Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Med Oncol. 2023 Jun 1;40(7):192. doi: 10.1007/s12032-023-02057-y.
Immune checkpoint inhibitors (ICIs) ± chemotherapy is the standard treatment for driver mutation-negative non-small cell lung cancer (NSCLC). However, accessibility to ICIs in LMICs is limited due to high cost, and platinum-based chemotherapy remains the mainstay of treatment. Metformin has anticancer properties, and studies suggest synergism between metformin and pemetrexed. Based on preclinical evidence, this combination may be more beneficial for STK11-mutated NSCLC, a subgroup, inherently resistant to ICIs. In this Simon two-stage, single-arm phase 2 trial, we investigated metformin with pemetrexed-carboplatin (PC) in patients with treatment-naive stage IV non-squamous NSCLC. The primary outcome was 6-month progression-free survival (PFS) rate. Secondary outcomes were safety, overall survival (OS), overall response rate (ORR), proportion of STK11 mutation, and effect of STK11 mutation on 6-month PFS rate. The study was terminated for futility after interim analysis. The median follow-up was 34.1 months. The 6-month PFS rate was 28% (95% CI 12.4-0.46). The median PFS and OS were 4.5 (95% CI 2.2-6.1) and 7.4 months (95% CI 5.3-15.3), respectively. The ORR was 72%. Gastrointestinal toxicities were the most common. No grade 4/5 toxicities were reported. Targeted sequencing was possible in nine cases. Two patients had STK11 mutation and a poor outcome (PFS < 12 weeks). We could not demonstrate the benefit of metformin with CP in terms of improvement in 6-month PFS rate; however, the combination was safe (CTRI/2019/02/017815).
免疫检查点抑制剂(ICIs)±化疗是驱动基因突变阴性非小细胞肺癌(NSCLC)的标准治疗方法。然而,由于成本高,免疫检查点抑制剂在中低收入国家的可及性有限,铂类化疗仍然是治疗的主要方法。二甲双胍具有抗癌特性,研究表明二甲双胍与培美曲塞具有协同作用。基于临床前证据,这种联合治疗可能对 STK11 突变的 NSCLC 更有益,这是一个对 ICI 固有耐药的亚组。在这项 Simon 两阶段、单臂 2 期临床试验中,我们研究了二甲双胍联合培美曲塞-卡铂(PC)在未经治疗的 IV 期非鳞状 NSCLC 患者中的应用。主要结局是 6 个月无进展生存率(PFS)。次要结局包括安全性、总生存期(OS)、总缓解率(ORR)、STK11 突变比例以及 STK11 突变对 6 个月 PFS 率的影响。中期分析后,该研究因无效而终止。中位随访时间为 34.1 个月。6 个月 PFS 率为 28%(95%CI 12.4-0.46)。中位 PFS 和 OS 分别为 4.5 个月(95%CI 2.2-6.1)和 7.4 个月(95%CI 5.3-15.3)。ORR 为 72%。胃肠道毒性是最常见的毒性。未报告 4/5 级毒性。九例可进行靶向测序。两名患者有 STK11 突变,预后不良(PFS<12 周)。我们不能证明 CP 联合二甲双胍在改善 6 个月 PFS 率方面的获益,但该联合方案是安全的(CTRI/2019/02/017815)。