Geoffrey R. Oxnard
MD
Chief Medical Officer
👥Biography 个人简介
Geoffrey R. Oxnard, MD, is the Chief Medical Officer at Foundation Medicine and a recognized authority on liquid biopsy and circulating tumor DNA (ctDNA) analysis in non-small cell lung cancer. Trained as a thoracic oncologist at Massachusetts General Hospital and Dana-Farber Cancer Institute, his clinical and research career has centered on developing and validating non-invasive genotyping approaches that can guide the selection and monitoring of targeted therapies. His work has been fundamental to establishing plasma genotyping as a clinically viable and increasingly preferred alternative to invasive tumor biopsy in patients with advanced NSCLC. Oxnard's research on plasma-based detection of the EGFR T790M resistance mutation was pivotal in supporting clinical programs for osimertinib, demonstrating that liquid biopsy could reliably identify patients who would benefit from third-generation EGFR inhibitor therapy. He validated the performance characteristics of commercially available cell-free DNA assays and contributed to regulatory deliberations about the role of plasma genotyping in drug approval processes. He also led work on ctDNA dynamics as pharmacodynamic and predictive biomarkers during targeted therapy, establishing frameworks now widely used in clinical trials. Since transitioning to his leadership role at Foundation Medicine, Oxnard has worked to scale genomic profiling for broader clinical adoption and to integrate ctDNA monitoring into routine oncology practice. He has been an active contributor to ASCO, IASLC, and guideline development panels, and remains a frequent author and speaker advancing the scientific and practical dimensions of liquid biopsy in thoracic oncology and beyond.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
Plasma EGFR T790M Detection
Established the clinical validity of plasma-based detection of EGFR T790M mutation, enabling non-invasive identification of patients eligible for osimertinib and informing FDA guidance on the use of liquid biopsy in drug approvals.
Liquid Biopsy Validation in NSCLC
Led rigorous analytical and clinical validation studies of cell-free DNA assays for comprehensive NSCLC genotyping, demonstrating concordance with tissue profiling and establishing performance benchmarks for plasma tests.
ctDNA as Pharmacodynamic Biomarker
Demonstrated that early ctDNA dynamics predict clinical response to targeted therapy in NSCLC, providing a framework for using liquid biopsy as an on-treatment pharmacodynamic readout in clinical trials and practice.
Clinical Adoption of Genomic Profiling
Advanced the field-wide transition toward routine comprehensive genomic profiling in NSCLC through publications, guidelines contributions, and his leadership at Foundation Medicine scaling liquid and tissue-based profiling platforms.
Representative Works 代表性著作
Noninvasive Assessment of Early Tumor Response Using Cell-Free DNA
Science Translational Medicine (2014)
Demonstrated that plasma ctDNA levels correlate with tumor burden and response to therapy in NSCLC, establishing the basis for liquid biopsy as a monitoring tool.
Association Between Plasma Genotyping and Outcomes of Treatment With Osimertinib in Advanced Non–Small-Cell Lung Cancer
Journal of Clinical Oncology (2016)
Validated plasma detection of EGFR T790M as a reliable guide for osimertinib selection and demonstrated clinical outcomes associated with plasma genotyping results.
Analytical Validation of a Cancer Genomic Profiling Assay by Massively Parallel Sequencing
Clinical Cancer Research (2013)
Established rigorous analytical validation standards for next-generation sequencing-based tumor profiling, underpinning the clinical deployment of comprehensive genomic profiling in oncology.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-05 | All information from publicly available academic sources
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