Evidence map›Paper›PMID 39677358›Full record

ArticleEClinicalMedicine2024

Vitamin D in patients with low tumor-burden indolent non-Hodgkin lymphoma treated with rituximab therapy (ILyAD): a randomized, phase 3 clinical trial.

Jonathan W Friedberg, Michael T Brady, Myla Strawderman, Brad S Kahl, Izidore S Lossos, Jonathon B Cohen, Patrick M Reagan, Carla Casulo, Barbara L Averill, Andrea Baran and 8 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

18 authors.

Jonathan W FriedbergWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
Michael T BradyWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
Myla StrawdermanDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, USA.
Brad S KahlSiteman Cancer Center, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.
Izidore S LossosSylvester Comprehensive Cancer Center, Division of Hematology, University of Miami Miller School of Medicine, Miami, FL, USA.
Jonathon B CohenWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Patrick M ReaganWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
Carla CasuloWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
Barbara L AverillDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX, USA.
Andrea BaranDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, USA.
Grerk SutamtewagulDivision of Hematology, Oncology and Blood & Marrow Transplantation, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
Paul M BarrWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
John P LeonardWeill Medical College of Cornell University and New York Presbyterian Hospital, New York, NY, USA.
John M AshtonWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
John G StrangDepartment of Imaging Sciences, University of Rochester, Rochester, NY, USA.
Francisco VegaDepartment of Hematopathology, MD Anderson Cancer Center, Houston, TX, USA.
Derick R PetersonWilmot Cancer Institute, University of Rochester, Rochester, NY, USA.
Loretta J NastoupilDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX, USA.

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
The Lymphoma Epidemiology of Outcomes (LEO) Cohort Study (Supplement)U01CA195568 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R, FLOWERS, CHRISTOPHER R · 2015 to 2025
$22.1M
Vitamin D and Follicular LymphomaR01CA214890 · NCI · UNIVERSITY OF ROCHESTER · PI FRIEDBERG, JONATHAN W · 2017 to 2022
$3.3M
NCATS NIH HHS UL1 TR002001NCI NIH HHS R01 CA214890NCI NIH HHS U01 CA195568
6 · The paper itself

Abstract

Background: There is a significant association between low vitamin D levels at diagnosis of indolent B-cell lymphomas and inferior overall survival (OS). To determine whether supplemental vitamin D improves event-free survival (EFS) in these patients, we conducted a comparative double-blind study of vitamin D Methods: In this phase 3, randomized, double-blind, placebo-controlled trial, patients with low tumor burden follicular, marginal zone or small lymphocytic lymphoma, age 18 or older, with stage two or greater disease and no prior systemic treatment were enrolled at 7 academic cancer centers. Patients were stratified by histology and FLIPI (Follicular Lymphoma International Prognostic Index) score and randomized 2:1 to receive 2000 IU vitamin D Findings: 206 evaluable patients (135 on vitamin D and 71 on placebo) were enrolled between September 2017 and March 2022 with a median EFS follow-up of 19.6 months (IQR, 9.3-33.5). The median age was 62 years (IQR, 54-70); 118 (57%) female; 182 (89%) white. At week 13 the mean vitamin D level increased to 41.6 ng/mL (SD 10.1) in the vitamin D arm vs. remaining stable (31.3 ng/mL, SD 11.2) in the placebo arm. There was insufficient evidence of a difference in EFS between the two arms (P = 0.26): three-year EFS in the vitamin D arm was 47.7% (95% CI, 39.0-58.4) compared to 49.5% (95% CI, 37.6-65.0) in the placebo arm. There was no difference in week 13 response between the arms (both 84%). Adverse events associated with vitamin D supplementation were rare. The median OS follow-up was 35.1 months (IQR, 22.9-45.1), overall survival was 96.6% (95% CI, 93.1-98.6) and there was no significant difference between the vitamin D and placebo arms (P = 0.47). Interpretation: As tested in this study, there is no benefit to routine vitamin D supplementation in patients with indolent lymphoma treated with rituximab. These results have implications for ongoing and planned studies of vitamin D supplementation in other malignancies. Funding: This study was funded by the National Institutes of Health, National Cancer Institute grant R01CA214890.

Indexed as

CholecalciferolLymphomaVitamin D

Identifiers

PMID39677358
PMCPMC11638608

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.