Date and Location | 5.30 PM – 7.30 PM
Thursday, April 28, 2011
Marriott Ballroom, Lobby Level
Washington Marriott Wardman Park
2660 Woodley Road NW
Washington, DC 20008
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Target Audience | This educational activity is intended for medical oncologists, radiation oncologists, surgical oncologists, and pathologists actively involved in the management of patients with breast cancer. |
Faculty | Harry Bear, MD, PhD (Chair)
Virginia Commonwealth University
Richmond, Virginia, United States
Michael Dixon, MD
Edinburgh Breast Unit
Western General Hospital
Edinburgh, United Kingdom
Sandra Swain, MD
Washington Hospital Center
Washington, DC, United States |
Learning Objectives | Upon completion of this educational activity, participants should be able to:
- Analyze the role of neoadjuvant therapy in endocrine-responsive breast cancer
- Review current neoadjuvant treatment strategies used in endocrine-responsive breast cancer
- Assess the role of gene expression profiles in selecting optimal neoadjuvant therapy for patients with endocrine-responsive breast cancer
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 Agenda |
| 5.30 PM |
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Welcome and introduction
Harry Bear, MD, PhD
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| 5.35 PM |
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Neoadjuvant therapy of breast cancer: What we know and what we don’t
Harry Bear, MD, PhD
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| 5.55 PM |
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Questions and answers |
| 6.00 PM |
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Debate
Which neoadjuvant treatment strategy is most appropriate for endocrine-responsive breast cancer?
Pro Endocrine Therapy: Michael Dixon, MD
Pro Chemotherapy: Sandra Swain, MD |
| 6.40 PM |
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Debate commentary
Harry Bear, MD, PhD
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| 6.50 PM |
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Biologic determinants of systemic therapy in early breast cancer
Sandra Swain, MD
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| 7.10 PM |
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Questions and answers |
| 7.25 PM |
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Conclusions and take-home messages
Harry Bear, MD, PhD
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| 7.30 PM |
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Adjourn |
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 Disclosure of Conflicts of Interest | In accordance with the ACCME Essentials and Standards, everyone involved in planning or presenting this educational activity will be required to disclose any relevant financial relationships with commercial interests in the healthcare industry, and this information will be made available to participants at the start of the activity. In addition, speakers who incorporate information about off-label or investigational use of drugs or devices are required to disclose that information at the beginning of their presentation. |
 Disclosure of Unlabeled Use | This educational activity may contain discussion of published or and/or investigational uses of agents that are not indicated by the US Food and Drug Administration. Sponsors and supporters of this activity do not recommend the use of any agent outside of the labeled indications.
The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of the sponsors and supporters of this activity. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings. |
Americans with Disabilities Act | If you require reasonable accommodations for a disability in order to participate fully in this continuing education activity, please contact Kimberly Friese at +1 678 892 1364 prior to the live event. |
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Accreditation | This initiative has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME). prIME Oncology is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
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Credit Designation | prIME Oncology designates this educational activity for a maximum of 2.0 AMA PRA Category 1 Credits™. Physicians should only claim credit commensurate with the extent of their participation in the activity. |
Organizer | This meeting is a prIME Oncology activity.

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Support | Support for this activity has been provided by Genentech BioOncology and Genomic Health Inc.


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Fee Information | There is no fee to attend this activity or to obtain continuing medical education credit. Preregistration is not required for this event; however space is limited. |
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