Statin use is reportedly associated with the risk of prostate cancer, outcomes after treatment, and prostate cancer-specific mortality. We sought to determine the efficacy of adjuvant atorvastatin in prostate cancer after radical prostatectomy.
Experimental Design:In this randomized, double-blind trial, we assigned patients with pathologic high-risk prostate cancer to receive either low-dose atorvastatin (20 mg per day, n=183) or placebo (n=181) for 1 year after radical prostatectomy. The primary end point was the 1-year biochemical recurrence rate. The secondary end points included the 5-year biochemical recurrence-free survival and changes in lipid, testosterone and sex hormonebinding globulin levels.Results: From October 2012 through January 2019, a total of 364 patients underwent randomization. Among 59 total primary end points, 30 (16.4%) and 29 (16.0%) occurred in the atorvastatin and placebo groups, respectively. Atorvastatin did not significantly reduce the primary end point of 1-year biochemical recurrence (HR, 0.96; 95% CI, 0.58-1.60). During a median follow-up of 24 months, 131 patients experienced biochemical recurrence (68 in the atorvastatin group and 63 in the placebo group), representing Kaplan-Meier estimated event rates of 24.0% and 25.4% in the atorvastatin and placebo groups, respectively, at 24 months (HR, 1.00; 95% CI, 0.71-1.41). We observed no significant between-group differences in the testosterone and sex hormone-binding globulin levels.Conclusions: Among patients with high-risk pathologic features after radical prostatectomy for prostate cancer, 1-year adjuvant use of atorvastatin was not associated with a lower risk of disease recurrence compared to that for placebo. (Funded by Dong-A Pharmaceuticals; ClinicalTrials.gov number, NCT01759836)Research.