Future Perspectives in Detecting EGFR and ALK Gene Alterations in Liquid Biopsies of Patients with NSCLC

Int J Mol Sci. 2021 Apr 7;22(8):3815. doi: 10.3390/ijms22083815.

Abstract

Non-small-cell lung cancer (NSCLC) is a major cause of death worldwide. Alterations in such genes as EGFR and ALK are considered important biomarkers in NSCLC due to the existence of targeted therapies with specific tyrosine kinase inhibitors (TKIs). However, specific resistance-related mutations can occur during TKI treatment, which often result in therapy inefficacy. Liquid biopsies arise as a reliable tool for the early detection of these types of alterations, allowing a non-invasive follow-up of the patients. Furthermore, they can be essential for cancer screening, initial diagnosis and to check surgery success. Despite the great advantages of liquid biopsies in NSCLC and the high input that next-generation sequencing (NGS) approaches can provide in this field, its use in oncology is still limited. With improvement of assay sensitivity and the establishment of clinical guidelines for liquid biopsy analysis, it is expected that they will be used in routine procedures. This review focuses on the usefulness of liquid biopsies of NSCLC patients as a means to detect alterations in EGFR and ALK genes and in disease management, highlighting the impact of NGS methods.

Keywords: ALK; EGFR; liquid biopsies; next-generation sequencing; non-small-cell lung cancer; predictive biomarkers.

Publication types

  • Review

MeSH terms

  • Anaplastic Lymphoma Kinase / genetics*
  • Biomarkers, Tumor
  • Biopsy
  • Carcinoma, Non-Small-Cell Lung / diagnosis*
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Diagnostic Tests, Routine
  • Drug Resistance, Neoplasm / genetics
  • ErbB Receptors / genetics
  • Humans
  • Immunohistochemistry
  • Liquid Biopsy / methods*
  • Liquid Biopsy / standards
  • Lung Neoplasms / diagnosis*
  • Lung Neoplasms / genetics*
  • Molecular Diagnostic Techniques / methods
  • Molecular Diagnostic Techniques / standards
  • Mutation
  • Oncogene Proteins, Fusion / genetics
  • Prognosis

Substances

  • Biomarkers, Tumor
  • Oncogene Proteins, Fusion
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • EGFR protein, human
  • ErbB Receptors