Evidence map›Paper›PMID 25529383›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2015

National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2014 Diagnosis and Staging Working Group report.

Madan H Jagasia, Hildegard T Greinix, Mukta Arora, Kirsten M Williams, Daniel Wolff, Edward W Cowen, Jeanne Palmer, Daniel Weisdorf, Nathaniel S Treister, Guang-Shing Cheng and 20 more

13 registry-linked trialsAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 13 registered trials, which are not on this map. Cited by 1,461 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,461citing 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.

NCT00896493 phase2completednot on this map

A Phase II Study of Non-myeloablative Allogeneic Transplantation Using Total Lymphoid Irradiation (TLI) and Antithymocyte Globulin (ATG) In Patients With Cutaneous T Cell Lymphoma

TypeinterventionalSponsorStanford UniversityRan2009 to 2022Enrolled38ConditionsMycoses, Sezary Syndrome, Lymphoma, T-Cell, Cutaneous, Bone Marrow Transplant FailureArmsanti-thymocyte globulin, cyclosporine, Lymphoid radiation
NCT02123966 phase2terminatednot on this map

An Open Label Phase II Trial of Topical Sirolimus for the Treatment of Refractory Oral Chronic Graft-versus-Host-Disease

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2014 to 2016Enrolled10ConditionsChronic Graft-versus-Host-Disease, Oral Mucosal Disease Due to Graft-versus-host DiseaseArmsSirolimus
NCT02206035 phase2completednot on this map

Phase II Open-Label Trial of Tacrolimus/Methotrexate and Tocilizumab for the Prevention of Acute Graft-Versus-Host Disease After Allogeneic Hematopoietic Stem Cell Transplantation

TypeinterventionalSponsorWilliam R. Drobyski, MDRan2014 to 2018Enrolled45ConditionsHematopoietic Stem Cell TransplantationArmsTacrolimus, Methotrexate, Tocilizumab
NCT02626715 phase2completednot on this map

A Phase II Study of Myeloablative and Reduced-Intensity Conditioning Regimens for Children and Young Adults With Acute Myeloid Leukemia or Myelodysplastic Syndrome Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

TypeinterventionalSponsorRandy WindreichRan2015 to 2023Enrolled21ConditionsAcute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), Hematopoietic Stem Cell Transplant (HSCT)ArmsReduced-Intensity Conditioning Regimen, Myeloablative Conditioning Regimen
NCT03267186 phase2completednot on this mapstarted 2017, after this paper: background citation

A Phase 2 Study of Ibrutinib Maintenance After Reduced-Intensity Conditioning and Allogeneic Hematopoietic Cell Transplantation for Acute Leukemia

TypeinterventionalSponsorAndrew RezvaniRan2017 to 2021Enrolled8ConditionsAcute Biphenotypic Leukemia, Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Chronic Myelogenous Leukemia, BCR-ABL1 PositiveArmsIbrutinib, Laboratory Biomarker Analysis
NCT03602599 completednot on this mapstarted 2018, after this paper: background citation

Natural History of Chronic Graft-versus-Host Disease in the Oral Cavity of Patients Following Allogeneic Hematopoietic Stem Cell Transplant and Including Healthy Controls

TypeobservationalSponsorNational Institute of Dental and Craniofacial Research (NIDCR)Ran2018 to 2026Enrolled190ConditionsGraft Versus Host Disease
NCT04946721 recruitingnot on this mapstarted 2022, after this paper: background citation

2177GCCC: Identifying Novel Treatment Targets and Biomarkers for Ocular Surface Disease in Patients With Ocular Graft vs Host Disease (oGVHD) a Biobank Study

TypeobservationalSponsorUniversity of Maryland, BaltimoreRan2022 to 2027Enrolled150ConditionsDry Eye Disease, oGVHDArmsThe standard care exam and biological specimens' collection
NCT06348602 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

Evaluation of Safety and Efficacy for the Prevention of Ocular Graft-versus-host Disease With Ophthalmic Tacrolimus vs. Ophthalmic Cyclosporine in Non-myeloablative Allogeneic Hematopoietic Stem Cell Transplant Recipients

