Lisa Carey
MD, ScM, FASCO
Richardson and Marilyn Jacobs Preyer Distinguished Professor; Chief, Division of Hematology/Oncology, UNC School of Medicine
👥Biography 个人简介
Lisa Carey is a leading expert in triple-negative breast cancer (TNBC) and breast cancer molecular subtypes at UNC Lineberger Comprehensive Cancer Center. Her work has been foundational in characterizing TNBC as a heterogeneous disease with distinct molecular subtypes — including basal-like, mesenchymal, immunomodulatory, and luminal androgen receptor (LAR) subtypes — each with different biology and potentially different therapeutic vulnerabilities. This molecular taxonomy, developed through the Carolina Breast Cancer Study and related genomic investigations, has guided the development of subtype-specific clinical trials. Carey has led multiple neoadjuvant clinical trials in TNBC, recognizing early that neoadjuvant chemotherapy provides a unique opportunity to assess in vivo drug sensitivity and that pathologic complete response strongly predicts long-term outcomes. She has contributed to understanding why some TNBC tumors respond dramatically to neoadjuvant therapy while others do not, and she has advocated for post-neoadjuvant strategies such as capecitabine in residual disease. Her research also encompasses inflammatory breast cancer, a particularly aggressive presentation with unique biology. She has been a leading voice in cooperative group trial design for TNBC and sits on national guideline panels, shaping standards for TNBC treatment. Her commitment to health disparities research — particularly the overrepresentation of Black women among TNBC cases — has been a hallmark of her career.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
TNBC Molecular Subtype Classification
Co-developed and refined classification of TNBC into molecular subtypes (BL1, BL2, M, MSL, IM, LAR) through transcriptomic analyses, establishing a framework for subtype-specific therapeutic targeting that is now widely cited and used in clinical research.
Neoadjuvant Therapy and pCR as a Surrogate Endpoint
Demonstrated through multiple trials and meta-analyses that pathologic complete response after neoadjuvant chemotherapy in TNBC is a strong surrogate for long-term event-free and overall survival, supporting its use as an endpoint for regulatory studies.
Androgen Receptor-Targeted Therapy in LAR-TNBC
Characterized the luminal androgen receptor (LAR) TNBC subtype and led clinical investigations of androgen receptor inhibitors such as enzalutamide and bicalutamide as targeted therapies for this subset of patients.
Health Disparities in Breast Cancer
Led the Carolina Breast Cancer Study investigations showing higher rates of aggressive TNBC in Black women, identifying both biologic and socioeconomic contributors to disparities, and informing targeted outreach and research initiatives.
Representative Works 代表性著作
Molecular Heterogeneity and Response to Neoadjuvant Human Epidermal Growth Factor Receptor 2 Targeting in CALgb 40601
Journal of Clinical Oncology (2016)
Identified molecular subtypes and biomarkers predicting response to HER2-targeted neoadjuvant regimens in HER2+ breast cancer.
TBCRC 001: Randomized Phase II Study of Cetuximab in Combination with Carboplatin in Stage IV Triple-Negative Breast Cancer
Journal of Clinical Oncology (2012)
Early trial demonstrating carboplatin activity in TNBC and the role of EGFR inhibition, informing biomarker studies in TNBC.
Triple-Negative Breast Cancer: Disease Entity or Title of Convenience?
Nature Reviews Clinical Oncology (2010)
Landmark review establishing that TNBC is not a single disease but a collection of molecularly distinct subtypes requiring individualized therapeutic approaches.
🏆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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