egfr突变的非小细胞肺癌的分子检测、治疗模式和结果:双鱼座研究

IF 2.6 4区 医学 Q2 ONCOLOGY
Future oncology Pub Date : 2025-08-01 Epub Date: 2025-07-28 DOI:10.1080/14796694.2025.2529094
Panwen Tian, Lin Wu, Chengzhi Zhou, Jie Tan, Ke Wang, Feng Luo, Yongmei Liu, Yubiao Guo, Yinyin Li, Zhe Liu, Youling Gong, Yongsheng Wang, Jinghong Xian, Weimin Li
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引用次数: 0

摘要

背景:本研究调查了一线(1 L)表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKIs)治疗进展的中国患者的分子检测、治疗模式和预后,强调了临床实践中有限的真实世界数据。方法:在中国16个中心前瞻性纳入连续符合条件的患者。主要终点是二线(2l)治疗模式和临床结果,包括2l治疗的中位无进展生存期(mPFS)和中位总生存期(mOS)。结果:总共有300例患者入组,其中291例患者被纳入完整分析集,213例(73.2%)患者在接受1l治疗后进行了分子检测。30.5%(65/213)有组织标本,66.7%(142/213)有血浆标本。组织标本和血浆标本T790M阳性率分别为53.8%和43.7%。接受第三代(3g) EGFR-TKIs作为2 L治疗的T790M阳性患者的mPFS和mOS分别为14.7个月和32.0个月。T790M阴性患者接受3g EGFR-TKIs、既往EGFR-TKIs加局部治疗和化疗作为2l治疗的mPFS分别为7.6个月、10.2个月和4.9个月。这些患者相应的生存期分别为21.2个月、16.6个月和15.0个月。没有新的安全信号出现。结论:接受3g EGFR-TKIs治疗的第一代(1g)/第二代(2g)获得性EGFR-TKIs耐药患者,尤其是T790M阳性患者,经分子检测后临床预后更好。临床试验注册:该研究已在ClinicalTrials.gov注册(NCT04207775)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular testing, treatment patterns, and outcomes in EGFR-mutated non-small cell lung cancer: the PISCES study.

Background: This study investigated molecular testing, treatment patterns, and prognosis in Chinese patients who progressed from first-line (1 L), epidermal growth factor receptor -tyrosine kinase inhibitors (EGFR-TKIs) therapy, highlighting limited real-world data on clinical practice.

Methods: Consecutive eligible patients were prospectively enrolled in 16-centers in China. The primary endpoints were second-line (2 L) treatment patterns and clinical outcomes, including median progression-free survival (mPFS) and median overall survival (mOS) from 2 L treatment.

Results: Overall, 300 patients were enrolled in the study, and among them, 291 patients were included in the Full Analysis Set, and 213(73.2%) underwent molecular testing, after progression from 1 L therapy. 30.5% (65/213) had tissue samples, while 66.7% (142/213) had plasma samples. In tissue and plasma samples, T790M positive rates were 53.8% and 43.7%, respectively. mPFS and mOS for patients with T790M positive who received third generation (3 G) EGFR-TKIs as 2 L therapy were 14.7 months and 32.0 months, respectively. The mPFS for patients with T790M negative who received 3 G EGFR-TKIs, prior EGFR-TKIs plus local therapy, and chemotherapy as 2 L therapy were 7.6 months, 10.2 months, and 4.9 months, respectively. The corresponding mOS for these patients were 21.2 months, 16.6 months, and 15.0 months, respectively. No new safety signal emerged.

Conclusions: Patients with acquired resistance to first generation (1 G)/second generation (2 G) EGFR-TKIs receiving 3 G EGFR-TKIs, especially T790M positive, showed better clinical outcomes after molecular testing.

Clinical trial registration: The study has been registered at ClinicalTrials.gov (NCT04207775).

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来源期刊
Future oncology
Future oncology ONCOLOGY-
CiteScore
5.40
自引率
3.00%
发文量
335
审稿时长
4-8 weeks
期刊介绍: Future Oncology (ISSN 1479-6694) provides a forum for a new era of cancer care. The journal focuses on the most important advances and highlights their relevance in the clinical setting. Furthermore, Future Oncology delivers essential information in concise, at-a-glance article formats - vital in delivering information to an increasingly time-constrained community. The journal takes a forward-looking stance toward the scientific and clinical issues, together with the economic and policy issues that confront us in this new era of cancer care. The journal includes literature awareness such as the latest developments in radiotherapy and immunotherapy, concise commentary and analysis, and full review articles all of which provide key findings, translational to the clinical setting.
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