Evidence map›Paper›PMID 26256940›Full record

Trial reportBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2016

Atorvastatin for the Prophylaxis of Acute Graft-versus-Host Disease in Patients Undergoing HLA-Matched Related Donor Allogeneic Hematopoietic Stem Cell Transplantation (allo-HCT).

Yvonne A Efebera, Susan Geyer, Leslie Andritsos, Sumithira Vasu, Samantha Jaglowski, Anissa Bingman, William Blum, Rebecca Klisovic, Craig C Hofmeister, Don M Benson and 19 more

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  5. Observational
  6. Review
  7. Article
  8. Review
  9. Current approaches to prevent and treat GVHD after allogeneic stem cell transplantation.Hematology. American Society of Hematology. Education Program · 2018
    Review
  10. Review
  11. 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

29 authors at 2 institutions in 1 country.

Yvonne A EfeberaDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio. Electronic address: yvonne.efebera@osumc.edu.
Susan GeyerDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio; Health Informatics Institute College of Medicine, University of South Florida, Tampa, Florida.
Leslie AndritsosDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Sumithira VasuDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Samantha JaglowskiDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Anissa BingmanDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
William BlumDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Rebecca KlisovicDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Craig C HofmeisterDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Don M BensonDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Sam PenzaDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Patrick ElderDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Katie CortrightDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Rhonda KitzlerDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Kevin CoombesCenter for Biostatistics, Department of Biomedical Informatics, The Ohio State University, Columbus, Ohio.
Lynn O'DonnellDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Beth DaneaultDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Hillary BradburyDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Jianying ZhangCenter for Biostatistics, Department of Biomedical Informatics, The Ohio State University, Columbus, Ohio.
Xilin ChenDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Sabrina GarmanDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Parvathi RanganathanDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Xueyan YuDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Jessica HofstetterDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Jianhua YuDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Ramiro GarzonDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Scott R ScrapeDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Gerard LozanskiDepartment of Pathology, The Ohio State University, Columbus, Ohio.
Steven M DevineDivision of Hematology, Department of Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
The Ohio State University · USUniversity of South Florida · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
NCI NIH HHS K12 CA133250NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

Statins possess potent immunomodulatory effects that may play a role in preventing acute graft-versus-host disease (aGVHD) after allogeneic hematopoietic cell transplantation (allo-HCT). We performed a phase II study of atorvastatin for aGVHD prophylaxis when given to allo-HCT recipients and their HLA-matched sibling donors. Atorvastatin (40 mg/day) was administered to sibling donors, beginning 14 days before the anticipated start of stem cell collection. Allo-HCT recipients (n = 40) received atorvastatin (40 mg/day) in addition to standard aGVHD prophylaxis. The primary endpoint was cumulative incidence of grades II to IV aGVHD at day 100. Atorvastatin was well tolerated, with no attributable grades III to IV toxicities in donors or their recipients. Day 100 and 180 cumulative incidences of grades II to IV aGVHD were 30% (95% confidence interval [CI], 17% to 45%) and 40% (95% CI, 25% to 55%), respectively. One-year cumulative incidence of chronic GVHD was 43% (95% CI, 32% to 69%). One-year nonrelapse mortality and relapse incidences were 5.5% (95% CI, .9% to 16.5%) and 38% (95% CI, 18% to 47%), respectively. One-year progression-free and overall survival rates were 54% (95% CI, 38% to 71%) and 82% (95% CI, 69% to 94%). One-year GVHD-free, relapse-free survival was 27% (95% CI, 16% to 47%). These results did not differ from our historical control subjects (n = 96). Although safe and tolerable, the addition of atorvastatin did not appear to provide any benefit to standard GVHD prophylaxis alone.

Indexed as

Hematopoietic Stem Cell TransplantationHistocompatibility TestingTissue DonorsAcute DiseaseAdultAgedAllograftsAtorvastatinDisease-Free SurvivalFemaleGraft vs Host DiseaseHumansMaleMiddle AgedSurvival RateAtorvastatinAllogeneic hematopoietic stem cell transplantAtorvastatinGraft-versus-host-disease

Identifiers

PMID26256940
PMCPMC4706501
OpenAlexW2197610420

What OpenQuestion holds

Textmetadata
LicenceTDM
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.