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肺腺癌的分子遗传学检测:临床相关突变和易位的实用方法。

Molecular genetic testing for lung adenocarcinomas: a practical approach to clinically relevant mutations and translocations.

出版信息

J Clin Pathol. 2013 Oct;66(10):870-4. doi: 10.1136/jclinpath-2012-201336. Epub 2013 Jun 25.

Abstract

There is a consensus that molecular testing of the lung carcinoma should be the standard of care in the clinical management of patients with lung carcinoma. Recent practice guidelines in oncology and pathology recommend that all advanced and metastatic non-small-cell lung carcinoma with adenocarcinoma histology undergo biomarker testing for epidermal growth factor receptor gene (EGFR) mutations and anaplastic lymphoma kinase gene (ALK) rearrangements. Other types of non-small-cell carcinoma may be considered for such testing if they occur in never-smokers. The landscape of targetable biomarkers in non-small-cell carcinoma is changing rapidly, and demand for clinical testing beyond EGFR mutations and ALK gene rearrangements is increasing. Many patients may test positive for other 'drivers'. As a result, they may be treated with approved biomarker-driven therapies or may be eligible to receive investigational agents in clinical trials. This creates challenges for treating physicians and pathologists such as obtaining sufficient tissue for molecular testing and standardisation of molecular testing in clinical laboratories. This review will focus on the most important lung carcinoma biomarkers predictive of response and will discuss proposed routine molecular testing in clinical practice.

摘要

人们普遍认为,肺癌的分子检测应该成为肺癌临床管理的标准。肿瘤学和病理学的最新实践指南建议,所有具有腺癌组织学的晚期和转移性非小细胞肺癌都应进行表皮生长因子受体基因 (EGFR) 突变和间变性淋巴瘤激酶基因 (ALK) 重排的生物标志物检测。如果从未吸烟者中发生其他类型的非小细胞癌,则可能考虑进行此类检测。非小细胞癌中可靶向生物标志物的格局正在迅速变化,对 EGFR 突变和 ALK 基因重排以外的临床检测的需求正在增加。许多患者可能对其他“驱动因素”呈阳性。因此,他们可能会接受批准的生物标志物驱动的治疗,或者有资格在临床试验中接受研究药物。这给治疗医生和病理学家带来了挑战,例如获得足够的组织进行分子检测以及临床实验室中分子检测的标准化。这篇综述将重点介绍预测反应的最重要的肺癌生物标志物,并讨论在临床实践中建议进行的常规分子检测。

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