Efficacy of Larotrectinib in <i>TRK</i> Fusion–Positive Cancers in Adults and Children

Alexander Drilon(Memorial Sloan Kettering Cancer Center), Theodore W. Laetsch(Memorial Sloan Kettering Cancer Center), Shivaani Kummar(Memorial Sloan Kettering Cancer Center), Steven G. DuBois(Memorial Sloan Kettering Cancer Center), Ulrik Lassen(Memorial Sloan Kettering Cancer Center), George D. Demetri(Memorial Sloan Kettering Cancer Center), Michael J. Nathenson(Memorial Sloan Kettering Cancer Center), Robert C. Doebele(Memorial Sloan Kettering Cancer Center), Anna F. Farago(Memorial Sloan Kettering Cancer Center), Alberto S. Pappo(St. Jude Children's Research Hospital), Brian Turpin(Cincinnati Children's Hospital Medical Center), Afshin Dowlati(Memorial Sloan Kettering Cancer Center), Marcia S. Brose(Memorial Sloan Kettering Cancer Center), Leo Mascarenhas(University of Southern California), Noah Federman(Memorial Sloan Kettering Cancer Center), Jordan Berlin(Memorial Sloan Kettering Cancer Center), Wafik S. El‐Deiry(Fox Chase Cancer Center), Christina S. Baik(Seattle Cancer Care Alliance), John F. Deeken(Memorial Sloan Kettering Cancer Center), Valentina Boni(Memorial Sloan Kettering Cancer Center), Ramamoorthy Nagasubramanian(Memorial Sloan Kettering Cancer Center), Matthew H. Taylor(Memorial Sloan Kettering Cancer Center), Erin R. Rudzinski(Seattle Children's Hospital), Funda Meric‐Bernstam(Memorial Sloan Kettering Cancer Center), Davendra Sohal(Cleveland Clinic), C. Patrick(West Virginia University), Luis E. Raez(Memorial Sloan Kettering Cancer Center), Jaclyn F. Hechtman(Memorial Sloan Kettering Cancer Center), Ryma Benayed(Memorial Sloan Kettering Cancer Center), Marc Ladanyi(Memorial Sloan Kettering Cancer Center), Brian B. Tuch(Memorial Sloan Kettering Cancer Center), Kevin Ebata(Memorial Sloan Kettering Cancer Center), Scott Cruickshank(Memorial Sloan Kettering Cancer Center), Nora Ku(Memorial Sloan Kettering Cancer Center), Michael C. Cox(Memorial Sloan Kettering Cancer Center), Douglas S. Hawkins(Seattle Children's Hospital), David S. Hong(Memorial Sloan Kettering Cancer Center), David M. Hyman(Memorial Sloan Kettering Cancer Center)
New England Journal of Medicine
February 21, 2018
Cited by 2,709Open Access
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Abstract

BACKGROUND: Fusions 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. METHODS: We 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. RESULTS: A 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. CONCLUSIONS: Larotrectinib 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 .).


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