Molecular alterations in non-small-cell lung cancer: perspective for targeted therapy and specimen management for the bronchoscopist

Respirology. 2014 Nov;19(8):1117-25. doi: 10.1111/resp.12377.

Abstract

Major advances have occurred over the past decade in our understanding of lung cancer pathobiology. Increasing knowledge of molecular aberrations in lung cancer, specifically the discovery of two driver genes in pharmacologically targetable tyrosine kinases involved in growth factor receptor signalling, epidermal growth factor receptor and anaplastic lymphoma kinase, has been of major therapeutic and prognostic importance. This discovery has allowed for new, personalized approach to the management of lung cancer. Recognizing the importance of molecular signatures of lung cancer, the College of American Pathologists, International Association for the Study of Lung Cancer and Association for Molecular Pathology released the first guidelines for molecular testing in lung cancer. The introduction of minimally invasive needle techniques for the evaluation of lung cancer patients, such as endobronchial ultrasound transbronchial needle aspiration and oesophageal ultrasound-fine-needle aspiration, has revolutionized the way lung cancer patients are assessed. Samples obtained using the minimally invasive needle approaches have been shown to be sufficient not only for routine molecular testing but also for multigenic analysis. This allows bronchoscopist to assume an increasingly important role in the diagnostic workup of patients with lung cancer at all stages of the disease and contribute to personalizing the care of lung cancer patients.

Keywords: anaplastic lymphoma kinase; endobronchial ultrasound transbronchial needle aspiration; epidermal growth factor receptor; lung cancer; oesophageal ultrasound-fine-needle aspiration.

Publication types

  • Review

MeSH terms

  • Anaplastic Lymphoma Kinase
  • Biopsy, Fine-Needle / methods
  • Bronchoscopy / methods
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Carcinoma, Non-Small-Cell Lung* / genetics
  • Carcinoma, Non-Small-Cell Lung* / pathology
  • ErbB Receptors / genetics*
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Lung Neoplasms* / pathology
  • Molecular Targeted Therapy / methods*
  • Pharmacogenetics
  • Prognosis
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Signal Transduction / drug effects

Substances

  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • ErbB Receptors
  • Receptor Protein-Tyrosine Kinases