Path Less Traveled: Targeting Rare Driver Oncogenes in Non–Small-Cell Lung Cancer

Author:

Lim Sun Min1,Lee Jii Bum1ORCID,Oya Yuko2,Nutzinger Jorn3,Soo Ross3ORCID

Affiliation:

1. Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea

2. Department of Respiratory Disease, Fujita Health University, Toyoake, Japan

3. Department of Haematology-Oncology, National University Cancer Institute, Singapore

Abstract

Over the past decade, tremendous efforts have been made in the development of targeted agents in non–small-cell lung cancer (NSCLC) with nonsquamous histology. Pivotal studies have used next-generation sequencing to select the patient population harboring oncogenic driver alterations that are targetable with targeted therapies. As treatment paradigm rapidly evolves for patients with rare oncogene-driven NSCLC, updated comprehensive overview of diagnostic approach and treatment options is paramount in clinical settings. In this review article, we discuss the epidemiology, molecular testing, and landmark clinical trials addressing the targeted agents for ROS1 rearrangement, METex14 skipping mutation, EGFR exon 20 insertion, KRAS G12C mutation, HER2 mutation, RET fusion, NTRK fusion, and BRAF mutations.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Oncology (nursing),Health Policy,Oncology

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