通过数字液滴聚合酶链反应 ddPCR 和新一代测序技术检测第三代表皮生长因子受体酪氨酸激酶抑制剂对不同 T790M 状态的晚期 NSCLC 的疗效。

IF 2.9 3区 医学 Q2 ONCOLOGY
Expert Review of Anticancer Therapy Pub Date : 2024-03-01 Epub Date: 2024-04-17 DOI:10.1080/14737140.2024.2334807
Ziyi Xu, Yan Li, Lin Wang, Xuezhi Hao, Jianming Ying, Junling Li, Puyuan Xing
{"title":"通过数字液滴聚合酶链反应 ddPCR 和新一代测序技术检测第三代表皮生长因子受体酪氨酸激酶抑制剂对不同 T790M 状态的晚期 NSCLC 的疗效。","authors":"Ziyi Xu, Yan Li, Lin Wang, Xuezhi Hao, Jianming Ying, Junling Li, Puyuan Xing","doi":"10.1080/14737140.2024.2334807","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>We hypothesize that digital droplet polymerase chain reaction (ddPCR) would optimize the treatment strategies in epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) relapsed patients. In this study, we compared the efficacy of third-generation TKIs with various T790M statuses via ddPCR and next-generation sequencing (NGS).</p><p><strong>Methods: </strong>NGS was performed on blood samples of patients progressed from previous EGFR-TKIs for resistance mechanism. T790M-negative patients received further liquid biopsy using ddPCR for T790M detection.</p><p><strong>Results: </strong>A cohort of 40 patients were enrolled, with 30.0% (12/40) T790M-positive via NGS (Group A). In another 28 T790M-negative patients by NGS, 11 (39.3%) were T790M-positive (Group B) and 17 (60.7%) were T790M-negative (Group C) via ddPCR. A relatively longer progression-free survival (PFS) was observed in group A (NR) and group B (10.0 months, 95% CI 7.040-12.889) than in group C (7.0 months, 95% CI 0.000-15.219), with no significant difference across all three groups (<i>p</i> = 0.196), or between group B and C (<i>p</i> = 0.412). EGFR-sensitive mutation correlated with inferior PFS (<i>p</i> = 0.041) and ORR (<i>p</i> = 0.326), and a significantly lower DCR (<i>p</i> = 0.033) in T790M-negative patients via NGS (<i>n</i> = 28).</p><p><strong>Conclusion: </strong>This study indicates that ddPCR may contribute as a supplement to NGS in liquid biopsies for T790M detection in EGFR-TKIs relapsed patients and help to optimize the treatment strategies, especially for those without coexistence of EGFR-sensitive mutation.</p><p><strong>Trial registration: </strong>www.clinicaltrials.gov identifier is NCT05458726.</p>","PeriodicalId":12099,"journal":{"name":"Expert Review of Anticancer Therapy","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy of third-generation epidermal growth factor receptor-tyrosine kinase inhibitors in advanced NSCLC with different T790M statuses tested via digital droplet polymerase chain reaction ddPCR and next-generation sequencing.\",\"authors\":\"Ziyi Xu, Yan Li, Lin Wang, Xuezhi Hao, Jianming Ying, Junling Li, Puyuan Xing\",\"doi\":\"10.1080/14737140.2024.2334807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>We hypothesize that digital droplet polymerase chain reaction (ddPCR) would optimize the treatment strategies in epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) relapsed patients. In this study, we compared the efficacy of third-generation TKIs with various T790M statuses via ddPCR and next-generation sequencing (NGS).</p><p><strong>Methods: </strong>NGS was performed on blood samples of patients progressed from previous EGFR-TKIs for resistance mechanism. T790M-negative patients received further liquid biopsy using ddPCR for T790M detection.</p><p><strong>Results: </strong>A cohort of 40 patients were enrolled, with 30.0% (12/40) T790M-positive via NGS (Group A). In another 28 T790M-negative patients by NGS, 11 (39.3%) were T790M-positive (Group B) and 17 (60.7%) were T790M-negative (Group C) via ddPCR. A relatively longer progression-free survival (PFS) was observed in group A (NR) and group B (10.0 months, 95% CI 7.040-12.889) than in group C (7.0 months, 95% CI 0.000-15.219), with no significant difference across all three groups (<i>p</i> = 0.196), or between group B and C (<i>p</i> = 0.412). EGFR-sensitive mutation correlated with inferior PFS (<i>p</i> = 0.041) and ORR (<i>p</i> = 0.326), and a significantly lower DCR (<i>p</i> = 0.033) in T790M-negative patients via NGS (<i>n</i> = 28).</p><p><strong>Conclusion: </strong>This study indicates that ddPCR may contribute as a supplement to NGS in liquid biopsies for T790M detection in EGFR-TKIs relapsed patients and help to optimize the treatment strategies, especially for those without coexistence of EGFR-sensitive mutation.</p><p><strong>Trial registration: </strong>www.clinicaltrials.gov identifier is NCT05458726.</p>\",\"PeriodicalId\":12099,\"journal\":{\"name\":\"Expert Review of Anticancer Therapy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2024-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Expert Review of Anticancer Therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/14737140.2024.2334807\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/4/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Review of Anticancer Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/14737140.2024.2334807","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/4/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的:我们假设数字液滴聚合酶链反应(ddPCR)将优化表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKI)的治疗策略:我们假设数字液滴聚合酶链反应(ddPCR)将优化表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKIs)复发患者的治疗策略。在本研究中,我们通过 ddPCR 和新一代测序(NGS)比较了不同 T790M 状态的第三代 TKIs 的疗效:对既往使用过 EGFR-TKIs 的进展期患者的血液样本进行 NGS 检测,以了解耐药机制。T790M阴性患者进一步接受液体活检,使用ddPCR检测T790M:结果:40 例患者中,30.0%(12/40)通过 NGS 检测出 T790M 阳性(A 组)。在另外 28 例 NGS T790M 阴性患者中,11 例(39.3%)为 T790M 阳性(B 组),17 例(60.7%)为 ddPCR T790M 阴性(C 组)。与 C 组(7.0 个月,95%CI 0.000-15.219)相比,A 组(NR)和 B 组(10.0 个月,95%CI 7.040-12.889)的无进展生存期(PFS)相对较长,三组之间(P = 0.196)或 B 组与 C 组之间(P = 0.412)无显著差异。表皮生长因子受体敏感突变与较差的PFS(p = 0.041)和ORR(p = 0.326)相关,通过NGS检测的T790M阴性患者(n = 28)的DCR显著较低(p = 0.033):本研究表明,ddPCR可作为NGS的补充,用于EGFR-TKIs复发患者液体活检中T790M的检测,并有助于优化治疗策略,尤其是对于那些不同时存在EGFR敏感突变的患者。试验注册:www.clinicaltrials.gov identifier is NCT05458726。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of third-generation epidermal growth factor receptor-tyrosine kinase inhibitors in advanced NSCLC with different T790M statuses tested via digital droplet polymerase chain reaction ddPCR and next-generation sequencing.

