Program Title:  Case Study in Refractory Anemia

Release Date: 2/1/07

Valid Through: 1/31/08

Target Audience:This CME activity is designed for oncologists, hematologists and other healthcare professionals who treat refractoryt anemia.

Learning Objectives

After completing this educational activity, participants should be better able to:

• Understand trilineage response rates among patients with MDS who are treated with azacitidine.
• Evaluate response data from the phase III clinical trial comparing azacitidine to best supportive care in the treatment of MDS.
• Discuss side effects associated with treatment with lenalidomide.
• Understand the role of allogeneic stem cell transplantation among patients with low or intermediate-1 risk MDS.
• Identify the clinical impact of adjuvant chemotherapy on early stage breast cancer patients with a low, intermediate, or high risk for recurrence.
  

Accreditation Statement

This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of Creative Educational Concepts, Inc. (CEC) and OncoEd, Inc. CEC is accredited by the ACCME to provide continuing medical education for physicians.

CEC designates this educational activity for a maximum of 0.5 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

CEC is an equal opportunity/affirmative action institution.

Fee: There is no fee for this activity.

Instructions for Participation

This activity was released February 1, 2007, and will be valid through January 31, 2008. There are no fees for participating and receiving credit for this activity. To successfully complete this activity, participants must do the following:

• Read the target audience, learning objectives, and author disclosures.
• Study the educational activity online or printed out.
• Read, complete, and submit answers to the post test questions and evaluation questions online and click "submit" when finished.
• After clicking "submit," your online certificate will be made available for you to view and print.

Hardware/Software Requirements

This Website requires version 4.x browsers or higher from Microsoft or Netscape. It has been optimized for Microsoft Browsers.

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Faculty and Disclosures

CEC is committed to the provision of CME that is balanced, objective, and evidence based. CEC adheres to Accreditation Council for Continuing Medical Education (ACCME) Essentials and Standards. Accordingly, all parties involved in content development have disclosed any real or apparent conflicts of interest relating to the topics of this educational activity and the disclosure summary follows. CEC has established mechanisms to resolve conflicts of interest should they arise. Participants in CEC CME programs are afforded the opportunity to provide feedback on the quality of individual programs.

Authors: Ravi Vij, MD
Disclosure: Dr. Vij is on the speaker's bureau for Pharmion and Celgene and has received grant/research support from Pharmion and Celgene.

Editor: Adam C. Tanous, Director and Managing Editor, OncoEd, Inc.
Disclosure: Mr. Tanous has no relevant financial interests to disclose.

Disclaimer

Notwithstanding any language to the contrary, nothing contained herein constitutes, nor is intended to constitute, an offer, inducement, promise, or contract of any kind. The data contained herein are for informational purposes only and are not represented to be error free. Any links to non-CEC information are provided as a courtesy. They are not intended to constitute, nor do they constitute, an endorsement of the linked materials by CEC.

Investigational and/or off-label use of commercial products and devices

CEC requires all faculty to disclose any planned discussion of an investigational and/or off-label use of a pharmaceutical product or device within their presentation. Participants should note that the use of products outside FDA-approved labeling should be considered experimental and are advised to consult current prescribing information for approved indications.

The presentations in this CME activity might include discussion of investigational and/or unlabeled use of drugs. Please refer to the full prescribing information for each drug discussed in this activity for FDA-approved dosing, indications, and warnings.

Supporters

This activity is supported by an unrestricted educational grant from Pharmion.