Arrieta Oscar, Barrón Feliciano, Padilla Miguel-Ángel Salinas, Avilés-Salas Alejandro, Ramírez-Tirado Laura Alejandra, Arguelles Jiménez Manuel Jesús, Vergara Edgar, Zatarain-Barrón Zyanya Lucia, Hernández-Pedro Norma, Cardona Andrés F, Cruz-Rico Graciela, Barrios-Bernal Pedro, Yamamoto Ramos Masao, Rosell Rafael
Thoracic Oncology Unit, Instituto Nacional de Cancerología (INCan), Mexico City, Mexico.
Clinical and Translational Oncology Group, Clínica del Country, Bogotá, Colombia.
JAMA Oncol. 2019 Nov 1;5(11):e192553. doi: 10.1001/jamaoncol.2019.2553. Epub 2019 Nov 14.
Metformin hydrochloride is emerging as a repurposed anticancer drug. Preclinical and retrospective studies have shown that it improves outcomes across a wide variety of neoplasms, including lung cancer. Particularly, evidence is accumulating regarding the synergistic association between metformin and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs).
To assess the progression-free survival (PFS) in patients with advanced lung adenocarcinoma who received treatment with EGFR-TKIs plus metformin compared with those who received EGFR-TKIs alone.
DESIGN, SETTING, AND PARTICIPANTS: Open-label, randomized, phase 2 trial conducted at the Instituto Nacional de Cancerología (INCan), Mexico City, Mexico. Eligible patients were 18 years or older, had histologically confirmed stage IIIB-IV lung adenocarcinoma with an activating EGFR mutation.
Patients were randomly allocated to receive EGFR-TKIs (erlotinib hydrochloride, afatinib dimaleate, or gefitinib at standard dosage) plus metformin hydrochloride (500 mg twice a day) or EGFR-TKIs alone. Treatment was continued until occurrence of intolerable toxic effects or withdrawal of consent.
The primary outcome was PFS in the intent-to-treat population. Secondary outcomes included objective response rate, disease control rate, overall survival (OS), and safety.
Between March 31, 2016, and December 31, 2017, a total of 139 patients (mean [SD] age, 59.4 [12.0] years; 65.5% female) were randomly assigned to receive EGFR-TKIs (n = 70) or EGFR-TKIs plus metformin (n = 69). The median PFS was significantly longer in the EGFR-TKIs plus metformin group (13.1; 95% CI, 9.8-16.3 months) compared with the EGFR-TKIs group (9.9; 95% CI, 7.5-12.2 months) (hazard ratio, 0.60; 95% CI, 0.40-0.94; P = .03). The median OS was also significantly longer for patients receiving the combination therapy (31.7; 95% CI, 20.5-42.8 vs 17.5; 95% CI, 11.4-23.7 months; P = .02).
To our knowledge, this is the first study to prospectively show that the addition of metformin to standard EGFR-TKIs therapy in patients with advanced lung adenocarcinoma significantly improves PFS. These results justify the design of a phase 3, placebo-controlled study.
ClinicalTrials.gov identifier: NCT03071705.
盐酸二甲双胍正作为一种重新利用的抗癌药物崭露头角。临床前和回顾性研究表明,它能改善包括肺癌在内的多种肿瘤的治疗效果。特别是,关于二甲双胍与表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKIs)之间协同关联的证据正在不断积累。
评估接受EGFR-TKIs联合二甲双胍治疗的晚期肺腺癌患者与仅接受EGFR-TKIs治疗的患者的无进展生存期(PFS)。
设计、地点和参与者:在墨西哥城的墨西哥国立癌症研究所(INCan)进行的开放标签、随机、2期试验。符合条件的患者年龄在18岁及以上,经组织学确诊为伴有EGFR激活突变的IIIB-IV期肺腺癌。
患者被随机分配接受EGFR-TKIs(盐酸厄洛替尼、马来酸阿法替尼或吉非替尼,标准剂量)联合盐酸二甲双胍(每日两次,每次500毫克)或仅接受EGFR-TKIs治疗。治疗持续至出现无法耐受的毒性作用或患者撤回同意。
主要结局是意向性治疗人群的PFS。次要结局包括客观缓解率、疾病控制率、总生存期(OS)和安全性。
在2016年3月31日至2017年12月31日期间,共有139例患者(平均[标准差]年龄为59.4[12.0]岁;65.5%为女性)被随机分配接受EGFR-TKIs治疗(n = 70)或EGFR-TKIs联合二甲双胍治疗(n = 69)。与EGFR-TKIs组(9.9;95%置信区间,7.5-12.2个月)相比,EGFR-TKIs联合二甲双胍组的中位PFS显著更长(13.1;95%置信区间,9.8-16.3个月)(风险比,0.60;95%置信区间,0.40-0.94;P = 0.03)。接受联合治疗的患者的中位OS也显著更长(31.7;95%置信区间,20.5-42.8对17.5;9%置信区间,11.4-23.7个月;P = 0.02)。
据我们所知,这是第一项前瞻性研究,表明在晚期肺腺癌患者的标准EGFR-TKIs治疗中添加二甲双胍可显著改善PFS。这些结果为开展一项3期、安慰剂对照研究提供了依据。
ClinicalTrials.gov标识符:NCT03071705。