Managing Patients With Breast Cancer Receiving Targeted Therapies

This program was originally presented as an educational symposium during the ONS 8th Annual Institutes of Learning.

Thursday, November 8, 2007
7:30 pm – 9:30 pm (CST)

Regency Ballroom B
Hyatt Regency Chicago
Chicago, Illinois

Release Date: March 2008
Expiration Date:
March 2009
Estimated Time to Complete Activity: 1 hour 57 minutes
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Accreditation Information


Target Audience

This activity has been designed to meet the educational needs of patient care oncology nurses.

Purpose

To review the current and future roles of targeted therapies in the treatment of breast cancer.

Program Overview

In this educational symposium, a breast cancer oncologist will present an overview of the current role of targeted therapies used in the treatment of breast cancer and provide an update on emerging clinical trial data expected to markedly influence practice patterns. The focus will be on issues that affect nurses most, such as agents they can expect to administer, and dosing and scheduling modifications based on new data. The latter half of the program will consist of an interactive workshop in which an expert panel of breast cancer oncology nurses will present and discuss model algorithms for assessing and managing common toxicities specific to breast cancer targeted therapies. An interactive question-and-answer activity will lead participants through common toxicity management algorithms and will help to identify barriers (i.e., institutional, personal, cultural) to algorithm implementation. Strategies for overcoming these barriers will be identified and discussed, ultimately providing attendees with a working model for incorporating upto- date standards into their routine nursing practices. Program attendees will receive several side-effect assessment and management clinical tools, as well as sample patient education tools, to utilize in their individual clinical practices.

Learning Objectives

Upon completion of this program, participants should be better able to:

  • Cite the current paradigm for targeted therapies in the treatment of breast cancer
  • Identify new targeted agents under investigation for the treatment of breast cancer
  • Identify common treatment-related side effects associated with relevant targeted therapies
  • Apply toxicity assessment algorithms for patients receiving HER2 inhibitors and antiangiogenic therapy
  • Describe management strategies for selected toxicities caused by HER2 inhibitors and antiangiogenic therapy
  • Describe strategies for encouraging oral therapy adherence

Disclosure of Unlabeled Use

This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the U.S. Food and Drug Administration. IMER and Genentech BioOncology 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 IMER and Genentech BioOncology. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.

Disclosure of Conflicts of Interest

IMER requires instructors, planners, managers, and other individuals who are in a position to control the content of this activity to disclose any real or apparent conflict of interest they may have as related to the content of this activity. All identified conflicts of interest are thoroughly vetted by IMER for fair balance, scientific objectivity of studies mentioned in the materials or used as the basis for content, and appropriateness of patient care recommendations.

The faculty reported the following financial relationships or relationships to products or devices they or their spouse/life partner have with commercial interests related to the content of this CME activity:

Please refer to the individual Faculty Bio’s for statements.

The planners and managers reported the following financial relationships or relationships to products or devices they or their spouse/life partner have with commercial interests related to the content of this CME activity:

Madelyn T. Herzfeld, RN, BSN, OCN®, reported no areas of conflict.

Dorothy Dulko, PhD, RN, AOCNP-C, reported no areas of conflict.

Davecia Ragoonath, MS, reported no areas of conflict.

 

Disclaimer

Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patient’s conditions and possible contraindications on dangers in use, review of any applicable manufacturer’s product information, and comparison to recommendations of other authorities.

Sponsored by:

This activity is supported by an independent educational grant from
Genentech BioOncology

Faculty

Carrie Tompkins Stricker, PhD, RN (Chairperson)
Abramson Cancer Center of the University of Pennsylvania
  • Bio
  • Abstract 1
  • Abstract 2

Dr. Stricker is an oncology nurse practitioner within the Hematology/Oncology Division of the Abramson Cancer Center at the University of Pennsylvania, Philadelphia, where she has teaching as well as clinical responsibilities. Active within the Oncology Nursing Society (ONS), she participates in the Nursing Research Special Interest Group and the Nurse Practitioner Special Interest Group. Dr. Stricker has authored and co-authored a number of peer-reviewed articles in journals such as Cancer Practice, Blood, Oncology Nursing Forum, and Clinical Journal of Oncology Nursing.

Carrie Tompkins Stricker, PhD, RN, reported a financial interest/relationship or affiliation in the form of: Speakers’ Bureau, Merck & Company, Inc., and Roche, Inc; Contracted Research, Merck & Company, Inc.

Treatment Overview: The Therapeutic Landscape for Breast Cancer

Breast cancer is the most common type of cancer in women. Over 200,000 new cases will be diagnosed in the United States in 2007, and an estimated 40,910 deaths will be attributed to this disease. Fortunately, an explosion of new therapies has improved the outlook for the millions of women living with breast cancer. Some of the most exciting developments during the past few years have included the introduction and expansion of targeted therapies in both the adjuvant and metastatic treatment settings. Targeted therapies, which use drugs or other substances to identify and attack specific cancer cells while minimizing harm to normal cells, include trastuzumab, a monoclonal antibody against the HER2 oncogene, lapatinib, an oral dual tyrosine kinase inhibitor targeting HER1 and HER2, and bevacizumab, a monoclonal antibody targeting angiogenesis. Targeted therapies are increasingly being employed both independently and in conjunction with chemotherapy and/or hormonal therapy to improve outcomes for women with breast cancer.

Workshop: Model Algorithm for Assessing and Managing Cardiotoxicity

Consistent with their novel mechanisms of action, targeted therapies present unique challenges to oncology nurses in terms of their methods of administration and toxicity profiles; some side effects, such as cardiotoxicity, have the potential to be life threatening. This presentation will address the rationale for the use of targeted therapies, provide an overview of evolving clinical trial data, and highlight toxicity issues in the context of a case study.


