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First- or second-generation epidermal growth factor receptor tyrosine kinase inhibitors in a large, real-world cohort of patients with non-small cell lung cancer.在一个大型真实世界非小细胞肺癌患者队列中使用第一代或第二代表皮生长因子受体酪氨酸激酶抑制剂。
Ther Adv Med Oncol. 2021 Jul 31;13:17588359211035710. doi: 10.1177/17588359211035710. eCollection 2021.
2
Co-Occurring Potentially Actionable Oncogenic Drivers in Non-Small Cell Lung Cancer.非小细胞肺癌中同时存在的潜在可操作致癌驱动因素
Front Oncol. 2021 Jun 16;11:665484. doi: 10.3389/fonc.2021.665484. eCollection 2021.
3
A multicenter cohort study of osimertinib compared with afatinib as first-line treatment for EGFR-mutated non-small-cell lung cancer from practical dataset: CJLSG1903.一项多中心队列研究:奥希替尼对比阿法替尼作为 EGFR 突变非小细胞肺癌一线治疗:CJLSG1903 研究。
ESMO Open. 2021 Jun;6(3):100115. doi: 10.1016/j.esmoop.2021.100115. Epub 2021 May 10.
4
Efficacy of Osimertinib Plus Bevacizumab vs Osimertinib in Patients With EGFR T790M-Mutated Non-Small Cell Lung Cancer Previously Treated With Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor: West Japan Oncology Group 8715L Phase 2 Randomized Clinical Trial.奥希替尼联合贝伐珠单抗对比奥希替尼用于既往接受表皮生长因子受体酪氨酸激酶抑制剂治疗的 EGFR T790M 突变型非小细胞肺癌患者的疗效:西日本肿瘤学组 8715L 期随机临床试验。
JAMA Oncol. 2021 Mar 1;7(3):386-394. doi: 10.1001/jamaoncol.2020.6758.
5
First-line treatment with irreversible tyrosine kinase inhibitors associated with longer OS in EGFR mutation-positive non-small cell lung cancer.一线使用不可逆的酪氨酸激酶抑制剂与 EGFR 突变阳性非小细胞肺癌的 OS 延长相关。
Thorac Cancer. 2021 Feb;12(3):287-296. doi: 10.1111/1759-7714.13462. Epub 2020 Dec 18.
6
The Combination of Afatinib and Bevacizumab in Untreated EGFR-Mutated Advanced Lung Adenocarcinoma: A Multicenter Observational Study.阿法替尼与贝伐单抗联合用于未经治疗的EGFR突变型晚期肺腺癌:一项多中心观察性研究
Pharmaceuticals (Basel). 2020 Oct 23;13(11):331. doi: 10.3390/ph13110331.
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An Observational Study of Acquired T790M-Dependent Resistance to EGFR-TKI Treatment in Lung Adenocarcinoma Patients in Taiwan.台湾肺腺癌患者中获得性T790M依赖性EGFR-TKI治疗耐药的观察性研究。
Front Oncol. 2020 Sep 4;10:1481. doi: 10.3389/fonc.2020.01481. eCollection 2020.
8
The efficacy of first-line tyrosine kinase inhibitors combined with co-medications in Asian patients with EGFR mutation non-small cell lung cancer.一线酪氨酸激酶抑制剂联合辅助药物治疗亚洲 EGFR 突变型非小细胞肺癌患者的疗效。
Sci Rep. 2020 Sep 11;10(1):14965. doi: 10.1038/s41598-020-71583-w.
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Sequential afatinib and osimertinib in patients with mutation-positive non-small-cell lung cancer: final analysis of the GioTag study.奥希替尼序贯治疗表皮生长因子受体突变阳性非小细胞肺癌患者的研究:GioTag 研究的最终分析。
Future Oncol. 2020 Dec;16(34):2799-2808. doi: 10.2217/fon-2020-0740. Epub 2020 Aug 28.
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Effect of Osimertinib and Bevacizumab on Progression-Free Survival for Patients With Metastatic EGFR-Mutant Lung Cancers: A Phase 1/2 Single-Group Open-Label Trial.奥希替尼联合贝伐珠单抗治疗 EGFR 突变型转移性非小细胞肺癌患者的无进展生存的影响:一项 1/2 期单组开放标签试验
JAMA Oncol. 2020 Jul 1;6(7):1048-1054. doi: 10.1001/jamaoncol.2020.1260.

晚期非小细胞肺癌一线贝伐单抗与表皮生长因子受体酪氨酸激酶抑制剂联合治疗后的T790M检测率(TERRA研究)

T790M detection rate after first-line combination therapy with bevacizumab and EGFR-TKIs in advanced NSCLC (TERRA Study).

作者信息

Kuo Chih-Hsi Scott, Su Po-Lan, Wei Yu-Feng, Ko Jen-Chung, Tseng Jeng-Sen, Su Jian, Chiang Chi-Lu, Chen Chung-Yu, Lin Chien-Chung, Wang Chin-Chou, Ho Chao-Chi, Chang Huang-Chih, Hung Jen-Yu

机构信息

Division of Thoracic Oncology, Department of Thoracic Medicine, Linkou Chang Gung Memorial Hospital Taoyuan 333, Taiwan.

Chang Gung University College of Medicine Taoyuan 333, Taiwan.

出版信息

Am J Cancer Res. 2023 Jul 15;13(7):3100-3112. eCollection 2023.

PMID:37559987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10408489/
Abstract

Real-world data regarding the T790M mutation rate after acquiring resistance to first-line combination therapy with epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) and bevacizumab in patients with advanced non-small-cell lung cancer (NSCLC) are limited. The present study was aimed at analyzing predictors of acquired T790M mutations in this patient group. A total of 107 patients who received first-line combination therapy with EGFR-TKIs and bevacizumab at 11 tertiary referral centers in Taiwan were enrolled in this multicenter retrospective study. Survival data and genomic test results after acquiring resistance were analyzed. We discovered that patients who received a combination of afatinib, a second generation EGFR-TKI, and bevacizumab showed better progression-free survival (PFS). After disease progression, 59 patients (55.1%) were confirmed to test positive for EGFR T790M. A longer duration of first-line therapy could be a predictor of subsequent T790M mutations. To our knowledge, this is one of the few and early studies to demonstrate the T790M mutation rate after first-line combination therapy with an EGFR-TKI and bevacizumab. Whether the longer PFS afforded by the addition of bevacizumab could lead to subsequent T790M mutations needs further investigation.

摘要

关于晚期非小细胞肺癌(NSCLC)患者在对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)和贝伐单抗一线联合治疗产生耐药后T790M突变率的真实世界数据有限。本研究旨在分析该患者群体中获得性T790M突变的预测因素。台湾11家三级转诊中心共有107例接受EGFR-TKIs和贝伐单抗一线联合治疗的患者纳入了这项多中心回顾性研究。分析了产生耐药后的生存数据和基因检测结果。我们发现,接受第二代EGFR-TKI阿法替尼与贝伐单抗联合治疗的患者无进展生存期(PFS)更好。疾病进展后,59例患者(55.1%)被证实EGFR T790M检测呈阳性。一线治疗时间较长可能是后续T790M突变的一个预测因素。据我们所知,这是少数早期研究之一,证明了EGFR-TKI与贝伐单抗一线联合治疗后的T790M突变率。添加贝伐单抗带来的更长PFS是否会导致后续T790M突变需要进一步研究。