The Breast Cancer Initiative: Addressing Chemotherapy Resistance

A CME/CE Web-Based Activity
April 2008 through June 30, 2009

 

Prior to participating in this activity, please review the information on this page.

Estimated time to complete each module: 60 minutes

 

PROGRAM OVERVIEW

Guidelines and strategies for treating patients with metastatic breast cancer (mBC) are continually changing due to advancements in clinical knowledge and ongoing research. At present, the most active drugs are the anthracyclines and the taxanes. However, responses are often short-lived, and disease progression is almost inevitable. Tumor resistance to cytotoxic agents is commonly observed and occurs through various mechanisms, including biological resistance at the cellular level (eg, altered membrane transport involving product of the multidrug resistance [MDR] gene).

Most recently, epothilones have entered the clinical arena for treating taxane- and anthracycline-refractory metastatic disease.  This new class of agents differs from taxanes in their interaction with microtubules and mechanisms of cellular resistance. In this CME/CE activity, The Breast Cancer Initiative: Addressing Chemotherapy Resistance, each of the 3 modules will familiarize participants with current efficacy and safety data for emerging therapies that overcome resistance, and will help define the optimal position for these therapies within the spectrum of treatment options.

 

TARGET AUDIENCE

The target audience for this activity includes medical and practicing oncologists, oncology nurses, and nurse practitioners who work with patients with metastatic breast cancer.

 

Chair

Sandra M. Swain, MD
Medical Director

Washington Cancer Institute

Washington Hospital Center

Washington, DC

Faculty

Una Hopkins, NP

Nurse Practitioner

Medical Oncology

Albert Einstein Cancer Center

Montefiore Medical Center

Bronx, New York

Faculty

Linda T. Vahdat, MD

Associate Professor, Clinical Medicine

Director, Breast Cancer Center Research Program

Weill Cornell Medical College

Associate Attending

New York Presbyterian Hospital

New York, New York

Mechanisms for
Overcoming
Anthracycline and
Taxane Resistance
 

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Module 1

April 2008

 

After Anthracyclines
and Taxanes:

Emerging Agents and
Clinical Data
 

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Module 2

May 2008

 

Overcoming
Anthracyclines and
Taxane Resistance:
Managing Toxicities

 

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Module 3

June 2008

 

Sponsored by

 Supported by an educational grant from

 

LEARNING OBJECTIVES

Module 1: Mechanisms for Overcoming Anthracycline and Taxane Resistance

  1. You will be able to describe the biologic processes that result in resistance to taxanes and anthracyclines and explain how new agents for metastatic breast cancer (mBC) circumvent these processes to overcome resistance.

  2. You will be able to formulate new treatment strategies for your patients with mBC based on novel epothilone agents.

Module 2: After Anthracyclines and Taxanes: Emerging Agents and Clinical Data

  1. You will be able to evaluate the clinical data emerging from trials using epothilones in the treatment of advanced metastatic breast cancer (mBC) and consider the place for epothilones in your treatment armamentarium.

  2. You will be able to formulate new treatment strategies for your patients with mBC based on novel epothilone agents.

Module3: Overcoming Anthracycline and Taxane Resistance: Managing Toxicities

  1. You will be able to compare the safety profiles of salvage combination therapies for metastatic breast cancer in order to communicate to patients their treatment options after receiving a taxane or anthracycline.
  2. You will be able to formulate new treatment strategies for your patients with metastatic breast cancer based on novel epothilone agents.

 

METHOD OF PARTICIPATION
In order to receive credit for this activity, participants must:

  • View/complete entire module.

  • Complete and submit the CME/CE Activity Evaluation and Request for Credit Form.
  • Print your CME certificate or nursing statement of credit.

 

This activity is provided free of charge to participants.

 

ACCREDITATION/DESIGNATION OF CREDIT STATEMENT

Veritas Institute for Medical Education, Inc. is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education to physicians.

 

Physicians: Veritas Institute for Medical Education, Inc. designates each educational activity for a maximum of 1.0 AMA PRA Category 1 Credit(s)TM.  Physicians should only claim credit commensurate with the extent of their participation in the activity.

 

Nurses: Veritas Institute for Medical Education, Inc. approved by the California Board of Registered Nursing, Provider #13986, for 1 Contact Hour.

Nurse Practitioners: Veritas Institute for Medical Education, Inc. approved as a provider for nurse practitioner continuing education by the American Academy of Nurse Practitioners: AANP Provider number 040309. Each program has been approved for 1.0 contact hour(s) of continuing education (which includes 1.0 hour(s) of pharmacology).

FINANCIAL DISCLOSURE

In accordance with the ACCME’s Standards for Commercial Support, all CME/CE providers are required to disclose to the activity audience the relevant financial relationships of the planners, teachers, and authors involved in the development of CME/CE content. An individual has a relevant financial relationship if he or she has a financial relationship in any amount occurring in the last 12 months with a commercial interest whose products or services are discussed in the CME/CE activity content over which the individual has control. Disclosures are as follows:

Sandra M. Swain, MD: Genentech, Inc. (consultant), Roche Pharmaceuticals, sanofi-aventis (speakers bureau)

Una Hopkins, NP: Bristol-Myers Squibb Company, Genentech, Inc. (consultant), Genomic Health, Inc., MGI PHARMA, INC., Pfizer Inc (speakers bureau), sanofi-aventis (speakers bureau, consultant)

Linda T. Vahdat, MD: Bayer HealthCare Pharmaceuticals, Bristol-Myers Squibb Company, Eisai Inc., Pfizer Inc (grant/research support)

The independent content reviewer, Electa Stern, PharmD: Ortho McNeil, Astelas, sanofi-aventis (advisory board)

The staff of Veritas Institute for Medical Education, Inc. has nothing to disclose.

 

OFF-LABEL/INVESTIGATIONAL USES OF DRUGS/MEDICAL DEVICES DISCLOSURE

Participants are advised that this CME/CE activity will contain references to unlabeled/unapproved/investigational uses of drugs to treat patients with breast cancer.

 

DISCLAIMER

The opinions expressed in this activity are those of the presenters and do not necessarily reflect those of Veritas Institute for Medical Education, Inc., or Bristol-Myers Squibb Company. Please consult the appropriate package insert for full prescribing information on all drug therapies discussed.

 

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