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clinical / clinicalhead neck oncology

Tan Eng Huat

陈英发

MBBS, MRCP (UK), FAMS

🏢National Cancer Centre Singapore(新加坡国家癌症中心)🌐Singapore

Senior Consultant, Division of Medical Oncology; Adjunct Professor, Duke-NUS Medical School肿瘤内科高级顾问;杜克-新加坡国立大学医学院兼职教授

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h-index
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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Tan Eng Huat, MBBS, MRCP (UK), FAMS is a Senior Consultant in Medical Oncology at the National Cancer Centre Singapore (NCCS) and Adjunct Professor at Duke-NUS Medical School. He is one of Southeast Asia's leading clinician-scientists in nasopharyngeal carcinoma (NPC), a cancer of major public health significance in the region. Dr. Tan has contributed extensively to defining the role of platinum-based chemotherapy regimens in locoregionally advanced and metastatic NPC, and has led landmark Asian cooperative group trials including studies of gemcitabine-cisplatin chemotherapy and concurrent chemoradiotherapy optimization in this EBV-related malignancy. He has played a critical role in establishing the efficacy of PD-1 checkpoint inhibitors (camrelizumab, nivolumab) in recurrent/metastatic NPC through international and regional phase III trials. Dr. Tan serves on multiple international HNSCC guideline committees and has mentored a generation of Asian NPC investigators.

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🧪Research Fields 研究领域

Nasopharyngeal Carcinoma鼻咽癌
EBV-Associated MalignanciesEBV相关肿瘤
Concurrent Chemoradiotherapy同步放化疗
Immunotherapy NPC鼻咽癌免疫治疗
Head and Neck Cancer Singapore新加坡头颈癌

🎓Key Contributions 主要贡献

Gemcitabine-Cisplatin in Recurrent/Metastatic NPC

Led or co-led the phase III trial demonstrating superiority of gemcitabine plus cisplatin over fluorouracil plus cisplatin as first-line chemotherapy for metastatic or recurrent NPC, establishing a new Asian and international standard of care that remained dominant for over a decade.

PD-1 Blockade in Recurrent/Metastatic NPC

Contributed to phase II and III trials evaluating camrelizumab (SHR-1210), sintilimab, and nivolumab in R/M NPC, providing evidence for immunotherapy benefit in EBV-positive NPC due to high PD-L1 expression and immune-rich tumor microenvironment.

Concurrent Chemoradiotherapy Optimization in NPC

Participated in SEER and Asian cooperative group trials refining cisplatin dosing schedules, induction chemotherapy sequences, and radiotherapy fractionation for locoregionally advanced NPC, improving locoregional control and long-term survival.

Asian Cooperative Oncology Group (ACOG) Leadership

Served in leadership roles in Asian cooperative oncology networks, designing and conducting NPC clinical trials specifically relevant to Asian patient populations and contributing to harmonization of treatment guidelines across Southeast Asia.

Representative Works 代表性著作

[1]

Randomized trial of gemcitabine-cisplatin versus fluorouracil-cisplatin in recurrent or metastatic nasopharyngeal carcinoma

Journal of Clinical Oncology (2005)

Phase III randomized trial demonstrating superiority of gemcitabine-cisplatin in overall response rate and time to progression vs. fluorouracil-cisplatin in recurrent/metastatic NPC.

[2]

Camrelizumab versus placebo in combination with gemcitabine and cisplatin as first-line treatment for recurrent or metastatic nasopharyngeal carcinoma

The Lancet Oncology (2021)

Phase III CAPTAIN-1st trial showing camrelizumab plus chemotherapy significantly improved PFS vs. chemotherapy alone as first-line treatment for R/M NPC.

[3]

Concurrent cetuximab versus cisplatin with radiotherapy in locoregionally advanced nasopharyngeal carcinoma: a phase II study

Annals of Oncology (2015)

Phase II randomized study comparing EGFR inhibitor cetuximab with standard cisplatin concurrent with radiotherapy in locally advanced NPC, informing selection of optimal concurrent agent.

🏆Awards & Recognition 奖项与荣誉

🏆Singapore National Medical Research Council Outstanding Clinician-Scientist Award
🏆FAMS (Fellow, Academy of Medicine Singapore)
🏆National Cancer Centre Singapore Distinguished Clinician Award

📄Data Sources 数据来源

Last updated: 2026-01-15 | All information from publicly available academic sources

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