Evidence map›Paper›PMID 29128193›Full record

Trial reportClinical breast cancer2018

Vitamin D Levels, Vitamin D Receptor Polymorphisms, and Inflammatory Cytokines in Aromatase Inhibitor-Induced Arthralgias: An Analysis of CCTG MA.27.

Polly Niravath, Bingshu Chen, Judy-Anne W Chapman, Sandeep K Agarwal, Robert L Welschhans, Tim Bongartz, Krishna R Kalari, Lois E Shepherd, John Bartlett, Kathleen Pritchard and 6 more

Open access · greenAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Clinical breast cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
0.9field-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

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Genome-wide association study of aromatase inhibitor discontinuation due to musculoskeletal symptoms.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
    Trial
  5. Trial
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  7. Musculoskeletal symptoms associated with aromatase inhibitors in the treatment of early breast cancer: A scoping review of risk factors and outcomes.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  8. Review
  9. A Cohort Study to Evaluate Genetic Predictors of Aromatase Inhibitor Musculoskeletal Symptoms: Results from ECOG-ACRIN E1Z11.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
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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

16 authors at 8 institutions in 2 countries.

Polly NiravathDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX. Electronic address: paniravath@houstonmethodist.org.
Bingshu ChenDepartment of Internal Medicine, Queens University Cancer Research Institute, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
Judy-Anne W ChapmanDepartment of Internal Medicine, Queens University Cancer Research Institute, Queen's Cancer Research Institute, Kingston, Ontario, Canada.
Sandeep K AgarwalDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX.
Robert L WelschhansDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX.
Tim BongartzDepartment of Internal Medicine, Vanderbilt University, Nashville, TN.
Krishna R KalariDepartment of Internal Medicine, Mayo Clinic, Rochester, MN.
Lois E ShepherdDepartment of Internal Medicine, Queens University Cancer Research Institute, Kingston, Ontario, Canada.
John BartlettDepartment of Internal Medicine, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Kathleen PritchardDepartment of Internal Medicine, Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada.
Karen GelmonDepartment of Internal Medicine, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
Susan G HilsenbeckDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX.
Mothaffar F RimawiDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX.
C Kent OsborneDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX.
Paul E GossDepartment of Internal Medicine, Harvard Medical School, Boston, MA.
James N IngleDepartment of Internal Medicine, Mayo Clinic, Rochester, MN.
Baylor College of Medicine · USQueen's University · CAMayo Clinic in Arizona · USBC Cancer Agency · CAHarvard University · USOntario Institute for Cancer Research · CASunnybrook Health Science Centre · CAVanderbilt University · US

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI Fergus Joseph Couch · 2005 to 2026
$49.9M
Translational Research in Breast Cancer (SPORE)P50CA186784 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MATTHEW J ELLIS · 2014 to 2026
$24.5M
NCI NIH HHS P50 CA116201NCI NIH HHS P50 CA186784
6 · The paper itself

Abstract

backgroundApproximately half of women taking aromatase inhibitor (AI) therapy develop AI-induced arthralgia (AIA), and many might discontinue AI therapy because of the pain. Using plasma samples from the MA.27 study, we assessed several factors potentially associated with AIA. PATIENTS AND

methodsMA.27 is a phase III adjuvant trial comparing 2 AIs, exemestane versus anastrozole. Within an 893-participant nested case-control AIA genome-wide association study, we nested a 72 AIA case-144 control assessment of vitamin D plasma concentrations, corrected for seasonal and geographic variation. We also examined 9 baseline inflammatory cytokines: interleukin (IL)-1β, IL-6, tumor necrosis factor-α, interferon (IFN)γ, IL-10, IL-12p70, IL-17, IL-23, and chemokine ligand (CCL)-20. Finally, we analyzed the multivariate effects of baseline factors: vitamin D level, previously identified musculoskeletal single nucleotide polymorphisms, age, body mass index, and vitamin D receptor (VDR) Fok-I variant genotype on AIA development.

resultsChanges in vitamin D from baseline to 6 months were not significantly different between cases and controls. Elevated inflammatory cytokine levels were not associated with development of AIA. The multivariate model included no clinical factors associated with AIA. However, women with the VDR Fok-I variant genotype were more likely to have a lower IL-1β level (P = .0091) and less likely to develop AIA after 6 months of AI compared with those with the wild type VDR (P < .0001).

conclusionIn this nested case-control correlative study, vitamin D levels were not significantly associated with development of AIA; however, patients with the Fok-I VDR variant genotype were more likely to have a significant reduction in IL-1β level, and less likely to develop AIA.

Indexed as

AgedAged, 80 and overAnastrozoleAndrostadienesAromatase InhibitorsArthralgiaBreast NeoplasmsCase-Control StudiesChemotherapy, AdjuvantFemaleGenetic Predisposition to DiseaseHumansInterleukin-1betaMastectomyMiddle AgedPolymorphism, Single NucleotideAnastrozoleAndrostadienesAromatase InhibitorsexemestaneIL1B protein, humanInterleukin-1betaReceptors, CalcitriolVDR protein, humanVitamin DAromatase inhibitor-induced arthralgiasIL-1 betaInflammatory cytokinesVitamin DVitamin D receptor polymorphisms

Identifiers

PMID29128193
PMCPMC7469602
OpenAlexW2766893338

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.