Evidence map›Paper›PMID 27532508›Full record

Trial reportJAMA oncology2016

Comparison of Patient-Reported Outcomes in 5-Year Survivors Who Received Bone Marrow vs Peripheral Blood Unrelated Donor Transplantation: Long-term Follow-up of a Randomized Clinical Trial.

Stephanie J Lee, Brent Logan, Peter Westervelt, Corey Cutler, Ann Woolfrey, Shakila P Khan, Edmund K Waller, Richard T Maziarz, Juan Wu, Bronwen E Shaw and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00075816 (A Phase III Randomized, Multicenter Trial Comparing G-CSF Mobilized Peripheral Blood Stem Cell With Marrow Transplantation From Human Leukocyte Antigen), which is not on this map. Cited by 70 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 7 pooled it
10.7field-weighted citation impact, top 1% 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.

NCT00075816 phase3completednot on this map

A Phase III Randomized, Multicenter Trial Comparing G-CSF Mobilized Peripheral Blood Stem Cell With Marrow Transplantation From Human Leukocyte Antigen (HLA) Compatible Unrelated Donors (BMT CTN #0201)

TypeinterventionalSponsorMedical College of WisconsinRan2004 to 2014Enrolled551ConditionsLeukemia, Myeloproliferative Disorders, Myelodysplastic-Myeloproliferative DiseasesArmsAllogeneic bone marrow transplantation, Peripheral blood stem cell transplantation
3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 7 syntheses or guidelines pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Pooled it
  5. Pooled it
  6. Guideline
  7. Pooled it
  8. Improved Patient-Reported Outcomes With Post-Transplant Cyclophosphamide: A Quality-of-Life Evaluation and 2-Year Outcomes of BMT CTN 1703.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Trial
  9. Trial
  10. Trial
  11. Trial
  12. Peripheral Blood versus Bone Marrow from Unrelated Donors: Bone Marrow Allografts Have Improved Long-Term Overall and Graft-versus-Host Disease-Free, Relapse-Free Survival.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  13. CD56Haematologica · 2017
    Trial
  14. Article
  15. Chronic graft-versus-host disease.Nature reviews. Disease primers · 2026
    Review
  16. Article
  17. FACS-Based Assessment of Human Hematopoietic Stem and Progenitor Cells.International journal of molecular sciences · 2025
    Review
  18. Article
  19. Graft Source Choice.Advances in experimental medicine and biology · 2025
    Review
  20. Article

10 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

13 authors at 10 institutions in 1 country.

Stephanie J LeeClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Brent LoganDivision of Biostatistics, Medical College of Wisconsin, Milwaukee.
Peter WesterveltDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St Louis, Missouri.
Corey CutlerDivision of Hematologic Malignancies and Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Ann WoolfreyTransplantation Biology Department, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Shakila P KhanDivision of Pediatric Hematology-Oncology, Mayo Clinic, Rochester, Minnesota.
Edmund K WallerWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University, Atlanta, Georgia.
Richard T MaziarzAdult Blood and Marrow Stem Cell Transplant Program, Knight Cancer Institute, Oregon Health and Science University, Portland.
Juan WuEmmes Corporation, Rockville, Maryland.
Bronwen E ShawCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee.
Dennis ConferNational Marrow Donor Program, Minneapolis, Minnesota.
Mary M HorowitzCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee.
Claudio AnasettiDepartment of Blood and Marrow Transplantation, Moffitt Cancer Center, Tampa, Florida.
Medical College of Wisconsin · USFred Hutch Cancer Center · USDana-Farber Cancer Institute · USEmmes (United States) · USEmory University · USMayo Clinic · USMoffitt Cancer Center · USNational Marrow Donor Program · USOregon Health & Science University · USWashington University in St. Louis · US

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
Easy-to-read Informed Consent for HCT Clinical TrialsU10HL069294 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HOROWITZ, MARY MARESCA · 2011 to 2016
$43.8M
A Randomized Trial of Tac/MTX/bortezomib vs Tac/MTXplacebo in Allogeneic HSCTU10HL069249 · NHLBI · DANA-FARBER CANCER INST · PI ANTIN, JOSEPH H · 2011 to 2016
$1.1M
Sargrastim and Plerixafor vs. Filgrastim for Allogeneic Stem Cell MobilizationU10HL109137 · NHLBI · WASHINGTON UNIVERSITY · PI WESTERVELT, PETER · 2011 to 2016
$937k
NCI NIH HHS U24 CA076518NHLBI NIH HHS U10 HL069249NHLBI NIH HHS U10 HL069294NHLBI NIH HHS U10 HL109137
6 · The paper itself

Abstract

importanceBone marrow or peripheral blood from unrelated donors may be used for hematopoietic cell transplantation. Information about the relative success of transplantation with these 2 graft sources would help physicians and patients choose between them.

objectiveTo compare patient-reported outcomes between patients randomized to receive 1 of 2 graft types for unrelated donor transplantation. DESIGN, SETTING, AND

participantsThis follow-up of a randomized clinical trial included English- or Spanish-speaking patients 16 years or older participating in a multicenter randomized clinical trial of unrelated donor bone marrow (BM) vs peripheral blood (PB) (N = 551) in hematopoietic cell transplantation for hematologic neoplasms. Patient-reported outcomes were collected from patients at enrollment and 0.5, 1, 2, and 5 years after transplantation.

interventionsUnrelated donor BM or PB hematopoietic cell transplantation. MAIN OUTCOMES AND MEASURES: Functional Assessment of Cancer Therapy-Bone Marrow Transplant, Mental Health Inventory, occupational functioning, Lee Chronic Graft-vs-Host Disease Symptom Scale.

resultsAt 5 years after transplantation, 102 BM and 93 PB participants were alive and eligible for assessment (age ≥40 years or older: 104 [53.5%] male: 101 [51.8%]). The mean (SE) Mental Health Inventory Psychological Well-Being scores (78.9 [1.7] vs 72.2 [1.9]; P = .01; higher better) and Lee chronic graft-vs-host disease symptom scores (13.1 [1.5] vs 19.3 [1.6]; P = .004; lower better) were significantly better for BM recipients, adjusting for baseline scores and missing data. Recipients of BM were also more likely to be working full or part-time than recipients of PB (odds ratio, 1.5; 95% CI, 1.2-2.0; P = .002), adjusting for work status before transplantation. With a median follow-up of 73 months (range, 30-121 months) for survivors, no differences in survival (40% vs 39%; P = .84), relapse (32% vs 29%; P = .47), or treatment-related mortality (29% vs 32%; P = .44) between BM and PB were observed. CONCLUSIONS AND RELEVANCE: Recipients of unrelated donor BM had better psychological well-being, less burdensome chronic GVHD symptoms, and were more likely to return to work than recipients of PB at 5 years after transplantation. Bone marrow should be the standard of care for these types of transplant procedures.

trial registrationclinicaltrials.gov Identifier: NCT00075816.

Indexed as

AdolescentAdultAgedBone MarrowBone Marrow TransplantationFemaleFollow-Up StudiesHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedSurvival AnalysisUnrelated Donors

Identifiers

PMID27532508
PMCPMC5145732
OpenAlexW2516841633

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.