Safety and Antitumor Activity of the Multitargeted Pan-TRK, ROS1, and ALK Inhibitor Entrectinib: Combined Results from Two Phase I Trials (ALKA-372-001 and STARTRK-1)
Memorial Sloan Kettering Cancer Center · Cornell University · +19 more institutions
Abstract
Abstract Entrectinib, a potent oral inhibitor of the tyrosine kinases TRKA/B/C, ROS1, and ALK, was evaluated in two phase I studies in patients with advanced or metastatic solid tumors, including patients with active central nervous system (CNS) disease. Here, we summarize the overall safety and report the antitumor activity of entrectinib in a cohort of patients with tumors harboring NTRK1/2/3, ROS1, or ALK gene fusions, naïve to prior TKI treatment targeting the specific gene, and who were treated at doses that achieved therapeutic exposures consistent with the recommended phase II dose. Entrectinib was well tolerated, with predominantly Grades 1/2 adverse events that were reversible with dose modification.…
Citation impact
- FWCI
- 76.51
- Percentile
- 100%
- References
- 44
Authors
35- ADAlexander DrilonCorresponding
Memorial Sloan Kettering Cancer Center, Cornell University, Kettering University
- SSSalvatore Siena
University of Milan, Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
- SISai‐Hong Ignatius Ou
Comprehensive Blood & Cancer Center
- MRManish R. Patel
Sarah Cannon, Florida Cancer Specialists & Research Institute
- MAMyung‐Ju Ahn
Seoul Medical Center, Bristol-Myers Squibb (South Korea)
Topics & keywords
- ROS1
- Cancer
- Medicine
- Cancer research
- ALK inhibitor
- Trk receptor
- Crizotinib
- Lung cancer
- Good health and well-being