• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于下一代测序评估中国 EGFR 阳性晚期 NSCLC 患者的共突变预后:一项回顾性研究。

Evaluate the Prognosis of Comutation in Chinese Patients with EGFR-Positive Advanced NSCLC Using Next-Generation Sequencing: A Retrospective Study.

机构信息

Medical College, 38043Yangzhou University, Yangzhou, Jiangsu, China.

Institute of Oncology, 370089Northern Jiangsu People's Hospital, Yangzhou, Jiangsu, China.

出版信息

Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221138213. doi: 10.1177/15330338221138213.

DOI:10.1177/15330338221138213
PMID:36524293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9761218/
Abstract

The purpose of this study was to investigate the effect of and comutations on the clinical efficacy of EGFR tyrosine kinase inhibitors (TKIs) in Chinese patients with advanced EGFR-positive nonsmall-cell lung cancer (NSCLC). Tissue samples and information from 65 patients with advanced NSCLC in Northern Jiangsu People's Hospital were collected and analyzed by next-generation sequencing (NGS). Progression-free survival (PFS) and total survival (OS) were the main endpoints, and the objective response rate (ORR) and disease control rate (DCR) were the secondary endpoints. : Among 65 patients, 17 had and wild-type mutations (), 36 had mutant and wild-type mutations (), and 12 had coexisting mutations (). When 12 patients with comutation were compared with the other two groups (, ), mPFS and mOS are significantly lower than those in the other two groups (mPFS: 4.1 months vs 6.0 months, 12.3 months, HR: 0.769, 95% CI: 4.592-7.608,   =  .047. mOS: 14.6 months vs 24.1 months, 31.5 months, HR: 3.170, 95% CI: 18.786-31.214, < .001), and the ORR, DCR of patients with comutation was lower than that of the other two groups (ORR, 25% vs 44.4%, 70.6%,   =  .045. DCR, 58.3% vs 72.2%, 82.4%,   =  .365). Patients with comutations with EGFR-positive advanced NSCLC are more likely to develop drug resistance after early treatment with EGFR-TKIs and have a worse clinical outcome.

摘要

本研究旨在探讨 及 共突变对中国晚期 EGFR 阳性非小细胞肺癌(NSCLC)患者接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)治疗临床疗效的影响。通过下一代测序(NGS),收集并分析了来自苏北人民医院的 65 例晚期 NSCLC 患者的组织样本和信息。无进展生存期(PFS)和总生存期(OS)是主要终点,客观缓解率(ORR)和疾病控制率(DCR)是次要终点。结果:在 65 例患者中,17 例存在 和 野生型突变(),36 例存在 突变和 野生型突变(),12 例存在 共突变()。与另外两组(,)相比,当比较 12 例 共突变患者时,mPFS 和 mOS 明显低于另外两组(mPFS:4.1 个月比 6.0 个月和 12.3 个月,HR:0.769,95%CI:4.592-7.608,=0.047。mOS:14.6 个月比 24.1 个月和 31.5 个月,HR:3.170,95%CI:18.786-31.214,<0.001),且 共突变患者的 ORR 和 DCR 均低于另外两组(ORR,25%比 44.4%和 70.6%,=0.045。DCR,58.3%比 72.2%和 82.4%,=0.365)。患有 及 共突变的 EGFR 阳性晚期 NSCLC 患者在接受 EGFR-TKIs 早期治疗后更容易发生耐药,临床结局更差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/71a0abdc4d73/10.1177_15330338221138213-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/2b8259ac614f/10.1177_15330338221138213-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/8551e8f7b683/10.1177_15330338221138213-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/c4213cfd992b/10.1177_15330338221138213-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/71a0abdc4d73/10.1177_15330338221138213-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/2b8259ac614f/10.1177_15330338221138213-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/8551e8f7b683/10.1177_15330338221138213-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/c4213cfd992b/10.1177_15330338221138213-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af4b/9761218/71a0abdc4d73/10.1177_15330338221138213-fig4.jpg

