Suppr超能文献

表皮生长因子受体突变在东亚非小细胞肺癌患者中的分析的临床和检测方案:一种联合临床-分子病理方法。

Clinical and testing protocols for the analysis of epidermal growth factor receptor mutations in East Asian patients with non-small cell lung cancer: a combined clinical-molecular pathological approach.

机构信息

Department of Pathology, National University Health System, Cancer Science Institute of Singapore, National University of Singapore, Singapore.

出版信息

J Thorac Oncol. 2011 Oct;6(10):1663-9. doi: 10.1097/JTO.0b013e318227816a.

Abstract

BACKGROUND

Several randomized phase III studies in advanced stage non-small cell lung cancer (NSCLC) confirmed the superior response rate and progression-free survival of using epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor as first-line therapy compared with chemotherapy in patients with activating EGFR mutations. Despite the need for EGFR mutation tests to guide first-line therapy in East Asian NSCLC, there are no current standard clinical and testing protocols.

METHODS

A consensus meeting was held involving expert oncologists, pulmonologists, and pathologists to discuss the current status and variations in EGFR mutation testing of NSCLC across Asia and to recommend a standard clinical and laboratory testing approach for future use.

RESULTS

Currently, EGFR mutation tests are only routinely performed in some East Asian countries and medical centers. The consensus recommendation was to perform the test in all newly diagnosed patients with advanced stage nonsquamous lung cancer and some squamous patients with clinical features associated with higher prevalence of EGFR mutations. To increase the sensitivity and specificity of the EGFR mutation tests, tissue acquisition and pretest sample evaluation are important steps in addition to standardization of the EGFR mutation test methodology.

CONCLUSION

A standardized EGFR mutation testing protocol is an essential step toward realization of personalized medicine in East Asian NSCLC treatment.

摘要

背景

几项针对晚期非小细胞肺癌(NSCLC)的随机 III 期研究证实,与化疗相比,具有激活表皮生长因子受体(EGFR)突变的患者使用 EGFR 酪氨酸激酶抑制剂作为一线治疗可提高反应率和无进展生存期。尽管需要进行 EGFR 突变检测来指导东亚 NSCLC 的一线治疗,但目前尚无标准的临床和检测方案。

方法

举行了一次共识会议,涉及肿瘤学家、肺科专家和病理学家,讨论了亚洲各地 NSCLC 的 EGFR 突变检测的现状和差异,并为未来推荐了一种标准的临床和实验室检测方法。

结果

目前,EGFR 突变检测仅在一些东亚国家和医疗中心常规进行。共识建议对所有晚期非鳞状肺癌新诊断患者以及某些具有较高 EGFR 突变发生率相关临床特征的鳞状患者进行检测。为了提高 EGFR 突变检测的敏感性和特异性,除了 EGFR 突变检测方法的标准化外,组织采集和检测前样本评估也是重要步骤。

结论

标准化的 EGFR 突变检测方案是实现东亚 NSCLC 治疗个体化医学的重要步骤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验