Low BMI patients with advanced EGFR mutation-positive NSCLC can get a better outcome from metformin plus EGFR-TKI as first-line therapy: A secondary analysis of a phase 2 randomized clinical trial

Rui Han , Jianghua Li , Yubo Wang, Tingting He, Jie Zheng, Yong He
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Abstract

Background

The synergistic association between metformin and epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) has been confirmed in in vitro studies. It is still controversial which patients can benefit from metformin plus EGFR-TKIs treatment. Body mass index (BMI) was proved to be independently associated with prolonged progression-free survival (PFS) and overall survival (OS). This study aimed to investigate whether BMI is associated with the synergistic effect of metformin and EGFR-TKIs in advanced EGFR mutation (EGFRm)-positive non-small cell lung cancer (NSCLC) among nondiabetic Asian population.

Methods

We performed a post hoc analysis of a prospective, double-blind phase II randomized clinical trial (COAST, NCT01864681), which enrolled 224 patients without diabetes with treatment-naïve stage IIIB-IV EGFRm NSCLC. We stratified patients into those with a high BMI (≥24 kg/m2) and those with a low BMI (<24 kg/m2) to allow an analysis of the difference in PFS and OS between the two groups. The PFS and OS were analyzed using Kaplan–Meier curves, and the differences between groups were compared using log-rank test.

Results

In the univariate analysis, patients who had a high BMI (n = 56) in the gefitinib + metformin group (n = 28) did not have a better PFS (8.84 months vs. 11.67 months; P = 0.351) or OS (15.58 months vs. 24.36 months; P = 0.095) than those in the gefitinib + placebo group (n = 28). Similar results were also observed in the low-BMI groups. Strikingly, in the metformin plus gefitinib group, patients who had low BMI (n = 69) showed significantly better OS than those with high BMI (24.89 months [95% CI, 20.68 months–not reached] vs. 15.58 months [95% CI, 13.78–31.53 months]; P = 0.007), but this difference was not observed in PFS (10.78 months vs. 8.84 months; P = 0.285).

Conclusions

Our study showed that nondiabetic Asian advanced NSCLC patients with EGFR mutations who have low BMI seem to get better OS from metformin plus EGFR-TKI treatment.

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低BMI晚期EGFR突变阳性NSCLC患者采用二甲双胍联合EGFR- tki作为一线治疗可以获得更好的结果:一项2期随机临床试验的二次分析
背景二甲双胍与表皮生长因子受体酪氨酸激酶抑制剂(TKIs)的协同作用已在体外研究中得到证实。哪些患者可以从二甲双胍加EGFR-TKIs治疗中获益仍存在争议。体重指数(BMI)被证明与延长的无进展生存期(PFS)和总生存期(OS)独立相关。本研究旨在研究在非糖尿病亚洲人群中,BMI是否与二甲双胍和EGFR-TKI在晚期EGFR突变(EGFRm)阳性非小细胞肺癌癌症(NSCLC)中的协同作用有关。方法我们对一项前瞻性、双盲的II期随机临床试验(COAST,NCT01864681)进行了事后分析,该试验纳入了224名非糖尿病患者,他们接受了早期IIIB-IV期EGFRm NSCLC的治疗。我们将患者分为高BMI(≥24 kg/m2)和低BMI(<;24 kg/m2。使用Kaplan–Meier曲线分析PFS和OS,并使用对数秩检验比较各组之间的差异。结果在单因素分析中,服用吉非替尼的患者BMI较高(n=56) + 二甲双胍组(n=28)的PFS(8.84个月vs.11.67个月;P=0.351)或OS(15.58个月vs.24.36个月;P=0.095)均未优于吉非替尼组 + 安慰剂组(n=28)。在低BMI组中也观察到类似的结果。值得注意的是,在二甲双胍加吉非替尼组中,低BMI患者(n=69)的OS明显好于高BMI患者(24.89个月[95%CI,20.68个月–未达到]对15.58个月[95%CI,13.78-11.53个月];P=0.007),但在PFS中没有观察到这种差异(10.78个月对8.84个月;P=0.285)。结论我们的研究表明,患有EGFR突变且BMI较低的非糖尿病亚洲晚期NSCLC患者似乎通过二甲双胍加EGFR-TKI治疗获得了更好的OS。
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来源期刊
Chinese medical journal pulmonary and critical care medicine
Chinese medical journal pulmonary and critical care medicine Critical Care and Intensive Care Medicine, Infectious Diseases, Pulmonary and Respiratory Medicine
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