4.7 Article

Changes in bone and mineral homeostasis after short-term androgen deprivation therapy with or without androgen receptor signalling inhibitor - substudy of a single-centre, double blind, randomised, placebo-controlled phase 2 trial

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EBIOMEDICINE
卷 97, 期 -, 页码 -

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DOI: 10.1016/j.ebiom.2023.104817

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Androgen deprivation therapy; Androgen receptor signalling inhibitor; Bone turnover marker; Prostate cancer; Stable calcium isotope

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Prostate cancer patients treated with androgen deprivation therapy (ADT) have an increased risk of bone loss. This study suggests that 12 weeks of ADT in non-metastatic PCa patients results in early bone loss, and additional treatment with ARSI does not seem to worsen bone loss in the early phase. Future studies should investigate if these early biomarkers can predict fracture risk and be used in clinical practice for monitoring bone health in PCa patients undergoing ADT.
Background Prostate cancer (PCa) patients treated with androgen deprivation therapy (ADT) have an increased fracture risk. Exploring biomarkers for early bone loss detection is of great interest. Methods Pre-planned substudy of the ARNEO-trial (NCT03080116): a double blind, randomised, placebo -controlled phase 2 trial performed in high-risk PCa patients without bone metastases between March 2019 and April 2021. Patients were 1:1 randomised to treatment with gonadotropin-releasing hormone antagonist (degarelix) + androgen receptor signalling inhibitor (ARSI; apalutamide) versus degarelix + matching placebo for 12 weeks prior to prostatectomy. Before and following ADT, serum and 24-h urinary samples were collected. Primary endpoints were changes in calcium-phosphate homeostasis and bone biomarkers. Findings Of the 89 randomised patients, 43 in the degarelix + apalutamide and 44 patients in the degarelix + placebo group were included in this substudy. Serum corrected calcium levels increased similarly in both treatment arms (mean difference +0.04 mmol/L, 95% confidence interval, 0.02; 0.06), and parathyroid hormone and 1,25-dihydroxyvitamin D3 levels decreased. Bone resorption markers increased, and stable calcium isotope ratios reflecting net bone mineral balance decreased in serum and urine similarly in both groups. Interpretation This exploratory substudy suggests that 12 weeks of ADT in non-metastatic PCa patients results in early bone loss. Additional treatment with ARSI does not seem to more negatively influence bone loss in the early phase. Future studies should address if these early biomarkers are able to predict fracture risk, and can be implemented in clinical practice for follow-up of bone health in PCa patients under ADT. Funding Research Foundation Flanders; KU Leuven; University-Hospitals-Leuven.Copyright (c) 2023 The Author(s). 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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