Arndt Vogel
阿恩特·福格尔
MD
Professor of Gastroenterology and Hepatology; Clinician-Scientist, Division of Gastroenterology, University Health Network, Toronto; Formerly Professor, Hannover Medical School胃肠病与肝病学教授,多伦多大学卫生网络胃肠科医学科学家
👥Biography 个人简介
Arndt Vogel, MD is a Professor of Gastroenterology and Hepatology who has worked at Hannover Medical School (Germany) and, most recently, at the University of Toronto/University Health Network, where he continues to lead an internationally recognized program in hepatobiliary oncology. He is one of Europe's foremost experts on cholangiocarcinoma, with a particular focus on FGFR2 fusion-positive intrahepatic cholangiocarcinoma (iCCA)—a molecular subtype representing approximately 10–15% of iCCA cases that is highly actionable with selective FGFR2 inhibitors. Dr. Vogel served as a key investigator and European leader for the FIGHT-202 trial (pemigatinib) and the PROOF trial (infigratinib), studies that established the first targeted therapies approved specifically for FGFR2-fusion cholangiocarcinoma. Beyond FGFR2, he has contributed to the clinical development of IDH1 inhibitors, HER2-targeted therapies, and immunotherapy combinations in BTC. His translational research program interrogates mechanisms of resistance to FGFR inhibitors, including FGFR2 kinase domain mutations and adaptive FGF ligand upregulation, and explores strategies to overcome or prevent such resistance.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
FIGHT-202 & PROOF Trials — FGFR2 Inhibitors in Cholangiocarcinoma
Served as principal European investigator for pivotal trials of selective FGFR2 inhibitors pemigatinib (FIGHT-202, ORR 35.5%, FDA approved 2020) and infigratinib (PROOF, ORR 23.1%, FDA approved 2021) in previously treated FGFR2 fusion/rearrangement-positive iCCA, establishing FGFR2 targeting as a validated therapeutic strategy.
Mechanisms of Resistance to FGFR2 Inhibitors
Characterized acquired resistance mechanisms to selective FGFR inhibitors in iCCA, identifying secondary FGFR2 kinase domain mutations (gatekeeper V564F, molecular brake N550K/H, activation loop K660M) that inform the development of next-generation non-selective and covalent FGFR inhibitors.
Molecular Profiling and Trial Design for BTC
Contributed to European consensus guidelines and ESMO recommendations for comprehensive molecular profiling of all advanced BTC patients, advocating for routine FGFR2, IDH1, HER2, BRAF, and NTRK testing to enable access to approved targeted therapies and clinical trials.
HCC Preclinical and Translational Research
Conducted extensive preclinical studies on hepatocyte growth factor/MET signaling, FGF19/FGFR4 axis, and Wnt/β-catenin pathway in HCC, identifying oncogenic drivers and potential combination strategies that have informed clinical trial design.
Representative Works 代表性著作
Pemigatinib for previously treated, locally advanced or metastatic cholangiocarcinoma: a multicentre, open-label, phase 2 study (FIGHT-202)
The Lancet Oncology (2020)
Phase II trial demonstrating 35.5% ORR with pemigatinib in FGFR2 fusion-positive cholangiocarcinoma, leading to the first FGFR-targeted FDA approval in biliary tract cancer.
Landscape of somatic mutations in cholangiocarcinoma
Nature Genetics (2012)
Landmark genomic study identifying IDH1/2 mutations, FGFR2 fusions, and other actionable alterations in cholangiocarcinoma, defining the molecular landscape that underpins targeted therapy development.
Acquired resistance to selective FGFR2 inhibitors in patients with cholangiocarcinoma
Cancer Cell (2021)
Analysis of on-treatment biopsies identifying polyclonal FGFR2 kinase domain mutations as the dominant mechanism of acquired resistance to pemigatinib and infigratinib, guiding next-generation FGFR inhibitor development.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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