Objectives: We hypothesize that digital droplet polymerase chain reaction (ddPCR) would optimize the treatment strategies in epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) relapsed patients. In this study, we compared the efficacy of third-generation TKIs with various T790M statuses via ddPCR and next-generation sequencing (NGS).

Methods: NGS was performed on blood samples of patients progressed from previous EGFR-TKIs for resistance mechanism. T790M-negative patients received further liquid biopsy using ddPCR for T790M detection.

Results: A cohort of 40 patients were enrolled, with 30.0% (12/40) T790M-positive via NGS (Group A). In another 28 T790M-negative patients by NGS, 11 (39.3%) were T790M-positive (Group B) and 17 (60.7%) were T790M-negative (Group C) via ddPCR. A relatively longer progression-free survival (PFS) was observed in group A (NR) and group B (10.0 months, 95% CI 7.040-12.889) than in group C (7.0 months, 95% CI 0.000-15.219), with no significant difference across all three groups (p = 0.196), or between group B and C (p = 0.412). EGFR-sensitive mutation correlated with inferior PFS (p = 0.041) and ORR (p = 0.326), and a significantly lower DCR (p = 0.033) in T790M-negative patients via NGS (n = 28).

Conclusion: This study indicates that ddPCR may contribute as a supplement to NGS in liquid biopsies for T790M detection in EGFR-TKIs relapsed patients and help to optimize the treatment strategies, especially for those without coexistence of EGFR-sensitive mutation.

Trial registration: www.clinicaltrials.gov identifier is NCT05458726.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.10
自引率
3.00%
发文量
100
审稿时长
4-8 weeks
期刊介绍: Expert Review of Anticancer Therapy (ISSN 1473-7140) provides expert appraisal and commentary on the major trends in cancer care and highlights the performance of new therapeutic and diagnostic approaches. Coverage includes tumor management, novel medicines, anticancer agents and chemotherapy, biological therapy, cancer vaccines, therapeutic indications, biomarkers and diagnostics, and treatment guidelines. All articles are subject to rigorous peer-review, and the journal makes an essential contribution to decision-making in cancer care. Comprehensive coverage in each review is complemented by the unique Expert Review format and includes the following sections: Expert Opinion - a personal view of the data presented in the article, a discussion on the developments that are likely to be important in the future, and the avenues of research likely to become exciting as further studies yield more detailed results Article Highlights – an executive summary of the author’s most critical points.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信