Department of Oncology, Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, Maryland.
Division of Biostatistics and Bioinformatics, Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, Maryland.
Oncologist. 2018 Jul;23(7):859-865. doi: 10.1634/theoncologist.2017-0465. Epub 2018 Feb 27.
In the absence of a targeted oncogenic driver mutation or high programmed death-ligand 1 expression, systemic therapy with platinum-based doublet chemotherapy with or without bevacizumab has been the standard treatment in advanced or metastatic non-small cell lung cancer (NSCLC). Metformin has been shown to have antitumor effects via a variety of insulin-dependent and insulin-independent mechanisms and to be potentially synergistic with chemotherapy.
This open-label single-center phase II study (NCT01578551) enrolled patients with chemotherapy-naïve advanced or metastatic nonsquamous NSCLC and randomized them (3:1) to receive carboplatin, paclitaxel, and bevacizumab with (Arm A) or without (Arm B) concurrent metformin for four to six cycles followed by maintenance therapy with bevacizumab ± metformin continued until disease progression, intolerable toxicity, or study withdrawal. The primary outcome was 1-year progression free survival (PFS). Secondary outcomes included overall survival, response to therapy, and toxicity.
A total of 25 patients were enrolled from August 2012 to April 2015, of whom 24 received at least one cycle of therapy administration. The study was stopped early due to slow accrual and changes in standard first-line therapy of advanced NSCLC. The 1-year PFS on Arm A ( = 18) was 47% (95% confidence interval [CI]: 25%-88%), which exceeded the historical control 1-year PFS of 15%. Median overall survival of patients treated on Arm A was 15.9 months (95% CI: 8.4-not available [NA]) and 13.9 months (95% CI: 12.7-NA) on Arm B. There were no significant differences in toxicity between the study arms.
To the authors' knowledge, this is the first study to show a significant benefit in PFS with the use of metformin in this patient population and is a signal of efficacy for metformin in advanced NSCLC.
The anticancer effects of metformin continue to be elucidated. To the authors' knowledge, this is the first trial in nondiabetic advanced non-small cell lung cancer patients to show a significant change in outcome with the addition of metformin to standard first-line chemotherapy. Well tolerated and widely available, metformin is a drug that should be considered for further study in the lung cancer treatment landscape.
在缺乏靶向致癌驱动突变或高程序性死亡配体 1 表达的情况下,含铂双药化疗联合或不联合贝伐珠单抗的全身治疗一直是晚期或转移性非小细胞肺癌(NSCLC)的标准治疗方法。二甲双胍已通过多种胰岛素依赖和胰岛素非依赖机制显示出抗肿瘤作用,并可能与化疗具有协同作用。
这项开放标签的单中心 II 期研究(NCT01578551)纳入了化疗初治的晚期或转移性非鳞状 NSCLC 患者,并将其随机(3:1)分为接受卡铂、紫杉醇和贝伐珠单抗联合(A 组)或不联合(B 组)二甲双胍治疗 4-6 个周期,随后接受贝伐珠单抗联合或不联合二甲双胍维持治疗,直至疾病进展、无法耐受毒性或研究退出。主要终点为 1 年无进展生存期(PFS)。次要终点包括总生存期、治疗反应和毒性。
共有 25 例患者于 2012 年 8 月至 2015 年 4 月入组,其中 24 例至少接受了一个周期的治疗。由于进展缓慢和晚期 NSCLC 标准一线治疗的变化,该研究提前终止。A 组(n=18)的 1 年 PFS 为 47%(95%置信区间 [CI]:25%-88%),超过了历史对照的 1 年 PFS(15%)。A 组患者的中位总生存期为 15.9 个月(95%CI:8.4-未获得[NA]),B 组为 13.9 个月(95%CI:12.7-NA)。两组之间的毒性无显著差异。
据作者所知,这是第一项表明在该患者人群中使用二甲双胍可显著改善 PFS 的研究,这也是二甲双胍在晚期 NSCLC 中的疗效信号。
二甲双胍的抗癌作用仍在阐明中。据作者所知,这是第一项在非糖尿病晚期非小细胞肺癌患者中进行的试验,表明添加二甲双胍到标准一线化疗可显著改变结局。二甲双胍耐受性良好且广泛可用,应该考虑将其用于进一步研究 NSCLC 的治疗。