RET-rearranged non-small-cell lung cancer and therapeutic implications

Intern Med J. 2019 Dec;49(12):1541-1545. doi: 10.1111/imj.14654.

Abstract

First-line tyrosine kinase inhibitors are standard of care for non-small-cell lung cancers (NSCLC) harbouring an epidermal growth factor receptor mutation, anaplastic lymphoma kinase fusion or c-ros oncogene 1 rearrangement. Other targetable oncogenic drivers have been identified but testing for these is neither funded nor commonly performed in Australia. Using a case example, we discuss the importance of considering several other genomic aberrations in our population, such as rearrangements in the RET proto-oncogene, which occur in 1-2% of lung adenocarcinoma. New oncogenic drivers and corresponding targeted agents are constantly being discovered; these will continue to refine the treatment of non-small-cell lung cancer in the era of precision medicine.

Keywords: RET rearrangement; genomic profiling; non-small-cell lung cancer; tyrosine kinase inhibitor; vandetanib.

Publication types

  • Case Reports

MeSH terms

  • Australia
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Female
  • Gene Rearrangement
  • Genetic Predisposition to Disease
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics*
  • Middle Aged
  • Mutation
  • Piperidines
  • Precision Medicine
  • Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-ret / genetics*
  • Quinazolines

Substances

  • MAS1 protein, human
  • Piperidines
  • Proto-Oncogene Mas
  • Quinazolines
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-ret
  • RET protein, human
  • vandetanib