Abstract 454: The landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations

Ningbo Liu, Fuyu Gong
{"title":"Abstract 454: The landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations","authors":"Ningbo Liu, Fuyu Gong","doi":"10.1158/1538-7445.AM2021-454","DOIUrl":null,"url":null,"abstract":"Background: Results from previous studies indicated that lung cancer patients harboring EGFR sensitizing mutations may receive unfavorable outcomes from immunotherapy. The present study aims to investigate the landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations. Methods: Tissue samples were subjected to NGS in a College of American Pathologists-certified and Clinical Laboratory Improvement Amendments-accredited lab for driver oncogene mutations and PD-L1 expression. Results: A total of 22143 lung cancer patients were selected, there are 2120 patients have the driver oncogene mutation, including 1115 (5.04%) ALK positive cases,498 (2.25%) MET positive cases,239(1.08%) RET positive cases,182(0.82%) BRAF positive cases, 72 (0.33%) ROS1 positive cases and 14 (0.03%) NTRK positive cases. Among all the driver oncogene mutation patients, 481 patients have been collected tumor tissue, and the PD-L1 expression have been tested by FDA-approved 22C3 antibodies. Among all the driver oncogene mutation cases assessed PD-L1 expression (n=481), low PD-L1 expression levels ( Conclusion: Our study supported that NSCLC patients harboring sensitizing oncogenic mutations may potentially benefit from anti-PD-1/L1 especially for those with positive indicators of immunotherapy with strong positive PD-L1 expression. Citation Format: Ningbo Liu, Fuyu Gong. The landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 454.","PeriodicalId":10518,"journal":{"name":"Clinical Research (Excluding Clinical Trials)","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Research (Excluding Clinical Trials)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/1538-7445.AM2021-454","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Results from previous studies indicated that lung cancer patients harboring EGFR sensitizing mutations may receive unfavorable outcomes from immunotherapy. The present study aims to investigate the landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations. Methods: Tissue samples were subjected to NGS in a College of American Pathologists-certified and Clinical Laboratory Improvement Amendments-accredited lab for driver oncogene mutations and PD-L1 expression. Results: A total of 22143 lung cancer patients were selected, there are 2120 patients have the driver oncogene mutation, including 1115 (5.04%) ALK positive cases,498 (2.25%) MET positive cases,239(1.08%) RET positive cases,182(0.82%) BRAF positive cases, 72 (0.33%) ROS1 positive cases and 14 (0.03%) NTRK positive cases. Among all the driver oncogene mutation patients, 481 patients have been collected tumor tissue, and the PD-L1 expression have been tested by FDA-approved 22C3 antibodies. Among all the driver oncogene mutation cases assessed PD-L1 expression (n=481), low PD-L1 expression levels ( Conclusion: Our study supported that NSCLC patients harboring sensitizing oncogenic mutations may potentially benefit from anti-PD-1/L1 especially for those with positive indicators of immunotherapy with strong positive PD-L1 expression. Citation Format: Ningbo Liu, Fuyu Gong. The landscape of PD-L1 expression in lung cancer harboring driver oncogene mutations except EGFR mutations [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 454.
摘要:PD-L1在除EGFR突变外具有驱动癌基因突变的肺癌中的表达格局
背景:先前的研究结果表明,携带EGFR致敏突变的肺癌患者可能会接受免疫治疗的不良结果。本研究旨在探讨除EGFR突变外的驱动癌基因突变的肺癌中PD-L1的表达情况。方法:组织样本在美国病理学家学院认证和临床实验室改进修正案认可的实验室进行NGS检测驱动癌基因突变和PD-L1表达。结果:共入选肺癌患者22143例,其中驱动癌基因突变2120例,其中ALK阳性1115例(5.04%),MET阳性498例(2.25%),RET阳性239例(1.08%),BRAF阳性182例(0.82%),ROS1阳性72例(0.33%),NTRK阳性14例(0.03%)。在所有驱动癌基因突变患者中,收集了481例患者的肿瘤组织,并使用fda批准的22C3抗体检测PD-L1表达。在所有评估PD-L1表达的驱动癌基因突变病例中(n=481), PD-L1表达水平低(结论:本研究支持具有致敏性癌基因突变的非小细胞肺癌患者可能潜在地受益于抗pd -1/L1,特别是那些免疫治疗指标阳性且PD-L1表达强烈的患者。引用格式:刘宁波,龚福玉。肺癌中除EGFR外驱动癌基因突变的PD-L1表达格局[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):454。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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