Edward H. Romond, MD
Lucille Parker Markey Cancer Center University of Kentucky
  • Bio
  • Abstract

Dr. Romond is professor of medicine at the University of Kentucky College of Medicine and Markey Cancer Center. He is the study chair for the National Surgical Adjuvant Breast and Bowel Project (NSABP) and principal investigator on the NSABP B-31 trial, a recently reported pivotal trial for the treatment of women with HER2-positive primary breast cancer.

Edward H. Romond, MD, reported a financial interest/relationship or affiliation in the form of: Consultant, Genentech BioOncology.

Clinical Trials Update: Practical Applications for Oncology Nurses

The introduction of the monoclonal antibody trastuzumab 10 years ago significantly improved outcomes for women with HER2-positive metastatic breast cancer and reaffirmed the value of targeting specific key cellular proteins as an effective means of controlling disease. This has led to the development of a plethora of new agents targeting not only important steps of the HER2 pathway but also other critical elements of tumor biology such as angiogenesis. Multikinase inhibitors have changed the treatment of some traditionally chemotherapy-resistant malignancies such as renal cell carcinoma; these agents are also finding their place in the management of breast cancer. Lapatinib is a small molecule that targets both HER1 and HER2 and works intracellularly on the ATP binding site of HER molecules. Bevacizumab is a monoclonal antibody that blocks the activity of vascular endothelial growth factor; the addition of the agent to first-line paclitaxel chemotherapy has doubled progression-free survival. The combination of targeted therapies with each other and with traditional chemotherapy agents has already started to change and improve the natural history of breast cancer. However, many of these targeted therapies have toxicity profiles distinct from those of traditional chemotherapy agents, requiring oncologists and oncology nurses to be cognizant of their differences in order to provide optimal patient care.

The addition of trastuzumab to chemotherapy for the adjuvant treatment of HER2-positive breast cancer has resulted in a marked improvement in early outcome for patients and has produced absolute increases in disease-free survival at 3 years, ranging from 5% to almost 13% in various trials. The corresponding relative reductions in disease recurrence range from 33% to 52%, and statistically significant improvements in patient survival have been seen in all the large adjuvant trials. In view of these impressive benefits, a major challenge is the selection of chemotherapy regimens that minimize the well-recognized cardiac risk of trastuzumab/chemotherapy combinations while achieving the highest possible anticancer efficacy. Upcoming clinical trials, including some testing combinations of targeted agents as well as others evaluating preoperative therapies, are extremely promising and deserve wholehearted support from the oncology community as we approach the possibility of cure for HER2-positive breast cancer.

Melissa Craft, RN, PhD, AOCN®
Breast Imaging of Oklahoma
  • Bio
  • Abstract

Dr. Craft is an oncology clinical nurse specialist at Breast Imaging of Oklahoma in Edmond, Oklahoma, and is a clinical instructor at the University of Oklahoma College of Medicine in Oklahoma City, Oklahoma. She received her master’s degree in nursing from the University of Oklahoma and doctorate in nursing from Texas Women’s University in Denton, Texas. Dr. Craft has presented lectures and authored numerous journal articles on breast cancer risk factors and treatment. She is a founding member of the Oklahoma Association of Clinical Nurse Specialists and a member of the Oncology Nursing Society and American Nurses’ Association.

Melissa Craft, RN, PhD, AOCN®, reported no areas of conflict.

Workshop: Model Algorithms for Assessing and Managing Toxicities in Patients With Breast Cancer

Targeted therapies are becoming standard treatment for advanced breast cancer and early stage disease. This presentation focuses on the most frequent and serious toxicities of targeted therapies used in breast cancer, with recommendations for recognition, prevention, and management. The agents that will be discussed are bevacizumab, sunitinib, and sorafenib.

Approximately 25% of newly developed drugs for cancer are oral agents. Adherence to oral regimens has been studied in many chronic diseases, including hypertension, diabetes, and arthritis. Studies suggest that adherence rates in cancer treatment may be as low as 20%. Management of patients receiving oral therapies presents complex issues, including assessment of adherence and identification of complications without the benefit of frequent office visits. Achieving agreed-upon treatment goals and adherence to treatment (concordance) involves patient education, appropriate side-effect management, and personalization of therapy. Strategies for achieving success with oral therapies will be presented.

 

 

Accreditation Statements

This educational activity for 2.0 contact hours will be provided by the Institute for Medical Education & Research (IMER). IMER is an approved provider of continuing education by the Georgia Nurses Association, an accredited approver by the American Nurses Credentialing Center’s Commission on Accreditation.

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IMER affirms that the content and format of its CE activities and related materials promote improvements and quality in healthcare and do not promote a specific proprietary business interest of a commercial entity. To this end, IMER employs several strategies to ensure the absence of commercial bias, including but not limited to review of all planned content for CE activities sponsored by IMER to ensure adherence to the American Nurses Credentialing Center’s criteria and operational requirements and the Accreditation Council for Continuing Medical Education’s content validation statements and resolution of any actual or perceived conflict of interest that exist. We employ three metrics as we review your materials:

1. Fair balance
a. Recommendations or emphasis must fairly represent and be based on a reasonable and valid interpretation of the information available on the subject matter
b. No single product or service is overrepresented when other equal competing products or services are available for inclusion

2. Scientific objectivity of studies mentioned in the materials or used as the basis for content

3. Appropriateness of patient care recommendations made to learners

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