Abstract

PurposeStatins’ cholesterol-lowering efficacy is well-known. Recent epidemiological studies have found that inhibition of cholesterol synthesis may have beneficial effects on prostate cancer (PCa) patients, especially patients treated with androgen deprivation therapy (ADT). We evaluated statins’ effect on prostate cancer prognosis among patients treated with ADT.Materials and methodsOur study population consisted of 8253 PCa patients detected among the study population of the Finnish randomized study of screening for prostate cancer. These were limited to 4428 men who initiated ADT during the follow-up. Cox proportional regression model adjusted for tumor clinical characteristics and comorbidities was used to estimate hazard ratios for risk of PSA relapse after ADT initiation and prostate cancer death.ResultsDuring the median follow-up of 6.3 years after the ADT initiation, there were 834 PCa deaths and 1565 PSA relapses in a study cohort. Statin use after ADT was associated with a decreased risk of PSA relapse (HR 0.73, 95% CI 0.65–0.82) and prostate cancer death (HR 0.82; 95% CI 0.69–0.96). In contrast, statin use defined with a one-year lag (HR 0.89, 95% CI 0.76–1.04), statin use before ADT initiation (HR 1.12, 95% CI 0.96–1.31), and use in the first year on ADT (HR 1.02, 95% CI 0.85–1.24) were not associated with prostate cancer death, without dose dependency.ConclusionStatin use after initiation of ADT, but not before, was associated with improved prostate cancer prognosis.

Highlights

  • Statins reduce blood cholesterol levels, which play a central role in androgen biosynthesis

  • Statin use before androgen deprivation therapy (ADT) initiation was not associated with prostate cancer-specific survival (HR 1.12; 0.95 confidence intervals (CI) 0.96–1.31) (Table 2)

  • We have shown in a cohort of FinRSPC PCa patients that statin use after initiation of ADT, but not before, is associated with improved prostate cancer survival

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Summary

Introduction

Statins reduce blood cholesterol levels, which play a central role in androgen biosynthesis. The immune response against tumors provides another possible mechanism for statins’ anti-cancer effects [3]. Statin use has been associated with a longer time to disease progression after the primary therapy [1, 4, 5] and reduced disease-specific mortality [6]. Intraprostatic cholesterol metabolism and its upregulation have a key role in the development of castration-resistance during androgen deprivation therapy (ADT) [7]. There are only a few studies assessing statins’ effect in relation to ADT.

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