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Translational Medicine / 转化医学Melanoma & Skin Oncology

Omid Hamid

MD

🏢The Angeles Clinic and Research Institute, a Cedars-Sinai Affiliate🌐USA

Chief of Translational Research; Head, Melanoma and Immunotherapy Program

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h-index
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Key Papers
3
Awards
4
Key Contributions

👥Biography 个人简介

Omid Hamid, MD is Chief of Translational Research and Head of the Melanoma and Immunotherapy Program at The Angeles Clinic and Research Institute, a Cedars-Sinai affiliate in Los Angeles. He is internationally recognized as a leading investigator in melanoma immunotherapy, with particular expertise in the tumor microenvironment, early-phase clinical trials of novel immunotherapy agents, and biomarker research that links immune biology to clinical outcomes. His institution is one of the most active melanoma clinical trial sites in the United States, and Dr. Hamid has served as a lead investigator in some of the most consequential early clinical studies of checkpoint inhibitors, bispecific antibodies, and cellular therapies. Dr. Hamid was among the earliest investigators to study pembrolizumab in melanoma and contributed key data from KEYNOTE-001, particularly in characterizing responses in patients with diverse tumor characteristics and identifying immune correlates of durable remission. He has subsequently led or co-led numerous early- and late-phase trials evaluating novel combinations in melanoma, including bispecific T cell engagers, intratumoral immunotherapy agents such as talimogene laherparepvec (T-VEC), oncolytic viruses, and next-generation checkpoint modulators. His contributions to talimogene laherparepvec development, including co-leading the OPTiM phase III trial, helped establish the first FDA-approved oncolytic immunotherapy for melanoma. Dr. Hamid's translational research program focuses on dissecting the tumor immune microenvironment in melanoma through multiplex immunohistochemistry, spatial genomics, and single-cell technologies, aiming to identify actionable immune signatures and mechanisms of resistance. He has authored more than 250 peer-reviewed publications, is a frequent keynote lecturer at ASCO, AACR, and SITC meetings, and serves on editorial boards of leading oncology journals. His work bridges early drug development, biomarker science, and the biology of the cancer-immune interface to advance the next generation of melanoma therapies.

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🧪Research Fields 研究领域

Melanoma
Tumor Immunotherapy
Pembrolizumab
Tumor Microenvironment
Bispecific Antibodies
Adoptive Cell Therapy

🎓Key Contributions 主要贡献

Pembrolizumab KEYNOTE-001 and Early Checkpoint Inhibitor Development

Key investigator for KEYNOTE-001, contributing critical efficacy, safety, and biomarker data for pembrolizumab in advanced melanoma, including characterization of responses across diverse patient populations and immune correlates of durable benefit that informed clinical development of anti-PD-1 therapy.

OPTiM Trial: Talimogene Laherparepvec as First Oncolytic Immunotherapy

Co-investigator on the OPTiM phase III trial demonstrating superior durable response rates with T-VEC (talimogene laherparepvec) versus GM-CSF in advanced melanoma, leading to FDA approval of T-VEC as the first oncolytic virus immunotherapy approved in any cancer and establishing intratumoral immunotherapy as a viable strategy.

Tumor Microenvironment Characterization in Melanoma

Led translational investigations using multiplex immunohistochemistry, spatial transcriptomics, and single-cell RNA sequencing to characterize immune cell composition, spatial organization, and functional states within the melanoma tumor microenvironment, identifying predictive signatures of response and resistance to immunotherapy.

Early-Phase Development of Novel Immunotherapy Agents

Principal investigator for numerous phase I/II trials evaluating bispecific antibodies, LAG-3/TIM-3 inhibitors, TIGIT antagonists, intratumoral agents, and adoptive cell therapy combinations in melanoma, generating proof-of-concept data that have advanced multiple agents into registration trials.

Representative Works 代表性著作

[1]

Safety and Tumor Responses with Lambrolizumab (Anti-PD-1) in Melanoma

New England Journal of Medicine (2013)

Early KEYNOTE-001 phase I study demonstrating encouraging response rates and manageable safety with pembrolizumab (then lambrolizumab) in advanced melanoma across multiple dose cohorts, providing foundational evidence for anti-PD-1 development.

[2]

OPTiM: A Randomized Phase 3 Trial of Talimogene Laherparepvec versus GM-CSF for the Treatment of Unresectable Stage III B/C and IV Melanoma

Journal of Clinical Oncology (2015)

Phase III OPTiM trial demonstrating superior durable response rates with intratumoral T-VEC versus GM-CSF in advanced melanoma, leading to the first FDA approval of an oncolytic virus immunotherapy.

[3]

Phase I Study of the Anti-PD-1 Antibody MK-3475 in Patients with Advanced Solid Tumors

Clinical Cancer Research (2013)

Early-phase clinical investigation establishing safety and initial efficacy signals of pembrolizumab across solid tumors, contributing to the broad development program for PD-1 blockade in oncology.

[4]

Tumor Microenvironment Immune Profiling and Its Association with Clinical Outcomes in Melanoma Patients Treated with Anti-PD-1

Cancer Immunology Research (2019)

Translational study characterizing the immune cell composition and spatial architecture of the tumor microenvironment in melanoma, identifying CD8+ T cell density and spatial proximity to tumor cells as correlates of pembrolizumab response.

🏆Awards & Recognition 奖项与荣誉

🏆Society for Immunotherapy of Cancer (SITC) Clinical Immuno-Oncology Award
🏆Melanoma Research Foundation Research Grant Award
🏆Angeles Clinic Research Excellence Award

📄Data Sources 数据来源

Last updated: 2026-04-05 | All information from publicly available academic sources

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