Entrectinib for the treatment of metastatic NSCLC: safety and efficacy.
Andrea Sartore-BianchiElio Gregory PizzutiloGiovanna MarrapeseFederica TosiGiulio CereaSalvatore SienaPublished in: Expert review of anticancer therapy (2020)
Introduction: Gene fusions are strong driver alterations in various cancers, increasingly diagnosed with multiple testing techniques. ROS1 fusions can be found in 1-2% of non-small cell lung cancer (NSCLC) and several tyrosine kinase inhibitors (TKIs) have been tested in this oncogene-driven disease. NTRK fusions are characteristic of a few rare types of cancer, also infrequently seen in some common cancers including NSCLC. Entrectinib is a newer ROS1 and NTRK inhibitor developed across different tumor types harboring rearrangements in these genes. Entrectinib was granted FDA accelerated approval in August 2019 for the treatment of ROS1+ NSCLC and NTRK-driven solid tumors.Areas covered: This review covers the mechanism of action, safety, and efficacy of entrectinib in patients with metastatic NSCLC.Expert opinion: Entrectinib is an orally bioavailable TKI of TrkA, TrkB, TrkC, and ROS1, with the ability to cross the blood-brain barrier. Entrectinib was effective and well-tolerated in patients harboring ROS1- or NTRK-rearranged NSCLC treated within phase I and II studies. Entrectinib appears to be the most appropriate treatment choice for TKIs-naïve patients, especially in those presenting brain metastasis. Conversely, in case of systemic progression with the evidence of acquired resistance mutations in ROS1 or Trk proteins, a sequential therapy with entrectinib could not be successful.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- cell death
- dna damage
- reactive oxygen species
- newly diagnosed
- end stage renal disease
- ejection fraction
- brain metastases
- squamous cell carcinoma
- stem cells
- multiple sclerosis
- combination therapy
- tyrosine kinase
- epidermal growth factor receptor
- white matter
- gene expression
- brain injury
- blood brain barrier
- mesenchymal stem cells
- papillary thyroid
- resting state
- functional connectivity
- childhood cancer