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A clinical trial of lovastatin for modification of biomarkers associated with breast cancer risk

Overview of attention for article published in Breast Cancer Research and Treatment, October 2013
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Title
A clinical trial of lovastatin for modification of biomarkers associated with breast cancer risk
Published in
Breast Cancer Research and Treatment, October 2013
DOI 10.1007/s10549-013-2739-z
Pubmed ID
Authors

Shaveta Vinayak, Erich J. Schwartz, Kristin Jensen, Jafi Lipson, Elizabeth Alli, Lisa McPherson, Adrian M. Fernandez, Vandana B. Sharma, Ashley Staton, Meredith A. Mills, Elizabeth A. Schackmann, Melinda L. Telli, Ani Kardashian, James M. Ford, Allison W. Kurian

Abstract

Pre-clinical and epidemiologic studies provide rationale for evaluating lipophilic statins for breast cancer prevention. We conducted a single-arm, biomarker modulation trial of lovastatin among women with increased risk of breast cancer. Eligibility criteria included a deleterious germline mutation in BRCA1, BRCA2, CDH1, or TP53; lifetime breast cancer risk of ≥20 % as estimated by the Claus model; or personal history of estrogen receptor and progesterone receptor-negative breast cancer. Participants received 40 mg of lovastatin orally twice daily for 6 months. We evaluated the following biomarkers before and after lovastatin use: breast duct cytology (primary endpoint), serum lipids, C-reactive protein, insulin-like growth factor-1, IGF binding protein-3, lipid peroxidation, oxidative DNA damage, 3-hydroxy-3-methylglutaryl CoA reductase genotype, and mammographic density. Thirty women were enrolled, and 26 (86.7 %) completed the study. For the primary endpoint of changes in breast duct cytology sampled by random periareolar fine needle aspiration, most participants [57.7 %, 95 % confidence interval (CI) 38.9-74.5 %] showed no change after lovastatin; 19.2 % (CI 8.1-38.3 %) had a favorable change in cytology, 7.7 % (95 % CI 1.0-25.3 %) had an unfavorable change, and 15.4 % (95 % CI 5.5-34.2 %) had equivocal results due to acellular specimens, usually after lovastatin. No significant changes were observed in secondary biomarker endpoints. The study was generally well-tolerated: 4 (13.3 %) participants did not complete the study, and one (3.8 %) required a dose reduction. This trial was technically feasible, but demonstrated no significant biomarker modulation; contributing factors may include insufficient sample size, drug dose and/or duration. The results are inconclusive and do not exclude a favorable effect on breast cancer risk.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 64 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 1 2%
Unknown 63 98%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 10 16%
Student > Ph. D. Student 9 14%
Researcher 8 13%
Student > Master 8 13%
Lecturer 5 8%
Other 13 20%
Unknown 11 17%
Readers by discipline Count As %
Medicine and Dentistry 29 45%
Biochemistry, Genetics and Molecular Biology 5 8%
Agricultural and Biological Sciences 5 8%
Nursing and Health Professions 2 3%
Pharmacology, Toxicology and Pharmaceutical Science 2 3%
Other 9 14%
Unknown 12 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 November 2013.
All research outputs
#20,211,690
of 22,733,113 outputs
Outputs from Breast Cancer Research and Treatment
#4,103
of 4,649 outputs
Outputs of similar age
#185,226
of 212,669 outputs
Outputs of similar age from Breast Cancer Research and Treatment
#69
of 77 outputs
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