference held on February 20, 2024, at the Tandem meeting to put forth recommendations from their respective working groups and garner feedback. These recommendations are now presented in a series of 4 manuscripts. This current manuscript focuses on the first theme and discusses the phases of cGVHD, challenges in differentiating clinically active from quiescent cGVHD in clinical practice, and the resultant difficulties in determining when and if to taper systemic therapy. To overcome these challenges, we propose revised categorization of long-term cGVHD outcomes and practical recommendations for clinicians and researchers around the long-term follow-up for these patients, including determining when and if to taper systemic therapy, along with the integration of non-immunosuppressive supportive care interventions.

Indexed as

Cell- and Tissue-Based TherapyGraft vs Host DiseaseHematopoietic Stem Cell TransplantationAdolescentChildChild, PreschoolChronic DiseaseHumansSurvivorshipChronic GVHDNatural historyPhasesTherapy discontinuation

Identifiers

PMID39701289
PMCPMC11816905

What OpenQuestion holds

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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.