医学
癌症
融合
肿瘤科
内科学
数学
哲学
语言学
作者
Alison M. Schram,Kōichi Goto,Dong-Wan Kim,Teresa Macarulla,Antoine Hollebecque,Eileen M. O’Reilly,Sai‐Hong Ignatius Ou,Jordi Rodón,Sun Young Rha,Kazumi Nishino,M. Duruisseaux,Joon Oh Park,Cindy Neuzillet,Stephen V. Liu,Benjamin A. Weinberg,James M. Cleary,Emiliano Calvo,Kumiko Umemoto,Misako Nagasaka,Christoph Springfeld
标识
DOI:10.1056/nejmoa2405008
摘要
BACKGROUND: fusion-positive solid tumors are unclear. METHODS: fusion-positive cancer involving any tumor type to receive zenocutuzumab at a dose of 750 mg intravenously every 2 weeks. The primary end point was overall response (complete or partial response) according to investigator assessment. Secondary end points included duration of response, progression-free survival, and safety. RESULTS: fusion partners. The median progression-free survival was 6.8 months (95% CI, 5.5 to 9.1). Adverse events were primarily grade 1 or 2. The most common adverse events that were considered by the investigator to be related to zenocutuzumab were diarrhea (in 18% of the patients), fatigue (in 12%), and nausea (in 11%). Infusion-related reactions (composite term) were observed in 14% of the patients. One patient discontinued zenocutuzumab owing to a treatment-related adverse event. CONCLUSIONS: fusion-positive cancer, notably NSCLC and pancreatic cancer, with mainly low-grade adverse events. (Funded by Merus; eNRGy ClinicalTrials.gov number, NCT02912949.).
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