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培美曲塞为基础的化疗用于治疗具有20号外显子插入突变的非小细胞肺癌患者:一项多中心研究。

Pemetrexed-based chemotherapy for non-small-cell lung cancer patients with exon 20 insertion mutation: a multicenter study.

作者信息

Xu Chun-Wei, Wang Wen-Xian, Wang Dong, Wang Qi-Ming, Pu Xing-Xiang, Zhu You-Cai, Huang Jian-Hui, Yu Zong-Yang, Cui Zhao-Lei, Chen Xiao-Hui, Li Jin-Luan, Fang Yong, Wang Hong, Zhuang Wu, Lan Shi-Jie, Cai Xin, Zhang Yin-Bin, Gao Wen-Bin, Wang Li-Ping, She Ke-Lin, Rao Chuang-Zhou, Zhou Yue-Fen, Fang Mei-Yu, Miao Li-Yun, Lei Lei, Lv Tang-Feng, Song Yong

机构信息

Department of Respiratory Medicine, Affiliated Jinling Hospital, Medical School of Nanjing University, Nanjing, China.

Department of Medical Oncology, Chinese Academy of Sciences University Cancer Hospital (Zhejiang Cancer Hospital), Hangzhou China.

出版信息

Transl Lung Cancer Res. 2020 Oct;9(5):1853-1861. doi: 10.21037/tlcr-20-382.

Abstract

BACKGROUND

Chemotherapy is the major choice for advanced non-small-cell lung cancer (NSCLC) patients with epidermal growth factor receptor exon 20 insertion (EGFR ex20ins). The efficacy of pemetrexed-based with other chemotherapy regimens and EGFR ex20ins subtypes in this population has not been well studied.

METHODS

We screened patients with EGFR ex20ins by next-generation sequencing (NGS) from a large cohort. The clinicopathologic and medical information were collected in advanced NSCLC patients with EGFR ex20ins. We also compared the clinical outcomes among patients with different subtypes of EGFR ex20ins.

RESULTS

We retrospectively collected 119 stage IIIB/IV NSCLC patients with EGFR ex20ins from 9142 NSCLC patients across China from June 2013 to December 2018. The subtypes of EGFR ex20ins included A767_V769dupASV (33/119, 27.73%), S768_D770dupSVD (19/119, 15.97%), N771_H773dupNPH (11/119, 9.24%), A763_Y764insFQEA (2/119, 1.68%) and others (54/119, 45.38%). A total of 64.7% (77/119) of patients received pemetrexed-based first-line chemotherapy and 13.45% (16/119) of patients received pemetrexed-based second-line chemotherapy. Pemetrexed-based chemo-treated patients had longer median progression-free survival (PFS) than patients without pemetrexed-based chemo-treated (5.5 3.0 months, P=0.0026). Survival data was available for 66 patients and the median overall survival (OS) was 24.7 months. Pemetrexed-based chemo-treated patients had longer OS tendency than patients without pemetrexed-based chemo-treated (25.0 19.6 months, P=0.0769). Patients harboring A767_V769dupASV had better OS than other subtypes of EGFR ex20ins but without statistical significance (P=0.0676). Multivariate analysis revealed that histological type of NSCLC and bone-metastasis before treatment were independent prognostic factors for OS in all patients after adjusting all characteristic and treatment factors (P<0.05).

CONCLUSIONS

To the best of our knowledge, it is the largest cohort study of advanced NSCLC patients with EGFR ex20ins across China. Pemetrexed-based treatment could have better control of disease than non-pemetrexed-based chemotherapies in this population. Furthermore, more effective agents are expected for patients harboring EGFR ex20ins.

摘要

背景

化疗是晚期表皮生长因子受体第20外显子插入(EGFR ex20ins)的非小细胞肺癌(NSCLC)患者的主要治疗选择。培美曲塞联合其他化疗方案以及EGFR ex20ins亚型在该人群中的疗效尚未得到充分研究。

方法

我们通过下一代测序(NGS)从一个大型队列中筛选出EGFR ex20ins患者。收集晚期EGFR ex20ins NSCLC患者的临床病理和医疗信息。我们还比较了不同EGFR ex20ins亚型患者的临床结局。

结果

我们回顾性收集了2013年6月至2018年12月期间来自中国各地9142例NSCLC患者中的119例IIIB/IV期EGFR ex20ins NSCLC患者。EGFR ex20ins亚型包括A767_V769dupASV(33/119,27.73%)、S768_D770dupSVD(19/119,15.97%)、N771_H773dupNPH(11/119,9.24%)、A763_Y764insFQEA(2/119,1.68%)和其他(54/119,45.38%)。共有64.7%(77/119)的患者接受了以培美曲塞为基础的一线化疗,13.45%(16/119)的患者接受了以培美曲塞为基础的二线化疗。接受培美曲塞化疗的患者的中位无进展生存期(PFS)长于未接受培美曲塞化疗的患者(5.5对3.0个月,P = 0.0026)。66例患者有生存数据,中位总生存期(OS)为24.7个月。接受培美曲塞化疗的患者的OS有长于未接受培美曲塞化疗的患者的趋势(25.0对19.6个月,P = 0.0769)。携带A767_V769dupASV的患者的OS优于其他EGFR ex20ins亚型,但无统计学意义(P = 0.0676)。多因素分析显示,在调整所有特征和治疗因素后,NSCLC的组织学类型和治疗前的骨转移是所有患者OS的独立预后因素(P<0.05)。

结论

据我们所知,这是中国最大规模的晚期EGFR ex20ins NSCLC患者队列研究。在该人群中,以培美曲塞为基础的治疗比不以培美曲塞为基础的化疗能更好地控制疾病。此外,对于携带EGFR ex20ins的患者,预计会有更有效的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7672/7653161/efaa15d10cbf/tlcr-09-05-1853-f1.jpg

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