Response to Dabrafenib Plus Trametinib in a Patient With an Uncommon Activating BRAF Mutation: A First in Non-Small Cell Lung Cancer

J Natl Compr Canc Netw. 2024 Mar 13;22(3):e247009. doi: 10.6004/jnccn.2024.7009.

Abstract

Mutations in BRAF are present in 4% of non-small cell lung cancer (NSCLC), of which half are well-characterized activating variants affecting codon 600 (classified as class I). These mutations, most commonly BRAF V600E, have been associated with response to BRAF/MEK-directed small molecule kinase inhibitors. NSCLC with kinase-activating BRAF mutations occurring at other codons (class II variants) represent a substantial portion of BRAF-mutated NSCLC, but use of targeted therapy in these tumors is still under investigation. Class II mutations have been described in other tumor types and have been associated with response to BRAF/MEK-targeted agents, although optimal treatment strategies for these patients are lacking. This report presents a case of a woman with metastatic NSCLC harboring a class II BRAF p.N486_P490del variant who had a sustained clinical response to combination therapy with dabrafenib and trametinib. This first report of the use of BRAF/MEK-targeted therapy for this variant in NSCLC supports consideration of such treatment for tumors with class II BRAF variants.

Publication types

  • Case Reports

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Carcinoma, Non-Small-Cell Lung* / genetics
  • Carcinoma, Non-Small-Cell Lung* / pathology
  • Female
  • Humans
  • Imidazoles*
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Lung Neoplasms* / pathology
  • MAP Kinase Kinase Kinases
  • Mitogen-Activated Protein Kinase Kinases / genetics
  • Mutation
  • Oximes / therapeutic use
  • Proto-Oncogene Proteins B-raf / genetics
  • Pyridones*
  • Pyrimidinones*

Substances

  • trametinib
  • dabrafenib
  • Proto-Oncogene Proteins B-raf
  • Oximes
  • MAP Kinase Kinase Kinases
  • Mitogen-Activated Protein Kinase Kinases
  • BRAF protein, human
  • Imidazoles
  • Pyridones
  • Pyrimidinones