Abstract
Purpose: The 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors (statins) have activity in one of the pathways influenced by nitrogen-containing bisphosphonates, which are associated with improved survival in multiple myeloma (MM). To understand the benefit of statins in MM, we evaluated the association between statin use and mortality in a large cohort of patients with MM. Patients and Methods: From the Veterans Administration Central Cancer Registry, we identified patients diagnosed with MM between 1999 and 2013. We defined statin use as the presence of any prescription for a statin within 3 months before or any time after MM diagnosis. Cox proportional hazards regression assessed the association of statin use with mortality, while controlling for known MM prognostic factors. Results: We identified a cohort of 4,957 patients, of whom 2,294 received statin therapy. Statin use was associated with a 21% decrease in all-cause mortality (adjusted hazard ratio, 0.79; 95% CI, 0.73 to 0.86; P < .001) as well as a 24% decrease in MM-specific mortality (adjusted hazard ratio, 0.76; 95% CI, 0.67 to 0.86; P < .001). This association remained significant across all sensitivity analyses. In addition to reductions in mortality, statin use was associated with a 31% decreased risk of developing a skeletal-related event. Conclusion: In this cohort study of US veterans with MM, statin therapy was associated with a reduced risk of both all-cause and MM-specific mortality. Our findings suggest a potential role for statin therapy in patients with MM. The putative benefit of statin therapy in MM should be corroborated in prospective studies.
Original language | English (US) |
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Pages (from-to) | 4008-4014 |
Number of pages | 7 |
Journal | Journal of Clinical Oncology |
Volume | 34 |
Issue number | 33 |
DOIs | |
State | Published - Nov 20 2016 |
Funding
Supported by National Institutes of Health, National Heart, Lung, and Blood Institute Grants No. 5K12HL087107 and U54 HL112303; the Barnes Jewish Foundation; and the American Cancer Society Institutional Research Grant No. 58-010-52. Millennium, Kyowa Hakko Kirin, Allos Therapeutics, Celgene, Bristol-Myers Squibb, Seattle Genetics
ASJC Scopus subject areas
- Oncology
- Cancer Research