TY - JOUR
T1 - Effect of Metformin Use on Survival Outcomes in Patients With Metastatic Renal Cell Carcinoma
AU - Hamieh, Lana
AU - McKay, Rana R.
AU - Lin, Xun
AU - Moreira, Raphael B.
AU - Simantov, Ronit
AU - Choueiri, Toni K.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - In light of the emerging evidence of the antineoplastic potential of metformin, we investigated its effect on survival outcomes in metastatic renal cell carcinoma using a large clinical trial database. Although metformin did not affect survival in the overall cohort, it conferred a survival advantage in diabetic metastatic renal cell carcinoma patients treated with sunitinib. Introduction Observational studies have suggested that metformin use is associated with favorable outcomes in several cancers. For renal cell carcinoma (RCC), data have been limited. Therefore, we investigated the effect of metformin on survival in metastatic RCC (mRCC) using a large clinical trial database. Patients and Methods We conducted a retrospective analysis of patients with mRCC in phase II and III clinical trials. The overall survival (OS) in metformin users was compared with that of users of other antidiabetic agents and those not using antidiabetic agents. Progression-free survival, objective response rate, and adverse events were secondary endpoints. Subgroup analyses were conducted after stratifying by class of therapy, type of vascular endothelial growth factor tyrosine kinase inhibitors, and International Metastatic RCC Database Consortium (IMDC) risk groups. Results We identified 4736 patients with mRCC, including 486 with diabetes, of whom 218 (4.6%) were taking metformin. Metformin use did not affect OS when compared with users of other antidiabetic agents or those without diabetes. Furthermore, metformin use did not confer an OS advantage when stratified by class of therapy and IMDC risk group. However, in diabetic patients receiving sunitinib (n = 128), metformin use was associated with an improvement in OS compared with users of other antidiabetic agents (29.3 vs. 20.9 months, respectively; hazard ratio, 0.051; 95% confidence interval, 0.009-0.292; P = .0008). Conclusion In the present study, we found a survival benefit for metformin use in mRCC patients treated with sunitinib. Clinical and preclinical studies are warranted to validate our results and guide the use of metformin in the clinic.
AB - In light of the emerging evidence of the antineoplastic potential of metformin, we investigated its effect on survival outcomes in metastatic renal cell carcinoma using a large clinical trial database. Although metformin did not affect survival in the overall cohort, it conferred a survival advantage in diabetic metastatic renal cell carcinoma patients treated with sunitinib. Introduction Observational studies have suggested that metformin use is associated with favorable outcomes in several cancers. For renal cell carcinoma (RCC), data have been limited. Therefore, we investigated the effect of metformin on survival in metastatic RCC (mRCC) using a large clinical trial database. Patients and Methods We conducted a retrospective analysis of patients with mRCC in phase II and III clinical trials. The overall survival (OS) in metformin users was compared with that of users of other antidiabetic agents and those not using antidiabetic agents. Progression-free survival, objective response rate, and adverse events were secondary endpoints. Subgroup analyses were conducted after stratifying by class of therapy, type of vascular endothelial growth factor tyrosine kinase inhibitors, and International Metastatic RCC Database Consortium (IMDC) risk groups. Results We identified 4736 patients with mRCC, including 486 with diabetes, of whom 218 (4.6%) were taking metformin. Metformin use did not affect OS when compared with users of other antidiabetic agents or those without diabetes. Furthermore, metformin use did not confer an OS advantage when stratified by class of therapy and IMDC risk group. However, in diabetic patients receiving sunitinib (n = 128), metformin use was associated with an improvement in OS compared with users of other antidiabetic agents (29.3 vs. 20.9 months, respectively; hazard ratio, 0.051; 95% confidence interval, 0.009-0.292; P = .0008). Conclusion In the present study, we found a survival benefit for metformin use in mRCC patients treated with sunitinib. Clinical and preclinical studies are warranted to validate our results and guide the use of metformin in the clinic.
KW - Diabetes
KW - Kidney cancer
KW - Prognosis
KW - Sunitinib
KW - Targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85008395898&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2016.06.017
DO - 10.1016/j.clgc.2016.06.017
M3 - Article
C2 - 27460432
AN - SCOPUS:85008395898
SN - 1558-7673
VL - 15
SP - 221
EP - 229
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 2
ER -