Recent Progress in Targeted Therapies and Individualized Treatment Selection for Breast Cancer
Cancer Summaries and Commentaries, Vol. 2, No. 4
1 AMA PRA Category 1 Credit(s)™
Release Date: December 22, 2009
Expiration Date: December 22, 2010
Medical writer: Kristin Garcia, PhD; Medical writer: Timothy Quill, PhD; Reviewed by: Mohammed Jahanzeb, MD, FACP
Recent clinical trial data illustrate the ever-expanding therapeutic options for patients with breast cancer and the increased desire to tailor therapies to particular tumor subtypes. There has been a substantial focus on targeted therapies for the treatment of breast cancer, although proper clinical application of these new therapeutic strategies can be complex. The novel approach of targeting DNA repair pathways through inhibition of poly(ADP) ribose polymerase (PARP) in triple-negative breast cancer has gained attention, with PARP inhibitors demonstrating significant efficacy in this difficult-to-treat tumor subtype. Additionally, investigations are continuing to examine the optimal chemotherapeutic partners for antiangiogenic monoclonal antibodies and tyrosine kinase inhibitors in metastatic breast cancer (MBC), including novel taxane formulations and antimetabolites. In HER2+ breast cancer, the role of focal HER2-amplified clones on HER2 testing and benefit from therapy is currently under investigation. Lastly, HER2-targeted antibody-drug conjugates are demonstrating substantial activity in patients with disease progression on standard HER2-targeted therapy and are increasing the therapeutic options beyond progression. Ultimately, optimizing disease outcome for patients with breast cancer is dependent on physicians staying informed of therapeutic options with careful patient selection, management of toxicities, and enrollment on appropriate clinical trials.
The purpose of this activity is to update physicians on clinically important data regarding the integration of targeted therapies into the treatment of patients with breast cancer and the selection of therapy based on biologic tumor characteristics.
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.
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Complete the test(s) and evaluation by December 22, 2010 to receive your certificate online.
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Mohammed Jahanzeb, MD, FACP
Research Funding – Genentech, Inc., OXiGENE, Inc., Pfizer Inc.; Advisory Board – Abraxis BioScience, LLC; AstraZeneca, Bayer Pharmaceuticals Corporation, Bristol-Myers Squibb Company, Eisai Inc., Eli Lilly and Company, Genentech, Inc., GlaxoSmithKline, ImClone Systems Incorporated, Novartis Pharmaceuticals Corporation, Onyx Pharmaceuticals, Inc., OXiGENE, Inc., Pfizer Inc., sanofi-aventis U.S.; Speaker’s Bureau – Abraxis BioScience, LLC; AstraZeneca, Genentech, Inc., GlaxoSmithKline, Roche Pharmaceuticals, sanofi-aventis U.S.
PER Editorial Staff
No relevant relationships to disclose
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An educational grant for this activity was provided by Genentech BioOncology.
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