Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy.
Unit of Thoracic Oncology, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Clin Lung Cancer. 2019 May;20(3):e413-e417. doi: 10.1016/j.cllc.2018.12.011. Epub 2018 Dec 19.
Advanced lung adenocarcinoma with inactive liver kinase B1 (LKB1) tumor suppressor protein is associated with poor response to immune checkpoint inhibitors and molecularly targeted agents, and with dismal patient prognosis. LKB1 is a central orchestrator of cancer cell metabolism, and halts tumor growth/proliferation during metabolic stress. Recent preclinical evidence suggests that LKB1-inactive lung adenocarcinoma is highly sensitive to metformin, a safe and low-cost antidiabetic compound that inhibits mitochondrial oxidative phosphorylation. The effects of metformin can be enhanced by nutrient deprivation (ie, glucose, amino acids), which reduces intracellular levels of ATP and anabolic precursors and can be achieved by the fasting mimicking diet (FMD). Noticeably, metformin also prevents resistance to cisplatin in preclinical in vitro and in vivo models of LKB1-inactive lung adenocarcinoma. Based on such preclinical evidence, the phase II FAME trial was designed to test the hypothesis that the addition of metformin, with or without cyclic FMD, to standard platinum-based chemotherapy improves the progression-free survival of patients with advanced, LKB-1 inactive lung adenocarcinoma. Enrolled patients will be randomized in a 1:1 ratio to receive cisplatin/carboplatin and pemetrexed with the addition of metformin alone (Arm A) or metformin plus FMD (Arm B). The FAME study will use a "pick-the-winner" design with the aim of establishing which of the 2 experimental treatments is superior in terms of antitumor efficacy and safety. The primary assumption of the study is that the combination of the 2 experimental treatments shall improve median progression-free survival from 7.6 months (historical data with chemotherapy alone) to 12 months. Secondary study endpoints are: objective response rate, overall survival, treatment tolerability, and compliance to the experimental treatment.
晚期肺腺癌中 LKB1(肝激酶 B1)肿瘤抑制蛋白失活与免疫检查点抑制剂和分子靶向药物反应差、患者预后差有关。LKB1 是癌细胞代谢的核心调节者,在代谢应激时可阻止肿瘤生长/增殖。最近的临床前证据表明,LKB1 失活的肺腺癌对二甲双胍高度敏感,二甲双胍是一种安全且廉价的抗糖尿病化合物,可抑制线粒体氧化磷酸化。二甲双胍可通过营养剥夺(即葡萄糖、氨基酸)增强其作用,这会降低细胞内 ATP 和合成前体的水平,而禁食模拟饮食(FMD)可实现这一点。值得注意的是,二甲双胍还可防止 LKB1 失活肺腺癌的临床前体外和体内模型中对顺铂产生耐药性。基于这些临床前证据,设计了 II 期 FAME 试验以检验以下假设:二甲双胍联合或不联合周期性 FMD 添加到标准铂类化疗中可改善晚期 LKB1 失活肺腺癌患者的无进展生存期。入组患者将以 1:1 的比例随机分为两组,分别接受顺铂/卡铂和培美曲塞联合或不联合二甲双胍(A 组)或二甲双胍加 FMD(B 组)。FAME 研究将采用“胜者为王”设计,旨在确定两种实验性治疗中哪种在抗肿瘤疗效和安全性方面更具优势。该研究的主要假设是,两种实验性治疗的联合应用可将中位无进展生存期从 7.6 个月(单独化疗的历史数据)延长至 12 个月。次要研究终点为:客观缓解率、总生存期、治疗耐受性和对实验性治疗的依从性。