Suppr超能文献

用于非小细胞肺癌综合分子检测的EBUS-TBNA细胞学样本

EBUS-TBNA Cytological Samples for Comprehensive Molecular Testing in Non-Small Cell Lung Cancer.

作者信息

Martin-Deleon Roberto, Teixido Cristina, Lucena Carmen Mª, Martinez Daniel, Fontana Ainhoa, Reyes Roxana, García Mireia, Viñolas Nuria, Vollmer Ivan, Sanchez Marcelo, Jares Pedro, Pérez Francisco Manuel, Vega Naiara, Marin Elba, Marrades Ramón Mª, Agustí Carlos, Reguart Noemi

机构信息

Department of Respiratory Medicine, Thoracic Oncology Unit, Hospital Clínic of Barcelona, 08036 Barcelona, Spain.

Translational Genomic and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), 08036 Barcelona, Spain.

出版信息

Cancers (Basel). 2021 Apr 25;13(9):2084. doi: 10.3390/cancers13092084.

Abstract

Clinical guidelines promote the identification of several targetable biomarkers to drive treatment decisions in advanced non-small cell lung cancer (NSCLC), but half of all patients do not have a viable biopsy. Specimens from endobronchial-ultrasound transbronchial needle aspiration (EBUS-TBNA) are an alternative source of material for the initial diagnosis of NSCLC, however their usefulness for a complete molecular characterization remains controversial. EBUS-TBNA samples were prospectively tested for several biomarkers by next-generation sequencing (NGS), nCounter, and immunohistochemistry (PD-L1). The primary objectives were to assess the sensitivity of EBUS-TBNA samples for a comprehensive molecular characterization and to compare its performance to the reference standard of biopsy samples. Seventy-two EBUS-TBNA procedures were performed, and 42 NSCLC patients were diagnosed. Among all cytological samples, 92.9% were successfully genotyped by NGS, 95.2% by nCounter, and 100% by immunohistochemistry. There were 29 paired biopsy samples; 79.3% samples had enough tumor material for genomic genotyping, and 96.6% for PD-L1 immunohistochemistry. A good concordance was found between both sources of material: 88.9% for PD-L1, 100% for NGS and nCounter. EBUS-TBNA is a feasible alternative source of material for NSCLC genotyping and allows the identification of patient candidates for personalized therapies with high concordance when compared with biopsy.

摘要

临床指南提倡识别多种可靶向生物标志物,以指导晚期非小细胞肺癌(NSCLC)的治疗决策,但所有患者中有一半没有可行的活检样本。经支气管超声引导下经支气管针吸活检(EBUS-TBNA)的样本是NSCLC初始诊断的另一种材料来源,然而其对完整分子特征分析的有用性仍存在争议。通过新一代测序(NGS)、nCounter和免疫组织化学(PD-L1)对EBUS-TBNA样本进行了前瞻性的几种生物标志物检测。主要目的是评估EBUS-TBNA样本进行全面分子特征分析的敏感性,并将其性能与活检样本的参考标准进行比较。共进行了72例EBUS-TBNA操作,诊断出42例NSCLC患者。在所有细胞学样本中,NGS成功基因分型的比例为92.9%,nCounter为95.2%,免疫组织化学为100%。有29对活检样本;79.3%的样本有足够的肿瘤材料用于基因组基因分型,96.6%的样本可用于PD-L1免疫组织化学检测。两种材料来源之间发现了良好的一致性:PD-L1为88.9%,NGS和nCounter为100%。EBUS-TBNA是NSCLC基因分型的一种可行的替代材料来源,与活检相比,它能够高度一致地识别适合个性化治疗的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c713/8123471/245b825373f6/cancers-13-02084-g001.jpg

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