Richard S. Finn
理查德·芬恩
MD
Professor of Medicine, Division of Hematology/Oncology; Director, Signal Transduction and Therapeutics Program, Jonsson Comprehensive Cancer Center医学教授,血液/肿瘤科,信号转导与治疗学项目主任
👥Biography 个人简介
Richard S. Finn, MD is Professor of Medicine at UCLA's David Geffen School of Medicine and one of the leading clinical investigators reshaping the first-line treatment of hepatocellular carcinoma. He was the global principal investigator for the IMbrave150 trial—the phase III study comparing atezolizumab plus bevacizumab versus sorafenib in previously untreated advanced HCC—which demonstrated significant improvements in both overall survival (HR 0.58) and progression-free survival, leading to the FDA approval of the combination in 2020 and displacing sorafenib as the primary standard of care. Dr. Finn was also a steering committee leader for the HIMALAYA trial, which established the STRIDE regimen (single priming dose of tremelimumab plus durvalumab) as another first-line option in HCC. His research interests span the biology of antiangiogenic and immune synergy in HCC, mechanisms of intrinsic and acquired resistance to immunotherapy in the liver microenvironment, and next-generation combination strategies. He also has major expertise in breast cancer and has led pivotal CDK4/6 inhibitor trials, reflecting his broad signal-transduction oncology focus.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
IMbrave150 Trial — Atezolizumab + Bevacizumab in HCC
Served as global PI for the IMbrave150 phase III trial showing that atezolizumab plus bevacizumab improved OS (HR 0.58) and PFS (HR 0.59) versus sorafenib in untreated advanced HCC, resulting in FDA approval in May 2020 and establishing a new first-line standard based on immune-antiangiogenic synergy.
HIMALAYA Trial — Dual Checkpoint Blockade in HCC
Contributed to the HIMALAYA trial demonstrating that STRIDE (single-dose tremelimumab + regular durvalumab) improved 3-year OS rates versus sorafenib in first-line HCC, providing an anti-CTLA-4/anti-PD-L1 combination option for patients ineligible for bevacizumab.
Biological Rationale for VEGF-Immunotherapy Combinations
Elaborated the mechanistic basis for combining VEGF pathway blockade with PD-L1 inhibition in HCC: bevacizumab normalizes tumor vasculature and mitigates VEGF-mediated immunosuppression, creating a permissive immune microenvironment that enhances atezolizumab efficacy—a paradigm extended to multiple tumor types.
Predictive Biomarker Research for HCC Immunotherapy
Led translational research within IMbrave150 and subsequent studies to identify molecular and immunological biomarkers—including PD-L1 expression, AFP levels, etiology (HBV/HCV/NASH), and tumor mutational burden—predictive of benefit from checkpoint inhibitor combinations in HCC.
Representative Works 代表性著作
Atezolizumab plus Bevacizumab in Unresectable Hepatocellular Carcinoma
New England Journal of Medicine (2020)
IMbrave150 phase III trial demonstrating superior OS and PFS for atezolizumab plus bevacizumab versus sorafenib in advanced HCC, establishing the combination as the new first-line standard.
Tremelimumab plus Durvalumab in Unresectable Hepatocellular Carcinoma (HIMALAYA)
Nature Medicine (2022)
Phase III trial showing improved 3-year OS survival rate (30.7% vs 24.9%) with STRIDE dual checkpoint regimen versus sorafenib in first-line advanced HCC.
Updated efficacy and safety data and impact of hepatitis B virus suppression in IMbrave150
Journal of Hepatology (2022)
Updated IMbrave150 analysis confirming sustained OS benefit (HR 0.66 at updated follow-up) and demonstrating consistent benefit regardless of HBV/HCV status.
🏆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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