相似文献

1
Evaluate the Prognosis of Comutation in Chinese Patients with EGFR-Positive Advanced NSCLC Using Next-Generation Sequencing: A Retrospective Study.基于下一代测序评估中国 EGFR 阳性晚期 NSCLC 患者的共突变预后:一项回顾性研究。
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221138213. doi: 10.1177/15330338221138213.
2
A high number of co-occurring genomic alterations detected by NGS is associated with worse clinical outcomes in advanced EGFR-mutant lung adenocarcinoma: Data from LATAM population.通过二代测序(NGS)检测到的大量同时出现的基因组改变与晚期表皮生长因子受体(EGFR)突变型肺腺癌的更差临床结局相关:来自拉丁美洲人群的数据。
Lung Cancer. 2022 Dec;174:133-140. doi: 10.1016/j.lungcan.2022.11.002. Epub 2022 Nov 9.
3
Prognostic value of TP53 concurrent mutations for EGFR- TKIs and ALK-TKIs based targeted therapy in advanced non-small cell lung cancer: a meta-analysis.TP53 并发突变对晚期非小细胞肺癌 EGFR-TKIs 和 ALK-TKIs 靶向治疗的预后价值:一项荟萃分析。
BMC Cancer. 2020 Apr 16;20(1):328. doi: 10.1186/s12885-020-06805-5.
4
Efficacy and safety analyses of epidermal growth factor receptor tyrosine kinase inhibitors combined with chemotherapy in the treatment of advanced non-small-cell lung cancer with an EGFR/TP53 co-mutation.表皮生长因子受体酪氨酸激酶抑制剂联合化疗治疗 EGFR/TP53 共突变的晚期非小细胞肺癌的疗效和安全性分析。
BMC Cancer. 2022 Dec 12;22(1):1295. doi: 10.1186/s12885-022-10391-z.
5
Next-generation sequencing of tissue and circulating tumor DNA: Resistance mechanisms to EGFR targeted therapy in a cohort of patients with advanced non-small cell lung cancer.组织和循环肿瘤 DNA 的下一代测序:在一组晚期非小细胞肺癌患者中对 EGFR 靶向治疗的耐药机制。
Cancer Med. 2021 Jul;10(14):4697-4709. doi: 10.1002/cam4.3948. Epub 2021 Jun 25.
6
Pooled Analysis of the Prognostic and Predictive Effects of TP53 Comutation Status Combined With KRAS or EGFR Mutation in Early-Stage Resected Non-Small-Cell Lung Cancer in Four Trials of Adjuvant Chemotherapy.在四项辅助化疗试验中,对早期切除的非小细胞肺癌中TP53突变状态联合KRAS或EGFR突变的预后和预测作用的汇总分析。
J Clin Oncol. 2017 Jun 20;35(18):2018-2027. doi: 10.1200/JCO.2016.71.2893. Epub 2017 Apr 28.
7
Concurrent Genetic Alterations Predict the Progression to Target Therapy in EGFR-Mutated Advanced NSCLC.同时存在的基因改变可预测 EGFR 突变型晚期 NSCLC 进展为靶向治疗。
J Thorac Oncol. 2019 Feb;14(2):193-202. doi: 10.1016/j.jtho.2018.10.150. Epub 2018 Nov 1.
8
Prognostic and predictive effects of TP53 co-mutation in patients with EGFR-mutated non-small cell lung cancer (NSCLC).TP53共突变对表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者的预后和预测作用。
Lung Cancer. 2017 Sep;111:23-29. doi: 10.1016/j.lungcan.2017.06.014. Epub 2017 Jun 24.
9
Association of Tumor Protein p53 and Ataxia-Telangiectasia Mutated Comutation With Response to Immune Checkpoint Inhibitors and Mortality in Patients With Non-Small Cell Lung Cancer.肿瘤蛋白 p53 和共济失调毛细血管扩张突变与非小细胞肺癌患者免疫检查点抑制剂反应和死亡率的关联。
JAMA Netw Open. 2019 Sep 4;2(9):e1911895. doi: 10.1001/jamanetworkopen.2019.11895.
10
Concurrent TP53 mutations predict poor outcomes of EGFR-TKI treatments in Chinese patients with advanced NSCLC.同时存在的TP53突变预示着中国晚期非小细胞肺癌患者接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗的预后较差。
Cancer Manag Res. 2019 Jun 21;11:5665-5675. doi: 10.2147/CMAR.S201513. eCollection 2019.

