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处理 NSCLC EGFR 突变检测和治疗:意大利真实世界视角的全面综述。

Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective.

机构信息

Department of Public Health, University of Naples Federico II, 80131, Naples, Italy.

U.O.C. of Oncology, Azienda Ospedaliera Universitaria Integrata, University of Verona, Verona, Italy.

出版信息

Crit Rev Oncol Hematol. 2021 Apr;160:103300. doi: 10.1016/j.critrevonc.2021.103300. Epub 2021 Mar 17.

DOI:10.1016/j.critrevonc.2021.103300
PMID:33744362
Abstract

Since their discovery, relevant efforts have been made to optimize the detection approaches to EGFR mutations as well as the clinical management of EGFR-mutated NSCLC. The recent shift from single gene testing to novel comprehensive detection platforms along with the development of new generation tyrosine kinase inhibitors, targeting both common and uncommon EGFR-mutations, is leading to a progressive increase in the number of patients who may benefit from targeted approaches, with subsequent impact on their long-term survival and quality of life. However, a prompt and adequate implementation of the most recent diagnostic and treatment advances in the routine practice often remains critical to be specifically addressed. In this review we provide a complete and updated overview of the different detection platforms and therapeutic options currently available for the clinical management of advanced EGFR-positive NSCLC, summarizing scientific evidence and describing molecular testing as well as treatment practice in the real-word scenario.

摘要

自发现以来,人们一直致力于优化 EGFR 突变的检测方法以及 EGFR 突变型 NSCLC 的临床管理。最近,从单一基因检测到新型综合检测平台的转变,以及针对常见和不常见 EGFR 突变的新一代酪氨酸激酶抑制剂的发展,导致可能受益于靶向治疗的患者数量不断增加,从而对他们的长期生存和生活质量产生影响。然而,在常规实践中及时、充分地实施最新的诊断和治疗进展仍然是需要特别关注的关键问题。在这篇综述中,我们全面、及时地概述了目前可用于晚期 EGFR 阳性 NSCLC 临床管理的不同检测平台和治疗选择,总结了科学证据,并描述了实际情况下的分子检测和治疗实践。

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