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Translational Medicine / 转化医学melanoma oncology

Mark R. Middleton

马克·米德尔顿

PhD, FRCP

🏢University of Oxford / Churchill Hospital(牛津大学 / 丘吉尔医院)🌐UK

Professor of Experimental Cancer Medicine; Head, Oncology Department实验肿瘤医学教授;肿瘤科主任

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Mark Middleton, PhD, FRCP is Professor of Experimental Cancer Medicine at the University of Oxford and a key investigator in the development of tebentafusp, the first therapy to demonstrate overall survival benefit in metastatic uveal melanoma. His research program encompasses rare melanoma subtypes including uveal, acral, and mucosal melanoma, diseases with distinct biology and historically limited treatment options that differ fundamentally from cutaneous UV-driven melanoma.

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🧪Research Fields 研究领域

Uveal Melanoma葡萄膜黑色素瘤
Tebentafusp替苯他福
GNAQ GNA11 MutationsGNAQ/GNA11突变
Acral Melanoma肢端黑色素瘤
Mucosal Melanoma黏膜黑色素瘤
Melanoma Clinical Trials黑色素瘤临床试验

🎓Key Contributions 主要贡献

Tebentafusp in Metastatic Uveal Melanoma

Key investigator on the IMCgp100-202 phase III trial of tebentafusp (a gp100xCD3 ImmTAC bispecific) versus investigator's choice, demonstrating the first overall survival benefit in metastatic uveal melanoma and supporting approval in HLA-A*02:01-positive patients.

Biology of Non-UV Melanoma Subtypes

Conducted translational studies characterizing the genomic and immunological landscape of acral and mucosal melanoma, informing rational treatment strategies for these UV-signature-negative subtypes with distinct driver mutations.

Early Phase Oncology Program at Oxford

Built and leads the Oxford experimental cancer medicine center, conducting first-in-human and early-phase trials of novel immunological agents across melanoma and solid tumors.

Representative Works 代表性著作

[1]

Tebentafusp versus investigator's choice in metastatic uveal melanoma (IMCgp100-202)

New England Journal of Medicine (2021)

Phase III trial demonstrating significantly improved overall survival with tebentafusp in HLA-A*02:01-positive metastatic uveal melanoma, the first survival benefit ever shown in this disease.

[2]

Genomic analysis of acral and mucosal melanoma

Cancer Research (2019)

Comprehensive genomic characterization of non-UV melanoma subtypes revealing distinct mutational spectra including KIT, NRAS, and CDK4 alterations relevant to therapeutic targeting.

🏆Awards & Recognition 奖项与荣誉

🏆Cancer Research UK Outstanding Achievement Award
🏆British Association of Dermatologists Research Prize
🏆ESMO Young Oncologist Award

📄Data Sources 数据来源

Last updated: 2026-01-20 | All information from publicly available academic sources

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