Elizabeth R. Plimack
伊丽莎白·普利马克
MD, MS
Chief, Division of Genitourinary Medical Oncology; Professor of Hematology/Oncology, Fox Chase Cancer Center泌尿生殖医学肿瘤科主任,福克斯蔡斯癌症中心血液/肿瘤学教授
👥Biography 个人简介
Elizabeth R. Plimack, MD, MS is Chief of the Division of Genitourinary Medical Oncology and Professor of Hematology/Oncology at Fox Chase Cancer Center, Temple University Health System. She is a nationally recognized leader in bladder cancer clinical trials and translational research, known for her expertise in biomarker-driven therapy and her pivotal role in practice-changing trials that have reshaped the treatment of advanced urothelial carcinoma. Dr. Plimack was a co-principal investigator for the EV-302 trial (also called KEYNOTE-EV), the landmark phase III study demonstrating that enfortumab vedotin combined with pembrolizumab significantly improved overall survival and progression-free survival compared to platinum-based chemotherapy in previously untreated advanced urothelial carcinoma, establishing a chemotherapy-free first-line standard. Her translational research program at Fox Chase is particularly recognized for discoveries related to DNA damage response (DDR) alterations in bladder cancer. She identified ERCC2 somatic mutations as predictive biomarkers of complete pathological response to cisplatin-based neoadjuvant chemotherapy in muscle-invasive bladder cancer, a finding with major implications for precision perioperative therapy. Dr. Plimack has been a co-investigator on multiple KEYNOTE bladder cancer trials, leads the genitourinary oncology clinical trials portfolio at Fox Chase, and serves on ASCO, NCCN, and SWOG committee panels for bladder and kidney cancer.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
EV-302/KEYNOTE-EV — Enfortumab Vedotin + Pembrolizumab as First-Line Standard in Advanced Urothelial Carcinoma
Served as co-principal investigator for EV-302 (KEYNOTE-EV), which demonstrated that enfortumab vedotin plus pembrolizumab improved overall survival and progression-free survival over platinum-based chemotherapy as first-line treatment for advanced urothelial carcinoma regardless of PD-L1 status or cisplatin eligibility, earning FDA approval and establishing the combination as the new first-line standard of care.
ERCC2 Mutations as Predictors of Cisplatin Response in Muscle-Invasive Bladder Cancer
Conducted landmark discovery and validation analyses demonstrating that somatic ERCC2 mutations — encoding a DNA nucleotide excision repair helicase — predict pathological complete response to cisplatin-based neoadjuvant chemotherapy in muscle-invasive bladder cancer, identifying the first genomic biomarker for cisplatin sensitivity in this disease and laying the foundation for biomarker-stratified perioperative trial design.
DNA Damage Response Alterations and Bladder Cancer Precision Therapy
Expanded the discovery of ERCC2 to a broader DDR alteration signature in bladder cancer, demonstrating that co-occurring mutations in ERCC2, FANCC, and other DNA repair genes correlate with cisplatin sensitivity, informing the biological rationale for PARP inhibitor combinations and DDR-targeted approaches currently under clinical evaluation in urothelial carcinoma.
Perioperative Immunotherapy Trials in Muscle-Invasive Bladder Cancer
Led and co-led multiple phase II and III trials evaluating pembrolizumab-based neoadjuvant and adjuvant immunotherapy strategies in muscle-invasive bladder cancer, probing the interaction of cisplatin with checkpoint inhibition and evaluating ctDNA and genomic correlates of pathological response as surrogate endpoints.
Representative Works 代表性著作
Enfortumab vedotin plus pembrolizumab versus chemotherapy in untreated advanced urothelial cancer (EV-302/KEYNOTE-EV)
New England Journal of Medicine (2024)
Phase III EV-302 trial establishing enfortumab vedotin plus pembrolizumab as superior first-line therapy over platinum-based chemotherapy across all advanced urothelial carcinoma subgroups.
ERCC2 mutations predict response to cisplatin-based chemotherapy in bladder cancer
Nature Genetics (2016)
Discovery paper identifying somatic ERCC2 mutations as the first genomic predictive biomarker for cisplatin sensitivity in muscle-invasive bladder cancer.
Pembrolizumab as neoadjuvant therapy before radical cystectomy in patients with muscle-invasive bladder cancer (PURE-01)
Journal of Clinical Oncology (2019)
Phase II neoadjuvant pembrolizumab trial in muscle-invasive bladder cancer demonstrating pathological complete response correlated with PD-L1 expression and tumor mutational burden.
Mutational landscape of aggressive, early-onset bladder cancer and implications for routine clinical genomic analysis
Cancer Cell (2014)
Comprehensive genomic analysis of aggressive bladder cancer characterizing the mutational landscape and DNA repair gene alterations with implications for biomarker-driven therapy selection.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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