The Next Generation of Combinations for Breast Cancer: Building on Targeted Therapies
Online Only Cancer Summaries & Commentaries
Release Date: August 22, 2008
Expiration Date: August 22, 2009
PER Editorial Staff
Audio Commentaries by: Joyce O’Shaughnessy, MD
The treatment of breast cancer has evolved rapidly in recent years, primarily due to targeted therapies designed to inhibit pathologic signaling. In particular, endocrine therapy and HER2-targeted agents have significantly improved clinical outcomes in a variety of settings. De novo and acquired resistance to these approaches, however, remain a substantial clinical problem. Methods under investigation to treat HER2+ disease that has progressed on standard antibody-based therapies include the use of small-molecule tyrosine kinase inhibitors (TKIs) targeting HER2 receptor alone or in combination with other HER2-targeted agents, the use of novel antibody-drug conjugates, and the targeting of downstream pathway components. Inhibitors of proteins that drive adaptive responses involved in hormone therapy resistance are also being evaluated. These agents can potentially restore the sensitivity of hormone receptor–positive breast cancers and prevent the emergence of resistance if used earlier in disease progression. The adaptive nature of breast cancer requires the continued development of novel strategies and careful analysis of data from clinical trials investigating methods for overcoming resistance to existing therapies.
The purpose of this activity is to educate physicians on novel strategies designed to prevent or overcome resistance to HER2-targeted agents or endocrine therapy in the treatment of breast cancer.
This educational activity is intended for medical oncologists involved in the care of patients with breast cancer. No specific skills or knowledge other than a basic training in oncology is required for successful participation in this activity.
Upon completion of this educational activity, you should be able to: