Evidence map›Paper›PMID 37226713›Full record

Observational studyHaematologica2024

Patient-reported treatment response in chronic graft-

Annie Im, Iskra Pusic, Lynn Onstad, Carrie L Kitko, Betty K Hamilton, Amin M Alousi, Mary E Flowers, Stefanie Sarantopoulos, Paul Carpenter, Jennifer White and 6 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Haematologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 8 citations in OpenAlex.

  1. Fatigue and quality of life in the early phase after allogeneic hematopoietic stem cell transplantation: dynamics and the impact of graft-versus-host disease.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 13 institutions in 2 countries.

Annie ImUniversity of Pittsburgh/UPMC Hillman Cancer Center, Pittsburgh, PA.
Iskra PusicDivision of Medicine and Oncology, Washington University, Saint Louis, Missouri.
Lynn OnstadClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Carrie L KitkoPediatric Blood and Marrow Transplantation Program, Vanderbilt University Medical Center, Nashville, Tennessee.
Betty K HamiltonBlood and Marrow Transplantation, Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH.
Amin M AlousiDepartment of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX.
Mary E FlowersClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Stefanie SarantopoulosDivision of Hematological Malignancies and Cellular Therapy, Duke University Department of Medicine, Duke Cancer Institute, Durham, North Carolina.
Paul CarpenterClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Jennifer WhiteLeukemia/Bone Marrow Transplant Program of British Columbia, British Columbia Cancer Agency, Vancouver, BC.
Sally AraiDepartment of Medicine, Division of Blood and Marrow Transplantation, Stanford University School of Medicine, Stanford, CA.
Najla El JurdiDivision of Hematology, Oncology and Transplantation, University of Minnesota Medical Center, Minneapolis, MN.
George ChenDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Corey CutlerDivision of Stem Cell Transplantation and Cellular Therapy, Dana-Farber Cancer Institute, Boston, MA.
Stephanie LeeClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Joseph PidalaBlood and Marrow Transplantation and Cellular Immunotherapy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL. joseph.pidala@moffitt.org.
Fred Hutch Cancer Center · USBC Cancer Agency · CACleveland Clinic · USDana-Farber Cancer Institute · USDuke University · USMoffitt Cancer Center · USRoswell Park Comprehensive Cancer Center · USStanford University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Minnesota Medical Center · USUPMC Hillman Cancer Center · USVanderbilt University Medical Center · USWashington University in St. Louis · US

Funding

Improving Outcomes Assessment in Chronic GVHDR01CA118953 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEE, STEPHANIE J · 2011 to 2025
$8.3M
NCI NIH HHS R01 CA118953
6 · The paper itself

Abstract

Chronic graft-versus-host disease (GvHD) treatment response is assessed using National Institutes of Health (NIH) Consensus Criteria in clinical trials, and by clinician assessment in routine practice. Patient-reported treatment response is central to the experience of chronic GvHD manifestations as well as treatment benefit and toxicity, but how they correlate with clinician- or NIH-responses has not been well-studied. We aimed to characterize 6-month patientreported response, determine associated chronic GvHD baseline organ features and changes, and evaluate which patientreported quality of life and chronic GvHD symptom burden measures correlated with patient-reported response. From two nationally representative Chronic GVHD Consortium prospective observational studies, 382 subjects were included in this analysis. Patient and clinician responses were categorized as improved (completely gone, very much better, moderately better, a little better) versus not improved (about the same, a little worse, moderately worse, very much worse). At six months, 270 (71%) patients perceived chronic GvHD improvement, while 112 (29%) perceived no improvement. Patient-reported response had limited correlation with either clinician-reported (kappa 0.37) or NIH chronic GvHD response criteria (kappa 0.18). Notably, patient-reported response at six months was significantly associated with subsequent failure-free survival. In multivariate analysis, NIH responses in eye, mouth, and lung had significant association with 6-month patient-reported response, as well as a change in Short Form 36 general health and role physical domains and Lee Symptom Score skin and eye changes. Based on these findings, patient-reported responses should be considered as an important complementary endpoint in chronic GvHD clinical trials and drug development.

Indexed as

Bronchiolitis Obliterans SyndromeGraft vs Host DiseaseHematopoietic Stem Cell TransplantationChronic DiseaseHumansPatient Reported Outcome MeasuresQuality of Life

Identifiers

PMID37226713
PMCPMC10772515
OpenAlexW4378172267

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.