NYMC Faculty Publications
Novel ALK Inhibitors in Clinical Use and Development
Author Type(s)
Faculty
DOI
10.1186/s13045-015-0122-8
Journal Title
Journal of Hematology & Oncology
First Page
17
Document Type
Article
Publication Date
2-27-2015
Abstract
Anaplastic lymphoma kinase 1 (ALK-1) is a member of the insulin receptor tyrosine kinase family. ALK-1 was initially found in anaplastic large cell lymphoma (ALCL). ALK mutations have also been implicated in the pathogenesis of non-small cell lung cancer (NSCLC) and other solid tumors. Multiple small molecule inhibitors with activity against ALK and related oncoproteins are under clinical development. Two of them, crizotinib and ceritinib, have been approved by FDA for treatment of locally advanced and metastatic NSCLC. More agents (alectinib, ASP3026, X396) with improved safety, selectivity, and potency are in the pipeline. Dual inhibitors targeting ALK and EGFRm (AP26113), TRK (TSR011), FAK (CEP-37440), or ROS1 (RXDX-101, PF-06463922) are under active clinical development.
Recommended Citation
Iragavarapu, C., Mustafa, M., Akinleye, A., Furqan, M., Mittal, V., Cang, S., & Liu, D. (2015). Novel ALK Inhibitors in Clinical Use and Development. Journal of Hematology & Oncology, 8, 17. https://doi.org/10.1186/s13045-015-0122-8