TypeinterventionalSponsorHospital Universitario Dr. Jose E. GonzalezRan2023 to 2025Enrolled60ConditionsOcular Graft-versus-host DiseaseArmsCyclosporine ophthalmic solution 0.1%, Tacrolimus ophthalmic ointment 0.03%
NCT06756061 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Nation-wide, Multi-center, Prospective, Randomized, Parallel-group, Open-label, Investigator Initiated Pilot Study to Evaluate Efficacy and Safety of Systemic Corticosteroid Plus Ruxolitinib as First-line Therapy in Patients With New-onset Moderate to Severe Chronic Graft-versus-host Disease

TypeinterventionalSponsorByung-Sik ChoRan2025 to 2029Enrolled88ConditionsGVHD - Graft-Versus-Host Disease, Neoplasms, Haematopoietic Stem Cell TransplantationArmsPrednisone + Jakavi(ruxolitinib), Prednisone
NCT06845592 narecruitingnot on this mapstarted 2025, after this paper: background citation

SHARP - Safely Delivered Targeted High-dose Irradiation Followed by Adoptive Immunotherapy with Regulatory and Conventional T Cells to Increase Potency of Hematopoietic Stem Cell Transplantation in High-risk Acute Leukemia

TypeinterventionalSponsorUniversity Of PerugiaRan2025 to 2031Enrolled51ConditionsAcute Myeloid Leukaemia (AML), Acute Lymphoblastic Leukemia ALL, High Risk Leukaemia, Leukaemia RelapseArmstotal marrow/lymphoid irradiation
NCT07078721 phase2not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Efficacy and Safety Study of Umbilical Cord Blood Transplantation (UCBT) With Total Marrow Irradiation (TMI)-Based Conditioning Regimen for Adults With Refractory/Relapsed Aplastic Anemia (AA).

TypeinterventionalSponsorInstitute of Hematology & Blood Diseases Hospital, ChinaRan2025 to 2028Enrolled11ConditionsAplastic Anemia IdiopathicArmsTotal Marrow Irradiation, Fludarabine (FLU), Melphalan (Mel)
NCT07502118 phase2 / phase3recruitingnot on this mapstarted 2025, after this paper: background citation

An Open-Label, Multicenter Phase 2-3 Clinical Study of Anti-CD19 Chimeric Antigen Receptor T Cells (Talikabtagene Autoleucel) in Patients With Relapsed/Refractory B-Cell Malignancies (NexCAR19)

TypeinterventionalSponsorHealth Institutes of TurkeyRan2025 to 2030Enrolled40ConditionsRelapsed/Refractory B-cell Acute Lymphoblastic Leukemia (B-ALL), Relapsed/Refractory Non-Hodgkin Lymphoma, Diffuse Large B-Cell Lymphoma (DLBCL), High-grade B-cell Lymphoma (HGBCL)ArmsTalikabtagene Autoleucel
NCT07576699 phase1 / phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

CK0802 for Treatment of Steroid Refractory Graft vs. Host Disease (GVHD)

TypeinterventionalSponsorCellenkos, Inc.Ran2026 to 2029Enrolled12ConditionsSteroid Refractory Graft Versus Host DiseaseArmsCK0802 (Allogeneic, Cryopreserved, Cord blood-derived T-regulatory cells, cells that are not HLA matched)
3 · Its place in the literature

Who cites it

1,461 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  17. Gynaecological complications and vulvovaginal graft-versus-host disease after allogeneic haematopoietic stem cell transplantation: a retrospective study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Observational
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1,401 more citing papers are in PubMed but not listed here.

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

30 authors.

