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Controversies in Adjuvant Endocrine Therapy for Breast Cancer Summaries of Lectures From a Satellite Symposium Held in Conjunction With the 30th Annual San Antonio Breast Cancer Symposium; San Antonio, TX; December 13-16, 2007 1 AMA PRA Category 1 Credit™ Release date: April 25,
2008 Table of Contents
Optimizing Endocrine Therapy for Patients
With Newly Diagnosed Early-Stage Breast
Cancer Controversies in Adjuvant Endocrine Therapy:
Extending Therapy Beyond 5 Years Should All Patients Receiving Adjuvant
Aromatase Inhibitors for Breast Cancer Receive
Bisphosphonate Support? |
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| Instructions for Participation | ||||
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| Overview and Purpose | ||||
Adjuvant endocrine therapy significantly improves the outcome for patients with hormone receptor–positive early-stage breast cancer, and the recent introduction of aromatase inhibitors (AIs) for postmenopausal patients in this setting has led to further improvements. However, many questions remain concerning the optimal use of these powerful therapeutic tools. Debate continues concerning the optimal treatment strategy: up-front administration of these agents in place of tamoxifen or switching to an AI following 2-3 years of tamoxifen. In addition, the question has been raised whether 5 years of adjuvant endocrine therapy affords maximum benefit to patients or if an extended course of these agents beyond 5 years could further reduce the relative risk of recurrence. These issues must also be considered with regard to the comparative toxicity profiles of the available endocrine therapy regimens and whether supportive therapy measures using bisphosphonates are warranted for all patients receiving AIs to attenuate bone-related adverse events. Despite the significant clinical benefits resulting from the use of adjuvant endocrine therapy for the treatment of hormone receptor–positive breast cancer, further research and careful analyses of existing data are still needed to optimize efficacy while reducing treatment-related side effects for patients in this setting. The purpose of this activity is to apprise physicians of current data on the use of adjuvant endocrine therapy and to highlight key points of controversy regarding their optimal use in treatment regimens for hormone receptor–positive breast cancer. |
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| Target Audience | ||||
| This 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 are required for successful participation in this activity. | ||||
| Learning Objectives | ||||
| Upon completion of this educational activity, you should be able to: | ||||
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| Accreditation and Credit Designation | ||||
| Physicians' Education Resource is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
Physicians' Education Resource designates this educational activity for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity. |
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| Disclosure Policy | ||||
It is the policy of Physicians’ Education Resource to ensure balance, independence, objectivity, and scientific rigor in all of its educational activities. As an organization accredited by the Accreditation Council for Continuing Medical Education (ACCME), Physicians’ Education Resource requires everyone who is in a position to control the content of an educational activity, including spouses/partners, to disclose all relevant financial relationships with any commercial interest. The ACCME defines “relevant financial relationships” as financial relationships in any amount occurring within the past 12 months that create a conflict of interest. Physicians’ Education Resource has implemented a mechanism to identify and resolve all conflicts of interest prior to the activity. PER Editorial Staff No relevant relationships to disclose Satellite Faculty Adam Brufsky, MD, PhD Harold Burstein, MD, PhD Alan Coates, MD, FRACP, Astat, AM Matthew Ellis, MB BChir, PhD, FRCP Julie Gralow, MD James N. Ingle, MD Kathleen Pritchard, MD, FRCP(C) This CME activity might include discussion of investigational and/or unlabeled uses of drugs. If the activity includes discussion of investigational and/or unlabeled uses of a drug, specific information is located on the article page. Please refer to the full prescribing information for each drug discussed in this activity for FDA-approved dosing, indications, and warnings. |
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| Commercial Support | ||||
An educational grant for this activity was provided by Novartis Oncology. |
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| Disclaimer | ||||
| The views and opinions expressed in this activity are those of the authors and do not necessarily reflect the views of the sponsor, supporter, or publisher. Although great care has been taken in compiling and checking the information given in this activity to ensure accuracy, the authors and Physicians’ Education Resource and its servants or agents shall not be responsible or in any way liable for the continued currency of the information or for any errors, omissions, or inaccuracies in this activity, whether arising from negligence or otherwise howsoever or for any consequences arising therefrom. Please consult full prescribing information for any drugs or procedures discussed within. |
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