Abstract
The discovery of anaplastic lymphoma kinase (ALK) gene rearrangements and the development of tyrosine kinase inhibitors (TKI) that target them have achieved unprecedented success in the management of patients with ALK-positive non-small cell lung cancer (NSCLC). Despite the high efficacy of crizotinib, the first oral ALK TKI approved for the treatment of ALK-positive NSCLC, almost all patients inevitably develop acquired resistance, showing disease progression in the brain or in other parenchymal sites. Second- or third-generation ALK TKIs have shown to be active in crizotinib-pretreated or crizotinib-naïve ALK-positive patients, even in those with brain metastases. In this review, the current knowledge regarding ALK-positive NSCLC, focusing on the biology of the disease and the available therapeutic options are discussed.
Original language | English |
---|---|
Pages (from-to) | 6361-6376 |
Number of pages | 16 |
Journal | OncoTargets and Therapy |
Volume | 9 |
DOIs | |
Publication status | Published - Oct 17 2016 |
Keywords
- Alectinib
- ALK
- Brain metastases
- Brigatinib
- Ceritinib
- Crizotinib
- Lorlatinib
- NSCLC
ASJC Scopus subject areas
- Oncology
- Pharmacology (medical)