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Translational Medicine / 转化医学Cancer Regulation, FDA Oncology

Tatiana M. Prowell

MD

🏢US Food and Drug Administration; Johns Hopkins🌐USA

Medical Officer and Breast Cancer Scientific Lead

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Key Contributions

👥Biography 个人简介

Tatiana Prowell serves as breast cancer scientific lead at FDA and has championed pathologic complete response as a regulatory endpoint enabling accelerated approval in neoadjuvant breast cancer. Her work has shaped the contemporary framework for neoadjuvant trial design. She has advanced inclusive and innovative regulatory pathways.

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🧪Research Fields 研究领域

breast cancer
neoadjuvant trials
FDA review
pathologic complete response
oncology regulation

🎓Key Contributions 主要贡献

Representative Works 代表性著作

📄Data Sources 数据来源

Last updated: 2026-04-01 | All information from publicly available academic sources

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