Efficacy of Larotrectinib inTRKFusion–Positive Cancers in Adults and Children

Autor: Steven G. DuBois, Michael J. Nathenson, John F. Deeken, Anna F. Farago, Luis E. Raez, Alberto S. Pappo, Ryma Benayed, Alexander Drilon, Funda Meric-Bernstam, Christina S. Baik, Brian B. Tuch, David M. Hyman, Valentina Boni, Noah Federman, Marcia S. Brose, Ulrik Lassen, Douglas S. Hawkins, Kevin Ebata, Nora Ku, Jordan Berlin, Scott Cruickshank, Leo Mascarenhas, Theodore W. Laetsch, Brian Turpin, George D. Demetri, Afshin Dowlati, Patrick C. Ma, Shivaani Kummar, David S. Hong, Robert C. Doebele, Jaclyn F. Hechtman, Ramamoorthy Nagasubramanian, Davendra Sohal, Matthew H. Taylor, Michael C. Cox, Wafik S. El-Deiry, Marc Ladanyi, Erin R. Rudzinski
Rok vydání: 2018
Předmět:
Male
0301 basic medicine
Oncology
Oncogene Proteins
Fusion

Phases of clinical research
Entrectinib
Kaplan-Meier Estimate
Medical and Health Sciences
0302 clinical medicine
Overall response rate
Neoplasms
Clinical endpoint
Young adult
Child
Cancer
Oncogene Proteins
Pediatric
General Medicine
Middle Aged
Highly selective
Editorial Commentary
Child
Preschool

6.1 Pharmaceuticals
030220 oncology & carcinogenesis
Female
Patient Safety
Adult
medicine.medical_specialty
Adolescent
Antineoplastic Agents
Disease-Free Survival
Young Adult
03 medical and health sciences
Clinical Research
General & Internal Medicine
Internal medicine
medicine
Humans
Fusion
Preschool
Aged
business.industry
Receptor Protein-Tyrosine Kinases
Infant
Evaluation of treatments and therapeutic interventions
Clinical trial
Pyrimidines
030104 developmental biology
Trk receptor
Pyrazoles
business
Protein Kinases
Zdroj: The New England journal of medicine, vol 378, iss 8
ISSN: 1533-4406
0028-4793
DOI: 10.1056/nejmoa1714448
Popis: BackgroundFusions involving one of three tropomyosin receptor kinases (TRK) occur in diverse cancers in children and adults. We evaluated the efficacy and safety of larotrectinib, a highly selective TRK inhibitor, in adults and children who had tumors with these fusions.MethodsWe enrolled patients with consecutively and prospectively identified TRK fusion-positive cancers, detected by molecular profiling as routinely performed at each site, into one of three protocols: a phase 1 study involving adults, a phase 1-2 study involving children, or a phase 2 study involving adolescents and adults. The primary end point for the combined analysis was the overall response rate according to independent review. Secondary end points included duration of response, progression-free survival, and safety.ResultsA total of 55 patients, ranging in age from 4 months to 76 years, were enrolled and treated. Patients had 17 unique TRK fusion-positive tumor types. The overall response rate was 75% (95% confidence interval [CI], 61 to 85) according to independent review and 80% (95% CI, 67 to 90) according to investigator assessment. At 1 year, 71% of the responses were ongoing and 55% of the patients remained progression-free. The median duration of response and progression-free survival had not been reached. At a median follow-up of 9.4 months, 86% of the patients with a response (38 of 44 patients) were continuing treatment or had undergone surgery that was intended to be curative. Adverse events were predominantly of grade 1, and no adverse event of grade 3 or 4 that was considered by the investigators to be related to larotrectinib occurred in more than 5% of patients. No patient discontinued larotrectinib owing to drug-related adverse events.ConclusionsLarotrectinib had marked and durable antitumor activity in patients with TRK fusion-positive cancer, regardless of the age of the patient or of the tumor type. (Funded by Loxo Oncology and others; ClinicalTrials.gov numbers, NCT02122913 , NCT02637687 , and NCT02576431 .).
Databáze: OpenAIRE