Statin and Metformin Use Prolongs Survival in Patients With Resectable Pancreatic Cancer. Issue 1 (January 2016)

• Record Type: Journal Article
• Authors: Kozak, Margaret M.; Anderson, Eric M.; von Eyben, Rie; Pai, Jonathan S.; Poultsides, George A.; Visser, Brendan C.; Norton, Jeffrey A.; Koong, Albert C.; Chang, Daniel T.
• Is Part Of: Pancreas. Volume 45:Issue 1(2016)
• Publication Date: 2016-01
• Subjects: statin -- metformin -- pancreatic cancer -- survival; Pancreas -- Diseases -- Periodicals; Pancreas -- Periodicals; Neuroendocrine tumors -- Periodicals; 616.37005
• DOI: 10.1097/MPA.0000000000000470
• Languages: English
• ISSNs: 0885-3177

Abstract

Abstract : Objectives: The aim of this study was to investigate the impact of statin and metformin therapy on disease outcome for patients with pancreatic ductal adenocarcinoma (PDAC). Methods: This retrospective study included 171 PDAC patients who underwent surgical resection at the Stanford Cancer Institute between 1998 and 2013. No patients received neoadjuvant therapy. Statin and metformin use was defined as use during initial consult and continuing upon discharge from the hospital after surgery. Dose of each medication was recorded, as was the type of statin taken. Results: The median follow-up for all patients was 11.23 months (range, 0.2–105.0 months). Among the 171 patients included in our analysis, 18 patients (10.5%) took metformin and 34 patients (19.9%) took statins. Statin use was associated with better overall survival (OS) in patients with PDAC ( P = 0.011). Metformin use was also associated with better OS ( P = 0.035). The use of statins remained significant on multivariate analysis for OS ( P = 0.014; hazards ratio, 0.33; 95% confidence interval, 0.139–0.799), but metformin use did not ( P = 0.33; hazards ratio 0.60, 95% confidence interval, 0.211–1.675). Conclusions: Statin and metformin use is associated with improved OS in patients with resectable PDAC. These medications should be further investigated for possible long-term use in the general population.