An update on predictive biomarkers for treatment selection in non-small cell lung cancer

Tamkin Ahmadzada, Steven Kao, Glen Reid, Michael Boyer, Annabelle Mahar, Wendy A. Cooper

Research output: Contribution to journalArticlepeer-review

50 Citations (Scopus)

Abstract

It is now widely established that management of lung cancer is much more complex and cannot be centered on the binary classification of small-cell versus non-small cell lung cancer (NSCLC). Lung cancer is now recognized as a highly heterogeneous disease that develops from genetic mutations and gene expression patterns, which initiate uncontrolled cellular growth, proliferation and progression, as well as immune evasion. Accurate biomarker assessment to determine the mutational status of driver mutations such as EGFR, ALK and ROS1, which can be targeted by specific tyrosine kinase inhibitors, is now essential for treatment decision making in advanced stage NSCLC and has shifted the treatment paradigm of NSCLC to more individualized therapy. Rapid advancements in immunotherapeutic approaches to NSCLC treatment have been paralleled by development of a range of potential predictive biomarkers that can enrich for patient response, including PD-L1 expression and tumor mutational burden. Here, we review the key biomarkers that help predict response to treatment options in NSCLC patients.
Original languageEnglish
Article number153
Number of pages12
JournalJournal of Clinical Medicine
Volume7
Issue number6
DOIs
Publication statusPublished - 2018

Open Access - Access Right Statement

© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Keywords

  • biochemical markers
  • cancer
  • immunotherapy
  • lungs
  • protein, tyrosine kinase
  • receptors

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