4.7 Article

Atorvastatin induces adrenal androgen downshift in men with prostate cancer: A post Hoc analysis of a pilot adaptive Randomised clinical trial

Journal

EBIOMEDICINE
Volume 68, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ebiom.2021.103432

Keywords

Prostate cancer; Serum adrenal androgens; Prostatic tissue adrenal androgens; Statins; Clinical trial

Funding

  1. Finnish Cultural Foundation
  2. Finnish Cancer Society
  3. Academy of Finland
  4. Expert Responsibility Area of the Tampere University Hospital
  5. Biocenter Finland
  6. Biocenter Kuopio

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The study investigated the impact of atorvastatin on steroid profiles in the serum and prostatic tissue of men with prostate cancer. The findings suggest that atorvastatin may influence adrenal androgen levels in the serum and possibly in the prostate, indicating a potential for improving androgen deprivation therapy efficacy.
Background: Prostate cancer (PCa) progression depends on androgen receptor activity. Cholesterol is required for biosynthesis of all steroid hormones, including androgens. Impact of cholesterol-lowering statins on androgens is unknown. We explored atorvastatin influence on serum and prostatic tissue steroidomic profiles (SP) to expose novel pathways for limiting androgen concentration in men with PCa. Methods: This is a pre-planned post hoc analysis of ESTO-1 pilot randomised, double-blinded, clinical trial. Statin naive men, scheduled for radical prostatectomy due to localised PCa, were randomised 1:1 to use daily 80 mg of atorvastatin or placebo before the surgery for a median of 28 days. Participants were recruited and treated at the Pirkanmaa Hospital District, Tampere, Finland. 108 of the 158 recruited men were included in the analysis based on sample availability for hormone profiling. Serum and prostatic tissue steroid profiles were determined using liquid chromatography mass spectrometry. Wilcoxon rank sum test and bootstrap confidence intervals (CI) were used to analyse the difference between placebo and atorvastatin arms. Findings: Most serum and prostatic steroids, including testosterone and dihydrotestosterone, were not associated with atorvastatin use. However, atorvastatin use induced serum SP changes in 11-ketoandrostenedione (placebo 960pM, atorvastatin 617.5pM, p-value <0.0001, median difference-342.5; 95% CI-505.23 -188.98).In the prostatic tissue, atorvastatin was associated with plausible downshift in 11-ketodihydrotestosterone (placebo 25.0pM in 100 mg tissue/1 mL saline, atorvastatin 18.5pM in 100 mg tissue/1 mL saline, p-value 0.027, median difference-6.53; 95% CI-12.8 -0.29); however, this association diminished after adjusting for multiple testing. No serious harms were reported. Interpretation: Atorvastatin was associated with adrenal androgen downshift in the serum and possibly in the prostate. The finding warrants further investigation whether atorvastatin could improve androgen deprivation therapy efficacy. Funding: Funded by grants from the Finnish Cultural Foundation, Finnish Cancer Society, Academy of Finland, and the Expert Responsibility Area of the Tampere University Hospital. Clinicaltrials.gov identifier: NCT01821404. (C) 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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