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Overall Survival with Osimertinib in Resected -Mutated NSCLC.奥希替尼治疗可切除突变型 NSCLC 的总生存期。
N Engl J Med. 2023 Jul 13;389(2):137-147. doi: 10.1056/NEJMoa2304594. Epub 2023 Jun 4.
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Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine.精准医疗时代非小细胞肺癌临床医生及患者指南。
Front Oncol. 2023 Feb 1;13:1124167. doi: 10.3389/fonc.2023.1124167. eCollection 2023.
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Updates in pathology and molecular diagnostics to inform the evolving landscape of thoracic surgery and oncology.病理学与分子诊断学的进展,为胸外科手术与肿瘤学不断变化的领域提供信息。
J Surg Oncol. 2023 Feb;127(2):244-257. doi: 10.1002/jso.27184.
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Deep-Learning Algorithm and Concomitant Biomarker Identification for NSCLC Prediction Using Multi-Omics Data Integration.基于多组学数据整合的深度学习算法及伴随生物标志物识别用于 NSCLC 预测。
Biomolecules. 2022 Dec 8;12(12):1839. doi: 10.3390/biom12121839.
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Cerebrospinal fluid circulating tumor DNA depicts profiling of brain metastasis in NSCLC.脑脊液循环肿瘤 DNA 描绘了 NSCLC 脑转移的图谱。
Mol Oncol. 2023 May;17(5):810-824. doi: 10.1002/1878-0261.13357. Epub 2022 Dec 29.
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Biomarker-Targeted Therapies in Non-Small Cell Lung Cancer: Current Status and Perspectives.生物标志物靶向治疗非小细胞肺癌:现状与展望。
Cells. 2022 Oct 12;11(20):3200. doi: 10.3390/cells11203200.
7
Artificial intelligence-based prediction of clinical outcome in immunotherapy and targeted therapy of lung cancer.基于人工智能的肺癌免疫治疗和靶向治疗临床结局预测。
Semin Cancer Biol. 2022 Nov;86(Pt 2):146-159. doi: 10.1016/j.semcancer.2022.08.002. Epub 2022 Aug 11.
8
Non-Small Cell Lung Cancer, Version 3.2022, NCCN Clinical Practice Guidelines in Oncology.非小细胞肺癌,2022年第3版,美国国立综合癌症网络(NCCN)肿瘤学临床实践指南
J Natl Compr Canc Netw. 2022 May;20(5):497-530. doi: 10.6004/jnccn.2022.0025.
9
The Clinically Actionable Molecular Profile of Early versus Late-Stage Non-Small Cell Lung Cancer, an Individual Age and Sex Propensity-Matched Pair Analysis.早晚期非小细胞肺癌的临床可操作分子谱:一项个体化年龄和性别倾向匹配分析。
Curr Oncol. 2022 Apr 11;29(4):2630-2643. doi: 10.3390/curroncol29040215.
10
Blood-based tumor mutational burden as a biomarker for atezolizumab in non-small cell lung cancer: the phase 2 B-F1RST trial.基于血液的肿瘤突变负担作为非小细胞肺癌中阿替利珠单抗的生物标志物:B-F1RST 期 2 试验。
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生物标志物检测在晚期非小细胞肺癌治疗中的重要性:播客

The Importance of Biomarker Testing in the Treatment of Advanced Non-Small Cell Lung Cancer: A Podcast.

作者信息

Hirsch Fred R, Kim Chul

机构信息

Icahn School of Medicine, Center for Thoracic Oncology, Tisch Cancer Center, Mount Sinai, New York, NY, USA.

Georgetown University, Washington, DC, USA.

出版信息

Oncol Ther. 2024 Jun;12(2):223-231. doi: 10.1007/s40487-024-00271-w. Epub 2024 Mar 27.

DOI:10.1007/s40487-024-00271-w
PMID:38536631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11187040/
Abstract

The identification of actionable biomarkers and development of targeted therapies have revolutionized the field of lung cancer treatment. In patients with advanced non-small cell lung cancer (NSCLC), biomarker testing can inform selection of effective targeted therapies as well as avoid therapies that are less likely to be effective in certain populations. A growing number of actionable targets, including those involving EGFR, ALK, ROS1, BRAF, MET, KRAS, NTRK, RET, HER2, and PD-L1, can be identified with biomarker testing. More than half of patients with advanced NSCLC have tumors that harbor genetic alterations that can be targeted. When these patients are treated with targeted therapy, survival and quality of life may be significantly improved. In addition, broad-based molecular testing may detect alterations identifying patients who are potentially eligible for current or future clinical trials. Comprehensive biomarker testing rates in communities are often low, and turnaround times for results can be unacceptably long. There is an unmet need for widespread, efficient, and routine testing of all biomarkers recommended by clinical guidelines. New testing techniques and technologies can make this an attainable goal. Panel-based sequencing platforms are becoming more accessible, and molecular biomarker analysis of circulating tumor DNA is becoming more common. In this podcast, we discuss the importance of biomarker testing in advanced NSCLC and explore topics such as testing methodologies, effect of biomarker testing on patient outcomes, emerging technologies, and strategies for improving testing rates in the United States. Supplementary file1 (MP4 121301 KB).

摘要

可操作生物标志物的识别以及靶向治疗的发展彻底改变了肺癌治疗领域。在晚期非小细胞肺癌(NSCLC)患者中,生物标志物检测可为有效靶向治疗的选择提供依据,同时避免在某些人群中不太可能有效的治疗方法。通过生物标志物检测可以识别越来越多的可操作靶点,包括那些涉及表皮生长因子受体(EGFR)、间变性淋巴瘤激酶(ALK)、原癌基因酪氨酸蛋白激酶ROS1(ROS1)、B-Raf原癌基因(BRAF)、间质上皮转化因子(MET)、 Kirsten大鼠肉瘤病毒癌基因(KRAS)、神经营养酪氨酸激酶受体(NTRK)、转染重排(RET)、人表皮生长因子受体2(HER2)和程序性死亡配体1(PD-L1)的靶点。超过一半的晚期NSCLC患者的肿瘤具有可靶向的基因改变。当这些患者接受靶向治疗时,生存和生活质量可能会显著提高。此外,广泛的分子检测可能会发现一些改变,从而识别出可能符合当前或未来临床试验条件的患者。社区中的综合生物标志物检测率通常较低,结果周转时间可能长得令人无法接受。对于临床指南推荐的所有生物标志物进行广泛、高效和常规检测的需求尚未得到满足。新的检测技术可以使这一目标得以实现。基于面板的测序平台越来越容易获得,循环肿瘤DNA的分子生物标志物分析也越来越普遍。在本播客中,我们讨论了生物标志物检测在晚期NSCLC中的重要性,并探讨了检测方法、生物标志物检测对患者预后的影响、新兴技术以及提高美国检测率的策略等主题。补充文件1(MP4 121301 KB)