| Literature DB >> 25689095 |
Nesaretnam Barr Kumarakulasinghe1, Nico van Zanwijk, Ross A Soo.
Abstract
Historically, patients with advanced stage non-small cell lung cancer (NSCLC) were treated with chemotherapy alone, but a therapeutic plateau has been reached. Advances in the understanding of molecular genetics have led to the recognition of multiple molecularly distinct subsets of NSCLC. This in turn has led to the development of rationally directed molecular targeted therapy, leading to improved clinical outcomes. Tumour genotyping for EGFR mutations and ALK rearrangement has meant chemotherapy is no longer given automatically as first-line treatment but reserved for when patients do not have a 'druggable' driver oncogene. In this review, we will address the current status of clinically relevant driver mutations and emerging new molecular subsets in lung adenocarcinoma and squamous cell carcinoma, and the role of targeted therapy and mechanisms of acquired resistance to targeted therapy.Entities:
Keywords: anaplastic lymphoma kinase; epidermal growth factor receptor; molecular targeted therapy; non-small cell lung cancer
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Year: 2015 PMID: 25689095 DOI: 10.1111/resp.12490
Source DB: PubMed Journal: Respirology ISSN: 1323-7799 Impact factor: 6.424