TY - JOUR
T1 - Metformin Use and Outcome of Sunitinib Treatment in Patients With Diabetes and Metastatic Renal Cell Carcinoma
AU - Keizman, Daniel
AU - Ish-Shalom, Maya
AU - Sella, Avishay
AU - Gottfried, Maya
AU - Maimon, Natalie
AU - Peer, Avivit
AU - Hammers, Hans
AU - Eisenberger, Mario A.
AU - Sinibaldi, Victoria
AU - Neiman, Victoria
AU - Rosenbaum, Eli
AU - Sarid, David
AU - Mermershtain, Wilmosh
AU - Rouvinov, Keren
AU - Berger, Raanan
AU - Carducci, Michael A.
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - We analyzed the effect of metformin use on sunitinib treatment outcome in diabetic patients with metastatic renal cell carcinoma. In metformin users versus nonusers, clinical benefit was 96% versus 84% (P = .054), median progression-free survival was 15 versus 11.5 months (P = .1), and median overall survival (OS) was 32 versus 21 months (P = .001). In multivariate analyses of the entire patient cohort, metformin use was associated with OS. Background Although studies in several cancer types suggest that metformin has antitumor activity, its effect on the outcome of targeted therapies in metastatic renal cell carcinoma (mRCC) is poorly defined. We aimed to analyze the effect of metformin use on the outcome of sunitinib treatment in diabetic patients with mRCC. Patients and Methods We performed a retrospective study of diabetic patients with mRCC, who were treated with sunitinib in 8 centers across 2 countries. Patients were divided into metformin users and nonusers. The effect of metformin use on response rate, progression-free survival (PFS), and overall survival (OS), was tested. Furthermore, univariate and multivariate analyses of the association between clinicopathologic factors and metformin use, and outcome were performed using the entire patient cohort. Results Between 2004 and 2014, 108 diabetic patients with mRCC were treated with sunitinib. There were 52 metformin users (group 1) and 56 nonusers (group 2). The groups were balanced regarding clinicopathologic factors. Clinical benefit (partial response + stable disease) in group 1 versus 2 was 96% versus 84% (P = .054). Median PFS was 15 versus 11.5 months (P = .1). Median OS was 32 versus 21 months (P = .001). In multivariate analyses of the entire patient cohort (n = 108), factors associated with PFS were active smoking and pretreatment neutrophil to lymphocyte ratio > 3. Factors associated with OS were metformin use (hazard ratio, 0.21; P < .0001), Heng risk, active smoking, liver metastases, and pretreatment neutrophil to lymphocyte ratio > 3. Conclusion Metformin might improve the OS of diabetic patients with mRCC who are treated with sunitinib.
AB - We analyzed the effect of metformin use on sunitinib treatment outcome in diabetic patients with metastatic renal cell carcinoma. In metformin users versus nonusers, clinical benefit was 96% versus 84% (P = .054), median progression-free survival was 15 versus 11.5 months (P = .1), and median overall survival (OS) was 32 versus 21 months (P = .001). In multivariate analyses of the entire patient cohort, metformin use was associated with OS. Background Although studies in several cancer types suggest that metformin has antitumor activity, its effect on the outcome of targeted therapies in metastatic renal cell carcinoma (mRCC) is poorly defined. We aimed to analyze the effect of metformin use on the outcome of sunitinib treatment in diabetic patients with mRCC. Patients and Methods We performed a retrospective study of diabetic patients with mRCC, who were treated with sunitinib in 8 centers across 2 countries. Patients were divided into metformin users and nonusers. The effect of metformin use on response rate, progression-free survival (PFS), and overall survival (OS), was tested. Furthermore, univariate and multivariate analyses of the association between clinicopathologic factors and metformin use, and outcome were performed using the entire patient cohort. Results Between 2004 and 2014, 108 diabetic patients with mRCC were treated with sunitinib. There were 52 metformin users (group 1) and 56 nonusers (group 2). The groups were balanced regarding clinicopathologic factors. Clinical benefit (partial response + stable disease) in group 1 versus 2 was 96% versus 84% (P = .054). Median PFS was 15 versus 11.5 months (P = .1). Median OS was 32 versus 21 months (P = .001). In multivariate analyses of the entire patient cohort (n = 108), factors associated with PFS were active smoking and pretreatment neutrophil to lymphocyte ratio > 3. Factors associated with OS were metformin use (hazard ratio, 0.21; P < .0001), Heng risk, active smoking, liver metastases, and pretreatment neutrophil to lymphocyte ratio > 3. Conclusion Metformin might improve the OS of diabetic patients with mRCC who are treated with sunitinib.
KW - Metastatic Renal Cell Carcinoma
KW - Metformin
KW - Outcome
KW - Sunitinib
UR - http://www.scopus.com/inward/record.url?scp=84969211094&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2016.04.012
DO - 10.1016/j.clgc.2016.04.012
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C2 - 27211307
AN - SCOPUS:84969211094
SN - 1558-7673
VL - 14
SP - 420
EP - 425
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 5
ER -