Department of Thoracic Surgery, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
Department of Immunology, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
J Thorac Oncol. 2019 Dec;14(12):2181-2187. doi: 10.1016/j.jtho.2019.07.020. Epub 2019 Aug 6.
Metformin, a common medication used in the treatment of diabetes mellitus is known to have anticancer effects. We hypothesized that the salutary effect of metformin on the survival of patients with stage I NSCLC is influenced by body mass index (BMI).
Patients undergoing lobectomy for stage I NSCLC without neoadjuvant therapy were included. Univariate and multivariate survival analyses to examine the association between metformin use and overall survival (OS), disease-specific survival (DSS), and recurrence-free survival were performed, stratified by BMI (>25 kg/m and ≤25 kg/m). Expression of immune checkpoints in patients on metformin and not was performed in a separate cohort of 205 patients with advanced disease.
Four hundred thirty-four stage I patients (including 74 metformin users) were deemed eligible for analysis. Univariate and multivariate analysis revealed an association between metformin use and OS (hazard ratio [HR] = 0.52; p = 0.04) as well as DSS (HR = 0.21; p = 0.04) but not recurrence-free survival (HR = 0.67; p = 0.33) in high-BMI patients only. In a separate cohort of 205 patients with tumors of all stages (including 35 metformin users), downregulation of immune checkpoint gene expression (programmed cell death 1, cytotoxic T-lymphocyte associated protein 4, B and T lymphocyte associated, CD27 molecule, lymphocyte activating 3, and inducible T cell costimulator) in metformin users was seen only in high-BMI patients, with upregulation of these genes seen in low-BMI patients with metformin use.
Metformin use may be associated with better OS and DSS only in high-BMI patients. This hypothesis is supported by gene expression data of immune checkpoint genes in metformin users using a separate cohort of advanced-stage tumors. Further studies examining the interaction of BMI with metformin in NSCLC are worthwhile.
二甲双胍是一种常用于治疗糖尿病的常用药物,已知具有抗癌作用。我们假设二甲双胍对 I 期非小细胞肺癌(NSCLC)患者生存的有益影响受体重指数(BMI)的影响。
纳入未接受新辅助治疗而行肺叶切除术的 I 期 NSCLC 患者。进行单变量和多变量生存分析,以检查接受二甲双胍治疗的患者与总体生存率(OS)、疾病特异性生存率(DSS)和无复发生存率之间的关系,按 BMI(>25kg/m 和 ≤25kg/m)分层。在另一组 205 名晚期疾病患者中,对使用和不使用二甲双胍的患者进行了免疫检查点的表达分析。
434 名 I 期患者(包括 74 名二甲双胍使用者)被认为符合分析条件。单变量和多变量分析显示,在高 BMI 患者中,二甲双胍的使用与 OS(风险比 [HR] = 0.52;p = 0.04)和 DSS(HR = 0.21;p = 0.04)相关,但与无复发生存率(HR = 0.67;p = 0.33)无关。在另一组包括所有分期肿瘤的 205 名患者(包括 35 名二甲双胍使用者)中,仅在高 BMI 患者中观察到二甲双胍使用者的免疫检查点基因表达下调(程序性细胞死亡 1、细胞毒性 T 淋巴细胞相关蛋白 4、B 和 T 淋巴细胞相关、CD27 分子、淋巴细胞激活 3 和诱导型 T 细胞共刺激物),而低 BMI 患者使用二甲双胍时这些基因上调。
只有在高 BMI 患者中,二甲双胍的使用才可能与更好的 OS 和 DSS 相关。这一假设得到了使用另一组晚期肿瘤患者的免疫检查点基因的二甲双胍使用者的基因表达数据的支持。进一步研究检查 BMI 与 NSCLC 中二甲双胍的相互作用是值得的。