| Literature DB >> 32677452 |
Tanios S Bekaii-Saab1, Juan W Valle2, Eric Van Cutsem3, Lorenza Rimassa4,5, Junji Furuse6, Tatsuya Ioka7, Davide Melisi8, Teresa Macarulla9, John Bridgewater10, Harpreet Wasan11, Mitesh J Borad1, Ghassan K Abou-Alfa12,13, Ping Jiang14, Christine F Lihou14, Huiling Zhen14, Ekaterine Asatiani15, Luis Féliz15, Arndt Vogel16.
Abstract
FGFR2 rearrangements resulting in dysregulated signaling are drivers of cholangiocarcinoma (CCA) tumorigenesis, and occur almost exclusively in intrahepatic CCA. Pemigatinib, a selective, potent, oral inhibitor of FGFR1-3, has demonstrated efficacy and safety in a Phase II study of patients with previously treated locally advanced/metastatic CCA harboring FGFR2 fusions/rearrangements. We describe the study design of FIGHT-302, an open-label, randomized, active-controlled, multicenter, global, Phase III study comparing the efficacy and safety of first-line pemigatinib versus gemcitabine plus cisplatin in patients with advanced CCA with FGFR2 rearrangements (NCT03656536). The primary end point is progression-free survival; secondary end points are objective response rate, overall survival, duration of response, disease control rate, safety and quality of life. Clinical Trial Registration: NCT03656536 (ClinicalTrials.gov).Entities:
Keywords: FGFR; INCB054828; cholangiocarcinoma; pemigatinib
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Year: 2020 PMID: 32677452 DOI: 10.2217/fon-2020-0429
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404