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二甲双胍作为晚期非小细胞肺癌(NSCLC)的再利用治疗方法:一项 II 期试验的结果。

Metformin as a repurposed therapy in advanced non-small cell lung cancer (NSCLC): results of a phase II trial.

机构信息

Mount Sinai Health System, Icahn School of Medicine, Mount Sinai Downtown- Chelsea Cancer Center, 325 W. 15th St, New York, NY, 10011, USA.

Manhattan Veterans Association Hospital, NYU Langone Perlmutter Cancer Center, New York, NY, USA.

出版信息

Invest New Drugs. 2017 Dec;35(6):813-819. doi: 10.1007/s10637-017-0511-7. Epub 2017 Sep 22.

Abstract

Background Metformin has been shown to have anti-neoplastic activity in non-small cell lung cancer (NSCLC) in both preclinical and observational studies, however this has never been prospectively evaluated. This single-arm phase II trial, while not fully accrued, is the first known prospective study evaluating the use of metformin with chemotherapy in advanced NSCLC. Methods Patients received carboplatin AUC 5 + pemetrexed 500 mg/m2 IV every 21 days for 4 cycles. For patients who achieved at least stable disease, maintenance pemetrexed was administered until progression or toxicity. Metformin was initiated at 1000 mg/day for week 1, 1500 mg/day for week 2, then 2000 mg/day thereafter, in divided doses. The primary endpoint was progression-free survival (PFS). Secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), duration of response (DOR), and adverse events (AE). Tumor tissue was tested for LKB1/STK11 mutations, and non-fasting serum insulin levels were longitudinally assessed. Results Of a planned 50 patients, 14 were enrolled. ORR was 23% and median PFS was 3.9 months. Median OS was 11.7 months. No LKB1/STK11 mutations were identified. The most common AE were fatigue (42.9%), anemia, and nausea (28.6% each). The most common grade III AE was nausea (14.3%). No grade IV AE occurred. Mean duration of metformin treatment was 5.6 months. Conclusion Adding metformin to chemotherapy for advanced NSCLC was safe but did not significantly improve clinical outcomes compared to historical phase III controls. These results are limited by the small sample size; larger trials are needed.

摘要

背景

在非小细胞肺癌(NSCLC)的临床前和观察性研究中,二甲双胍已显示出抗肿瘤活性,但尚未进行前瞻性评估。这项单臂 II 期试验,虽然尚未完全入组,但却是首个已知的前瞻性研究,评估了二甲双胍联合化疗治疗晚期 NSCLC 的疗效。

方法

患者接受卡铂 AUC 5+培美曲塞 500mg/m2 静脉注射,每 21 天为一个周期,共 4 个周期。对于至少达到稳定疾病的患者,给予培美曲塞维持治疗,直到疾病进展或出现毒性。二甲双胍起始剂量为 1000mg/天,第 1 周;1500mg/天,第 2 周;然后,此后每天 2000mg,分剂量服用。主要终点是无进展生存期(PFS)。次要终点是总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)、缓解持续时间(DOR)和不良事件(AE)。检测肿瘤组织的 LKB1/STK11 突变,以及非禁食血清胰岛素水平进行纵向评估。

结果

计划入组 50 例患者,入组 14 例。ORR 为 23%,中位 PFS 为 3.9 个月。中位 OS 为 11.7 个月。未发现 LKB1/STK11 突变。最常见的 AE 为疲劳(42.9%)、贫血和恶心(各 28.6%)。最常见的 III 级 AE 为恶心(14.3%)。未发生 IV 级 AE。二甲双胍治疗的平均持续时间为 5.6 个月。

结论

在晚期 NSCLC 患者中,化疗联合二甲双胍治疗是安全的,但与历史 III 期对照相比,并未显著改善临床结局。这些结果受到样本量小的限制,需要更大规模的试验。

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