| Literature DB >> 27330348 |
B Melosky1, J Agulnik2, R Albadine2, S Banerji3, D G Bebb4, D Bethune5, N Blais2, C Butts4, P Cheema6, P Cheung6, V Cohen2, J Deschenes4, D N Ionescu1, R Juergens6, S Kamel-Reid6, S A Laurie1, G Liu1, W Morzycki5, M S Tsao6, Z Xu5, V Hirsh2.
Abstract
Anaplastic lymphoma kinase (alk) is an oncogenic driver in non-small-cell lung cancer (nsclc). Chromosomal rearrangements involving the ALK gene occur in up to 4% of nonsquamous nsclc patients and lead to constitutive activation of the alk signalling pathway. ALK-positive nsclc is found in relatively young patients, with a median age of 50 years. Patients frequently have brain metastasis. Targeted inhibition of the alk pathway prolongs progression-free survival in patients with ALK-positive advanced nsclc. The results of several recent clinical trials confirm the efficacy and safety benefit of crizotinib and ceritinib in this population. Canadian oncologists support the following consensus statement: All patients with advanced nonsquamous nsclc (excluding pure neuroendocrine carcinoma) should be tested for the presence of an ALK rearrangement. If an ALK rearrangement is present, treatment with a targeted alk inhibitor in the first-line setting is recommended. As patients become resistant to first-generation alk inhibitors, other treatments, including second-generation alk inhibitors can be considered.Entities:
Keywords: ALK; anaplastic lymphoma kinase; molecular testing; non-small-cell lung cancer; targeted inhibition
Year: 2016 PMID: 27330348 PMCID: PMC4900831 DOI: 10.3747/co.23.3120
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677