1. TRTH-10. PEDIATRIC PHASE 1/1B STUDY OF ENTRECTINIB IN PATIENTS WITH PRIMARY BRAIN TUMORS, NEUROBLASTOMA, AND NTRK, ROS1, OR ALK FUSIONS
- Author
-
Sunitha Rangaraju, Pratik S. Multani, Edna Chow Maneval, Vanessa Esquibel, Zachary Hornby, Gang Li, and Jason Christiansen
- Subjects
Cancer Research ,business.industry ,Cancer ,Entrectinib ,medicine.disease ,Dysgeusia ,03 medical and health sciences ,Abstracts ,0302 clinical medicine ,Oncology ,030220 oncology & carcinogenesis ,Neuroblastoma ,Cancer research ,medicine ,ROS1 ,Anaplastic lymphoma kinase ,Neurology (clinical) ,medicine.symptom ,business ,Infantile Fibrosarcoma ,Tyrosine kinase ,030217 neurology & neurosurgery - Abstract
The STARTRK-NG (Studies of Tumor Alterations Responsive to Targeting Receptor Kinases - Next Generation) trial is a Phase 1/1b study of entrectinib in pediatric patients with cancer, including primary brain tumors, neuroblastoma, and other non-neuroblastoma, extracranial solid tumors harboring NTRK, ROS1, or ALK gene fusions (NCT02650401). Entrectinib is a potent oral, CNS-penetrant, inhibitor of the tyrosine kinases TRKA/B/C (encoded by the genes NTRK1/2/3, respectively), ROS1, and ALK with IC50s < 2 nM (biochemical kinase assay). Overall, gene fusions are rare in the cancer population (10% incidence) treatment-related adverse events have been fatigue/asthenia, dysgeusia, paresthesia, nausea, myalgia, diarrhea, dizziness, arthralgia, vomiting, and constipation; importantly, there has been no evidence of cumulative toxicity. In addition, we have treated a 20-month-old boy presenting with infantile fibrosarcoma metastatic to the brain, which harbored an ETV6-NTRK3 fusion. Tumor restaging following 1 month of therapy showed a significant tumor regression of CNS metastases accompanied by significant clinical improvement. Together, these data provide compelling evidence to identify pediatric patients harboring NTRK, ROS1, or ALK fusions for enrollment in the STARTRK-NG trial.
- Published
- 2017