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Translational Medicine / 转化医学Breast Cancer & HER2

José Baselga

MD, PhD

🏢Memorial Sloan Kettering Cancer Center / AstraZeneca🌐USA

Former Physician-in-Chief, MSKCC; Former EVP, AstraZeneca Oncology R&D

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

José Baselga was one of the world's foremost authorities on HER2-positive breast cancer and the development of HER2-targeted therapies. As Chief of Hematology/Oncology and later Physician-in-Chief at Memorial Sloan Kettering Cancer Center, he led translational research efforts that fundamentally changed how HER2+ breast cancer is treated. His work on pertuzumab, a second anti-HER2 monoclonal antibody, contributed directly to the landmark CLEOPATRA trial, which demonstrated improved overall survival in metastatic HER2+ breast cancer with the combination of pertuzumab, trastuzumab, and docetaxel. Beyond HER2-targeted therapy, Baselga made major contributions to understanding PI3K pathway alterations in breast cancer and their role in resistance to endocrine and HER2-directed therapies. He led and co-led multiple pivotal clinical trials that informed regulatory approvals of pertuzumab and subsequently influenced neoadjuvant treatment strategies. His translational work bridging genomic insights with clinical applications became a model for precision oncology in breast cancer. Baselga later joined AstraZeneca as Executive Vice President for Oncology R&D, where he guided the development pipeline including antibody-drug conjugates and next-generation targeted agents. He passed away in 2021, leaving behind a scientific legacy that continues to shape breast cancer treatment worldwide.

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🧪Research Fields 研究领域

HER2-targeted therapy
Pertuzumab
PI3K pathway inhibition
Breast cancer clinical trials
Trastuzumab resistance

🎓Key Contributions 主要贡献

Dual HER2 Blockade with Pertuzumab

Co-developed the clinical rationale for combining pertuzumab with trastuzumab, demonstrating that dual HER2 blockade prevents receptor dimerization and overcomes resistance. The CLEOPATRA trial he supported led to FDA approval of pertuzumab for HER2+ metastatic breast cancer.

PI3K/AKT Pathway in Breast Cancer Resistance

Characterized PI3K pathway hyperactivation as a primary driver of resistance to trastuzumab, establishing the scientific foundation for combining PI3K inhibitors with HER2-directed therapy. This work informed multiple subsequent trials of alpelisib and other PI3Ki agents.

Neoadjuvant HER2+ Breast Cancer Trials

Led the NeoSphere trial establishing pertuzumab plus trastuzumab plus docetaxel as a neoadjuvant regimen for HER2+ breast cancer, demonstrating pathologic complete response as a surrogate endpoint for regulatory approval.

Biomarker-Driven Precision Oncology

Championed genomic profiling of breast tumors to identify predictive biomarkers and match patients to targeted therapies, contributing to the broader framework of precision oncology now standard in breast cancer care.

Representative Works 代表性著作

[1]

Pertuzumab plus Trastuzumab plus Docetaxel for Metastatic Breast Cancer (CLEOPATRA)

New England Journal of Medicine (2012)

Pivotal phase III trial showing dual HER2 blockade significantly improved progression-free and overall survival in metastatic HER2+ breast cancer.

[2]

Pertuzumab plus Trastuzumab plus Docetaxel as Neoadjuvant Treatment of HER2-Positive Breast Cancer (NeoSphere)

The Lancet Oncology (2012)

Demonstrated that adding pertuzumab to trastuzumab and docetaxel significantly improved pathologic complete response rates in the neoadjuvant setting.

[3]

Phase I Clinical Trials Using Escalation with Overdose Control

Journal of Clinical Oncology (2006)

Methodological contribution to dose-finding design in early-phase oncology trials, widely cited in breast cancer and other tumor type studies.

🏆Awards & Recognition 奖项与荣誉

🏆ASCO Gianni Bonadonna Breast Cancer Award
🏆American Association for Cancer Research Award
🏆Susan G. Komen Foundation Brinker Award for Scientific Distinction

📄Data Sources 数据来源

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

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