引用本文的文献

1
Effects of Tp53 Gene Mutations on the Survival of Non-Small Cell Lung Cancer (NSCLC); A Short Review.Tp53基因突变对非小细胞肺癌(NSCLC)生存的影响;简短综述。
Cancer Manag Res. 2025 Jan 15;17:65-82. doi: 10.2147/CMAR.S495006. eCollection 2025.
2
The regulation roles of miRNAs in Helicobacter pylori infection.miRNAs 在幽门螺杆菌感染中的调控作用。
Clin Transl Oncol. 2023 Jul;25(7):1929-1939. doi: 10.1007/s12094-023-03094-9. Epub 2023 Feb 13.

本文引用的文献

1
Evaluation of Pembrolizumab Monotherapy Efficacy in Advanced Non-Small-Cell Lung Cancer by Serial Monitoring of Circulating Tumor DNA Using Next-Generation Sequencing.通过下一代测序对循环肿瘤DNA进行连续监测评估帕博利珠单抗单药治疗晚期非小细胞肺癌的疗效
Clin Med Insights Oncol. 2022 Feb 17;16:11795549221075326. doi: 10.1177/11795549221075326. eCollection 2022.
2
OncoDB: an interactive online database for analysis of gene expression and viral infection in cancer.OncoDB:一个交互式在线数据库,用于分析癌症中的基因表达和病毒感染。
Nucleic Acids Res. 2022 Jan 7;50(D1):D1334-D1339. doi: 10.1093/nar/gkab970.
3
Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report.
晚期肺癌患者中非小细胞肺癌向小细胞肺癌转化:1 例病例报告。
J Int Med Res. 2021 Aug;49(8):3000605211035005. doi: 10.1177/03000605211035005.
4
Targeting c-Myc to Overcome Acquired Resistance of EGFR Mutant NSCLC Cells to the Third-Generation EGFR Tyrosine Kinase Inhibitor, Osimertinib.针对 c-Myc 克服第三代 EGFR 酪氨酸激酶抑制剂奥希替尼治疗 EGFR 突变型 NSCLC 获得性耐药。
Cancer Res. 2021 Sep 15;81(18):4822-4834. doi: 10.1158/0008-5472.CAN-21-0556. Epub 2021 Jul 21.
5
Dynamic cfDNA Analysis by NGS in T790M-Positive Advanced NSCLC Patients Failed to the First-Generation EGFR-TKIs.对第一代表皮生长因子受体酪氨酸激酶抑制剂治疗失败的T790M阳性晚期非小细胞肺癌患者进行二代测序动态循环游离DNA分析
Front Oncol. 2021 Mar 25;11:643199. doi: 10.3389/fonc.2021.643199. eCollection 2021.
6
Prototypical oncogene family Myc defines unappreciated distinct lineage states of small cell lung cancer.典型癌基因家族Myc定义了小细胞肺癌未被认识的不同谱系状态。
Sci Adv. 2021 Jan 29;7(5). doi: 10.1126/sciadv.abc2578. Print 2021 Jan.
7
C-MYC-induced upregulation of LINC01503 promotes progression of non-small cell lung cancer.C-MYC 诱导的 LINC01503 上调促进非小细胞肺癌的进展。
Eur Rev Med Pharmacol Sci. 2020 Nov;24(21):11120-11127. doi: 10.26355/eurrev_202011_23599.
8
Digital PCR for the Analysis of Copy Number Variation in Lung Cancer.数字 PCR 分析肺癌中的拷贝数变异。
Dis Markers. 2020 Sep 19;2020:4176376. doi: 10.1155/2020/4176376. eCollection 2020.
9
Myc linked to dysregulation of cholesterol transport and storage in nonsmall cell lung cancer.Myc 与非小细胞肺癌中胆固醇转运和储存的失调有关。
J Lipid Res. 2020 Nov;61(11):1390-1399. doi: 10.1194/jlr.RA120000899. Epub 2020 Aug 4.
10
lncRNAs as Potential Targets in Small Cell Lung Cancer: MYC -dependent Regulation.lncRNAs 作为小细胞肺癌的潜在靶点:MYC 依赖性调控。
Anticancer Agents Med Chem. 2020;20(17):2074-2081. doi: 10.2174/1871520620666200721130700.