Clinical Sequence Revealed the Prevalence and Biological Significance of Somatic Pathogenic Variants in Thoracic Cancer: Implications for Germline Status.

IF 3.3 3区 医学 Q2 ONCOLOGY
Takahiro Fukushima, Kohei Nakamura, Hideki Terai, Keiko Ohgino, Ryutaro Kawano, Marin Ishikawa, Katsura Emoto, Hatsuyo Takaoka, Ayaka Saito, Fumimaro Ito, Shigenari Nukaga, Shinnosuke Ikemura, Ichiro Kawada, Kenta Masuda, Hiroyuki Yasuda, Hajime Okita, Keisuke Asakura, Kenzo Soejima, Kenjiro Kosaki, Hiroshi Nishihara, Koichi Fukunaga
{"title":"Clinical Sequence Revealed the Prevalence and Biological Significance of Somatic Pathogenic Variants in Thoracic Cancer: Implications for Germline Status.","authors":"Takahiro Fukushima, Kohei Nakamura, Hideki Terai, Keiko Ohgino, Ryutaro Kawano, Marin Ishikawa, Katsura Emoto, Hatsuyo Takaoka, Ayaka Saito, Fumimaro Ito, Shigenari Nukaga, Shinnosuke Ikemura, Ichiro Kawada, Kenta Masuda, Hiroyuki Yasuda, Hajime Okita, Keisuke Asakura, Kenzo Soejima, Kenjiro Kosaki, Hiroshi Nishihara, Koichi Fukunaga","doi":"10.1016/j.cllc.2025.03.012","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Presumed germline pathogenic variants (PGPVs) are occasionally detected in thoracic cancer and their frequency and functional significance remain underexplored. We investigated the prevalence and biological significance of PGPVs identified in comprehensive genomic profiling (CGP) panels in patients with thoracic cancer.</p><p><strong>Patients and methods: </strong>Between January 2021 and August 2023, 204 patients with thoracic cancer were included in this study. A somatic cancer genomic profile system-FoundationOne CDx or an in-house system (Rapid-Neo)-was used for next-generation sequencing-based cancer gene panel tests. Potential PGPVs were identified by evaluating the variant allele frequency (VAF; cutoff > 10%) and pathogenicity based on ClinVar.</p><p><strong>Results: </strong>PGPVs were detected at a frequency of 9.7% from cohort 1 and 8.1% from cohort 2 in thoracic cancer, based on real-world comprehensive genomic profiling panel testing. Copy number plot did not indicate any homologous recombination deficiency patterns in cases with BRCA1, BRCA2, and RAD51D pathogenic variants in thoracic cancer compared with those in hereditary breast and ovarian cancers. Only one hit of MSH6 pathogenic germline variant was observed for lung cancer tissue in the case of Lynch syndrome; therefore, high tumor mutational burden/microsatellite instability or mismatch repair deficiency was not observed, unlike that in endometrial cancer tissue in the same individual.</p><p><strong>Conclusion: </strong>This study underscores the importance of identifying PGPVs through CGP testing conducted in patients with thoracic cancer. Using frequency and functional analysis. Further investigation is warranted regarding the clinical significance of these PGPVs in managing patients with thoracic cancer and their families.</p>","PeriodicalId":10490,"journal":{"name":"Clinical lung cancer","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical lung cancer","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.cllc.2025.03.012","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: Presumed germline pathogenic variants (PGPVs) are occasionally detected in thoracic cancer and their frequency and functional significance remain underexplored. We investigated the prevalence and biological significance of PGPVs identified in comprehensive genomic profiling (CGP) panels in patients with thoracic cancer.

Patients and methods: Between January 2021 and August 2023, 204 patients with thoracic cancer were included in this study. A somatic cancer genomic profile system-FoundationOne CDx or an in-house system (Rapid-Neo)-was used for next-generation sequencing-based cancer gene panel tests. Potential PGPVs were identified by evaluating the variant allele frequency (VAF; cutoff > 10%) and pathogenicity based on ClinVar.

Results: PGPVs were detected at a frequency of 9.7% from cohort 1 and 8.1% from cohort 2 in thoracic cancer, based on real-world comprehensive genomic profiling panel testing. Copy number plot did not indicate any homologous recombination deficiency patterns in cases with BRCA1, BRCA2, and RAD51D pathogenic variants in thoracic cancer compared with those in hereditary breast and ovarian cancers. Only one hit of MSH6 pathogenic germline variant was observed for lung cancer tissue in the case of Lynch syndrome; therefore, high tumor mutational burden/microsatellite instability or mismatch repair deficiency was not observed, unlike that in endometrial cancer tissue in the same individual.

Conclusion: This study underscores the importance of identifying PGPVs through CGP testing conducted in patients with thoracic cancer. Using frequency and functional analysis. Further investigation is warranted regarding the clinical significance of these PGPVs in managing patients with thoracic cancer and their families.

临床序列揭示了胸癌中躯体致病变异的患病率和生物学意义:对种系状态的影响。
目的:推定的种系致病变异(PGPVs)偶尔在胸部癌中被检测到,其频率和功能意义仍未得到充分研究。我们研究了综合基因组图谱(CGP)在胸部癌患者中鉴定的PGPVs的患病率和生物学意义。患者和方法:2021年1月至2023年8月期间,204例胸部癌症患者纳入本研究。体细胞癌症基因组图谱系统foundationone CDx或内部系统Rapid-Neo被用于下一代基于测序的癌症基因面板测试。通过评估变异等位基因频率(VAF;阻断率为10%)和致病性基于ClinVar。结果:基于真实世界的全面基因组谱面板测试,PGPVs在队列1和队列2中检测到的频率分别为9.7%和8.1%。与遗传性乳腺癌和卵巢癌相比,拷贝数图未显示乳腺癌中BRCA1、BRCA2和RAD51D致病性变异的任何同源重组缺陷模式。在Lynch综合征的肺癌组织中只观察到1个MSH6致病种系变异;因此,与同一个体的子宫内膜癌组织不同,未观察到高肿瘤突变负担/微卫星不稳定性或错配修复缺陷。结论:本研究强调了通过胸廓癌患者的CGP检测识别PGPVs的重要性。使用频率和功能分析。这些PGPVs在胸癌患者及其家属管理中的临床意义有待进一步研究。
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
Clinical lung cancer
Clinical lung cancer 医学-肿瘤学
CiteScore
7.00
自引率
2.80%
发文量
159
审稿时长
24 days
期刊介绍: Clinical Lung Cancer is a peer-reviewed bimonthly journal that publishes original articles describing various aspects of clinical and translational research of lung cancer. Clinical Lung Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of lung cancer. The main emphasis is on recent scientific developments in all areas related to lung cancer. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
×
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