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Translational Medicine / 转化医学Breast Cancer & HER2

Sara Hurvitz

MD, FACP

🏢UC San Diego Moores Cancer Center🌐USA

Director, Breast Oncology Program; Professor of Medicine, UC San Diego

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Sara Hurvitz is Director of the Breast Oncology Program at UC San Diego Moores Cancer Center and one of the world's leading experts on HER2-directed antibody-drug conjugates. She has played a central role in the clinical development of trastuzumab deruxtecan (T-DXd, Enhertu), serving as a principal investigator on the pivotal DESTINY-Breast series of trials. Her work has redefined the treatment paradigm not only for HER2-positive breast cancer but, crucially, for the newly defined HER2-low category, a patient population previously lacking HER2-directed options. Hurvitz was the lead investigator for DESTINY-Breast03, the landmark head-to-head trial comparing T-DXd to ado-trastuzumab emtansine (T-DM1) in previously treated HER2+ metastatic breast cancer, which demonstrated dramatically superior outcomes for T-DXd and led to its FDA approval as a second-line standard of care. She has also led early-phase studies exploring T-DXd in new combinations and lines of therapy, as well as investigations into biomarkers predicting response. Beyond T-DXd, Hurvitz has contributed to the clinical evaluation of bispecific antibodies, tyrosine kinase inhibitors, and immune checkpoint combinations in HER2+ breast cancer. She is committed to integrating biomarker science into clinical trial design and to training the next generation of breast oncology researchers.

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🧪Research Fields 研究领域

Trastuzumab deruxtecan (T-DXd)
HER2-low breast cancer
DESTINY-Breast trials
Antibody-drug conjugates
HER2+ metastatic breast cancer

🎓Key Contributions 主要贡献

DESTINY-Breast Clinical Trial Series

Served as global principal investigator for DESTINY-Breast03, demonstrating T-DXd superiority over T-DM1 in HER2+ metastatic breast cancer with unprecedented PFS and response rates, establishing T-DXd as the new second-line standard of care.

HER2-Low Breast Cancer Definition and Treatment

Co-led DESTINY-Breast04 demonstrating T-DXd efficacy in HER2-low breast cancer (IHC 1+ or 2+/ISH-), establishing a new targetable patient population and reshaping how HER2 expression is classified and treated.

Antibody-Drug Conjugate Clinical Development

Contributed to the broader clinical development of ADCs in breast cancer, including investigation of optimal sequencing, combination strategies, and management of ADC-associated toxicities including interstitial lung disease.

Biomarker Science for HER2-Directed Therapy

Investigated predictive biomarkers for T-DXd response and resistance, including HER2 expression levels, tumor heterogeneity, and molecular subtypes, to refine patient selection strategies.

Representative Works 代表性著作

[1]

Trastuzumab Deruxtecan versus Trastuzumab Emtansine for Breast Cancer (DESTINY-Breast03)

New England Journal of Medicine (2022)

Demonstrated overwhelming superiority of T-DXd over T-DM1 in previously treated HER2+ metastatic breast cancer, with 12-month PFS of 75.8% vs 34.1%.

[2]

Trastuzumab Deruxtecan in Previously Treated HER2-Low Advanced Breast Cancer (DESTINY-Breast04)

New England Journal of Medicine (2022)

Established T-DXd as the first HER2-directed therapy to show significant benefit in HER2-low breast cancer, transforming treatment for this large patient population.

[3]

Trastuzumab Deruxtecan (DS-8201a) in HER2-Positive Metastatic Breast Cancer: Results of a Phase 1 Study

Journal of Clinical Oncology (2020)

First-in-human dose escalation and expansion study demonstrating remarkable activity of T-DXd in heavily pretreated HER2+ breast cancer.

🏆Awards & Recognition 奖项与荣誉

🏆ASCO Young Investigator Award
🏆SABCS Outstanding Investigator Award
🏆Conquer Cancer Foundation Career Development Award

📄Data Sources 数据来源

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

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