%A Tran,Phu N. %A Klempner,Samuel J. %D 2016 %J Frontiers in Medicine %C %F %G English %K Alectinib,NSCLC,ALK,Second line,crizotinib,Resistance %Q %R 10.3389/fmed.2016.00065 %W %L %M %P %7 %8 2016-November-30 %9 Mini Review %+ Samuel J. Klempner,The Angeles Clinic and Research Institute,USA,sklempner@partners.org %+ Samuel J. Klempner,Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute,USA,sklempner@partners.org %# %! Alectinib for second line NSCLC %* %< %T Focus on Alectinib and Competitor Compounds for Second-Line Therapy in ALK-Rearranged NSCLC %U https://www.frontiersin.org/articles/10.3389/fmed.2016.00065 %V 3 %0 JOURNAL ARTICLE %@ 2296-858X %X The management of anaplastic lymphoma kinase rearranged (ALK+) non-small cell lung cancer (NSCLC) exemplifies the potential of a precision medicine approach to cancer care. The ALK inhibitor crizotinib has led to improved outcomes in the first- and second-line setting; however, toxicities, intracranial activity, and acquired resistance necessitated the advent of later generation ALK inhibitors. A large portion of acquired resistance to ALK inhibitors is caused by secondary mutations in the ALK kinase domain. Alectinib is a second-generation ALK inhibitor capable of overcoming multiple crizotinib-resistant ALK mutations and has demonstrated improved outcomes after crizotinib failure. Favorable toxicity profile and improved intracranial activity have spurred ongoing front-line trials and comparisons to other ALK inhibitors. However, important questions regarding comparability to competitor compounds, acquired alectinib resistance, and ALK inhibitor sequencing remain. Here, we review the key clinical data supporting alectinib in the second-line therapy of ALK+ NSCLC and provide context in comparison to other ALK inhibitors in development.