Madan H JagasiaDepartment of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
Hildegard T GreinixDepartment of Internal Medicine, Medical University of Vienna, Vienna, Austria.
Mukta AroraDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Kirsten M WilliamsCenter for Cancer Research National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Department of Blood and Marrow Transplantation, Children's National Health System, Washington, District of Columbia.
Daniel WolffDepartment of Internal Medicine, University of Regensburg, Regensburg, Germany.
Edward W CowenCenter for Cancer Research National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Jeanne PalmerDepartment of Hematology Oncology/Blood and Marrow Transplant, Mayo Clinic Arizona, Phoenix, Arizona.
Daniel WeisdorfDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Nathaniel S TreisterDepartment of Surgery, Division of Oral Medicine and Dentistry, Brigham and Women's Hospital, Boston, Massachusetts.
Guang-Shing ChengClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Holly KerrHematology Department, BC Cancer Agency, Vancouver, British Columbia, Canada.
Pamela StrattonPediatric and Reproductive Endocrinology Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
Rafael F DuarteDepartment of Hematology, Institut Catala d'Oncologia, Barcelona, Spain.
George B McDonaldClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Yoshihiro InamotoDivision of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Afonso VigoritoHematology and Hemotherapy Center, Hemocentro Unicamp, Campinas, Sao Paulo, Brazil.
Sally AraiDepartment of Blood and Marrow Transplantation, Stanford University Medical Center, Stanford, California.
Manuel B DatilesThe Eye Clinic, National Eye Institute, National Institutes of Health, Bethesda, Maryland.
David JacobsohnDepartment of Blood and Marrow Transplantation, Children's National Health System, Washington, District of Columbia.
Theo HellerLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Disease, National Institutes of Health, Bethesda, Maryland.
Carrie L KitkoBlood and Marrow Transplant Program, University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan.
Sandra A MitchellDepartment of Applied Research Cancer Control and Population Sciences, National Institutes of Health, Bethesda, Maryland.
Paul J MartinClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Howard ShulmanClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Roy S WuCancer Therapy Evaluation Program, National Institutes of Health, Bethesda, Maryland.
Corey S CutlerDivision of Hematologic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Georgia B VogelsangOncology Department, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Stephanie J LeeClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Steven Z PavleticCenter for Cancer Research National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Mary E D FlowersClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington. Electronic address: mflowers@fredhutch.org.

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
Improving Outcomes Assessment in Chronic GVHDR01CA118953 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2011 to 2025
$8.3M
Chronic graft-versus-host diseaseZIABC011549 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI COWEN, EDWARD · 2014 to 2021
$5.2M
Improving Outcomes Assessment in Chronic GVHDU01CA118953 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2007 to 2010
$3.1M
Safety and Immunogenicity of Gardasil post stem cell transplantationZIAHD008900 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI STRATTON, PAMELA · 2010 to 2016
$1.2M
A Randomized, Controlled, Double-Masked, Clinical Trial of Autologous Serum Eye Drops for Severe Ocular Chronic Graft-versus-Host Disease (GVHD) in Hematopoietic Stem Cell Transplant (HSCT) PatientsZIAEY000540 · NEI · NATIONAL EYE INSTITUTE · PI DATILES, MANUEL B · 2014 to 2016
$795k
NCI NIH HHS CA118953NCI NIH HHS CA18029NCI NIH HHS P01 CA018029NCI NIH HHS R01 CA118953NCI NIH HHS U01 CA118953
6 · The paper itself

Abstract

The 2005 National Institutes of Health (NIH) Consensus Conference proposed new criteria for diagnosing and scoring the severity of chronic graft-versus-host disease (GVHD). The 2014 NIH consensus maintains the framework of the prior consensus with further refinement based on new evidence. Revisions have been made to address areas of controversy or confusion, such as the overlap chronic GVHD subcategory and the distinction between active disease and past tissue damage. Diagnostic criteria for involvement of mouth, eyes, genitalia, and lungs have been revised. Categories of chronic GVHD should be defined in ways that indicate prognosis, guide treatment, and define eligibility for clinical trials. Revisions have been made to focus attention on the causes of organ-specific abnormalities. Attribution of organ-specific abnormalities to chronic GVHD has been addressed. This paradigm shift provides greater specificity and more accurately measures the global burden of disease attributed to GVHD, and it will facilitate biomarker association studies.

Indexed as

BiomarkersChronic DiseaseClinical Trials as TopicConsensusConsensus Development Conferences, NIH as TopicFemaleGraft vs Host DiseaseHumansMaleOrgan SpecificityPractice Guidelines as TopicUnited StatesBiomarkersChronic graft-versus-host diseaseDiagnosisNational Institutes of HealthStaging

Identifiers

PMID25529383
PMCPMC4329079

What OpenQuestion holds

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Read underepoch 390

Registered trials

and 7 more above

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.