Hossein Borghaei
侯赛因·博尔盖
DO, MS
Chief of Thoracic Medical Oncology; E. Doris Caldwell Endowed Chair in Oncology胸部肿瘤内科主任;E. 多丽丝·考德威尔肿瘤学捐赠讲席教授
👥Biography 个人简介
Hossein Borghaei, DO, MS, is Chief of Thoracic Medical Oncology and holder of the E. Doris Caldwell Endowed Chair in Oncology at Fox Chase Cancer Center. He is the principal investigator of the CheckMate 057 trial that established nivolumab as a second-line therapy for non-squamous NSCLC, the pivotal counterpart to CheckMate 017, and together these two trials underpinned the first FDA approvals for PD-1 inhibition in lung cancer. Borghaei subsequently led the CheckMate 227 trial, a complex multi-part phase III study evaluating nivolumab plus ipilimumab dual checkpoint blockade as first-line therapy for advanced NSCLC. CheckMate 227 demonstrated that nivolumab plus ipilimumab provides superior OS compared to chemotherapy in patients with TMB ≥10 mutations/megabase and in the unselected all-comers population regardless of PD-L1, leading to FDA approval of this doublet immunotherapy combination. His research has also addressed the clinical and translational implications of TMB testing from tissue biopsy and the differential outcomes observed in tobacco-associated versus tobacco-naive NSCLC with immunotherapy. Borghaei is an active contributor to NCCN guidelines for lung cancer and lectures widely on dual checkpoint blockade strategies, immune-related adverse event management, and biomarker-guided immunotherapy selection in thoracic malignancies.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
CheckMate 057: Nivolumab in Non-Squamous NSCLC
Led CheckMate 057 demonstrating nivolumab superiority over docetaxel in previously treated non-squamous NSCLC, providing the pivotal evidence for FDA approval of nivolumab in this setting and complementing CheckMate 017 to establish PD-1 inhibition across NSCLC histologies.
CheckMate 227: Nivolumab plus Ipilimumab First-Line
Principal investigator of CheckMate 227, establishing nivolumab plus ipilimumab dual checkpoint blockade as a chemotherapy-free first-line treatment option for advanced NSCLC across PD-L1 and TMB subgroups, with particularly strong benefit in TMB-high patients.
TMB as Predictive Biomarker for Dual Checkpoint Blockade
Utilized CheckMate 227 platform to prospectively validate tissue TMB ≥10 mut/Mb as a predictive biomarker for nivolumab plus ipilimumab PFS benefit, contributing to the FDA's initial approval of the TMB indication for nivolumab in NSCLC.
Representative Works 代表性著作
Nivolumab versus Docetaxel in Advanced Nonsquamous Non–Small-Cell Lung Cancer (CheckMate 057)
New England Journal of Medicine (2015)
Phase III trial demonstrating OS benefit of nivolumab over docetaxel in previously treated non-squamous NSCLC, with improved responses in PD-L1 expressing tumors, establishing nivolumab as a second-line immunotherapy standard.
Nivolumab plus Ipilimumab in Advanced Non–Small-Cell Lung Cancer (CheckMate 227)
New England Journal of Medicine (2019)
Phase III trial showing superior OS with nivolumab plus ipilimumab versus chemotherapy as first-line therapy for advanced NSCLC regardless of PD-L1 expression, with enhanced benefit in TMB-high patients, establishing a chemotherapy-free dual checkpoint option.
Nivolumab plus Ipilimumab versus Chemotherapy as First-Line Treatment: 4-Year Outcomes (CheckMate 227)
Journal of Clinical Oncology (2021)
Long-term 4-year follow-up demonstrating sustained OS benefit with nivolumab plus ipilimumab over chemotherapy with a 4-year OS rate of 29% versus 18%, reinforcing dual checkpoint blockade as a durable first-line option.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-01-15 | All information from publicly available academic sources
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