Lee Chung-Shien, Lam So Yi, Liu Angel, Sison Cristina, Zhu Xin-Hua
Department of Clinical Health Professions, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, USA.
Division of Medical Oncology and Hematology, Northwell Health Cancer Institute, Donald & Barbara Zucker School of Medicine at Hofstra/Northwell, Lake Success, NY, USA.
Clin Med Insights Oncol. 2023 Feb 1;17:11795549231152073. doi: 10.1177/11795549231152073. eCollection 2023.
Previous studies demonstrated that metformin could lead to an inhibition of proliferation of cancer cells through a shift from anabolic to catabolic metabolism. In this study, we seek to investigate the effect of metformin in metastatic prostate cancer.
Patients followed at Northwell Health Zuckerberg Cancer Center during 2014-2018 were included if they were diagnosed with metastatic hormone-sensitive prostate cancer (mHSPC) or metastatic castration-resistant prostate cancer (mCRPC), with ⩾6 months follow-up with and without metformin treatment. The primary outcomes, 6-month prostate-specific antigen (PSA) response, overall survival (OS), and radiographic progression free survival (rPFS), were evaluated.
There were 267 patients included in the final analysis; 196 patients had mHSPC (73.2%) and 71 had mCRPC (26.8%). Within the mHSPC subjects, there was a significant difference in OS between metformin vs nonmetformin groups (148.5 vs 85.6 months; < .046) in a univariate analysis; patients who took metformin had a significantly longer OS than subjects who did not (median OS: 148.5 vs 86 months; < .046). There was no significant difference between the 2 groups with respect to either PSA response rate at 6 months or rPFS or OS in patients with mHSPC in both univariate and multivariate analysis. Within the mCRPC subjects, there was no significant difference between metformin and nonmetformin groups with respect to OS (43.3 vs 51.5 months; < 0.160) or PSA response at 6 months (38.5% vs 57.1%; p < 0.24); however, patients on metformin had a significantly shorter rPFS in both the univariate analysis (7.3 vs 17.4; < .0002) and in the multivariate analysis (HR = 2.52; 95% CI: 1.24m 5.11; < .0109).
Among patients with mHSPC, use of metformin was not significantly associated with improved OS in the multivariate analysis.
既往研究表明,二甲双胍可通过将合成代谢转变为分解代谢来抑制癌细胞增殖。在本研究中,我们旨在探究二甲双胍对转移性前列腺癌的影响。
纳入2014年至2018年在诺斯韦尔健康扎克伯格癌症中心随访的患者,这些患者被诊断为转移性激素敏感性前列腺癌(mHSPC)或转移性去势抵抗性前列腺癌(mCRPC),且接受或未接受二甲双胍治疗并随访至少6个月。评估主要结局,即6个月前列腺特异性抗原(PSA)反应、总生存期(OS)和影像学无进展生存期(rPFS)。
最终分析纳入267例患者;196例为mHSPC(73.2%),71例为mCRPC(26.8%)。在mHSPC患者中,单因素分析显示二甲双胍组与非二甲双胍组的OS存在显著差异(148.5个月对85.6个月;P<0.046);服用二甲双胍的患者OS显著长于未服用者(中位OS:148.5个月对86个月;P<0.046)。在单因素和多因素分析中,mHSPC患者的6个月PSA反应率、rPFS或OS在两组之间均无显著差异。在mCRPC患者中,二甲双胍组与非二甲双胍组在OS(43.3个月对51.5个月;P<0.