Podcast on Lorlatinib as a First-Line Treatment Option for Patients with ALK-Positive Metastatic NSCLC with Brain Metastasis.
Geoffrey LiuVincent K LamPublished in: Advances in therapy (2023)
Brain metastases are especially common in anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC), with a cumulative incidence of over 50% and associated with a poor prognosis, high symptom burden, and decreased quality of life. Lorlatinib is a brain-penetrant, third-generation ALK tyrosine kinase inhibitor (TKI), which has a high potency against resistance mutations seen with earlier generation ALK TKIs. In 2018, lorlatinib was granted accelerated approval in second- and third-line treatment for use in patients with ALK-positive metastatic NSCLC on the basis of phase 1/2 study results. This initial approval was expanded for first-line treatment of patients with ALK-positive metastatic NSCLC on the basis of the interim analysis of the phase 3 CROWN study showing longer progression-free survival, time to intracranial progression, duration of response, and objective response rate compared with crizotinib. This manuscript is a transcript of our podcast, in which we discuss the clinical significance of controlling the onset of brain metastases, considerations in selecting a first-line therapy option, efficacy and safety observed in patients with and without brain metastases, and rationales for using lorlatinib upfront versus reserving for a later line in therapy.
Keyphrases
- brain metastases
- small cell lung cancer
- advanced non small cell lung cancer
- poor prognosis
- epidermal growth factor receptor
- squamous cell carcinoma
- free survival
- long non coding rna
- tyrosine kinase
- risk factors
- white matter
- resting state
- stem cells
- diffuse large b cell lymphoma
- rna seq
- clinical trial
- mesenchymal stem cells
- cerebral ischemia
- replacement therapy
- functional connectivity
- protein kinase