Abstract

BackgroundPreclinical evidence suggests statins may have anti-tumor properties. Large observational studies are also consistent with improved survival and cancer-specific outcomes among cancer patients on statins. We sought to evaluate the randomized controlled trials of statins in addition to usual anti-cancer therapy.MethodsA systematic search of MEDLINE, Embase, CINAHL, Cochrane Library, Web of Science, Papers First and Clinicaltrials.gov was performed from inception through to July 4, 2017 to identify randomized clinical trials that investigated statin therapy in cancer patients. Our primary outcome was overall survival and our secondary outcome was progression-free survival. We calculated summary hazard ratio’s (HR) and 95% confidence intervals (CI) based on random-effects models using aggregate data. PROSPERO (CRD42017065503).ResultsTen studies with 1,881 individuals were included with 1,572 deaths and a median follow-up of 23 months. All trials included patients with advanced (stage 3 or higher) disease. There was minimal between-study statistical heterogeneity (I2 = 1.8%, for OS; I2 = 0%, for PFS). The pooled HR for overall survival in patients randomized to statins plus standard anti-cancer therapy versus standard therapy alone was 0.94 (95% CI, 0.85 to 1.04). In the 9 studies that reported progression-free survival (1,798 participants), the pooled HR for statin plus standard therapy versus standard therapy alone was 0.97 (95% CI, 0.87 to 1.07).ConclusionsIn patients with advanced cancer and a prognosis <2 years, the addition of statins to standard anti-cancer therapy does not appear to improve overall survival or progression-free survival. Future research should assess if cancer patients with better prognosis benefit from longer-term statin therapy.

Highlights

  • There is a strong experimental rationale to suggest statins may improve cancer-specific outcomes

  • The pooled hazard ratio (HR) for overall survival in patients randomized to statins plus standard anti-cancer therapy versus standard therapy alone was 0.94

  • In the 9 studies that reported progression-free survival (1,798 participants), the pooled HR for statin plus standard therapy versus standard therapy alone was 0.97

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Summary

Introduction

There is a strong experimental rationale to suggest statins may improve cancer-specific outcomes. Preclinical evidence indicates statins inhibit tumor growth and induce apoptosis in a number of tumor types [1,2,3,4]. Statins have been studied for their potential chemo-sensitising effects through impairment of the Ras family signalling [7]. Consistent with the in vitro effects of statins, their efficacy has been demonstrated in animal models of breast, colon, lung and hematological cancers [8,9,10,11]. Preclinical evidence suggests statins may have anti-tumor properties. Large observational studies are consistent with improved survival and cancer-specific outcomes among cancer patients on statins. We sought to evaluate the randomized controlled trials of statins in addition to usual anti-cancer therapy

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