![]() |
| Home > Colorectal Cancer | |||||||
|
FacultyCarol S. Viele, MS, RN, CNS (Chairperson)
University of San Francisco Medical Center
Ms. Viele is a clinical nurse specialist in hematology/oncology/bone marrow transplant, and assistant clinical professor in the Department of Physiological Nursing at the University of California, San Francisco (UCSF). She received her BSN and MS from the University of Michigan, Ann Arbor, and is licensed as a registered nurse in Michigan, Missouri, and California. Carol S. Viele, MS, RN, CNS, has a financial interest/relationship or affiliation in the form of: Speakers’ Bureau, Novartis Inc., Merck & Co., Inc., sanofi-aventis U. S., MedImmune, Inc., & Pfizer, Inc. The Role of Fluoropyrimidines in Colorectal Cancer Treatment: Past, Present, and FutureColorectal cancer (CRC) is a significant health issue for the American population. It is the third most common malignancy in both men and women. Because this disease is so common, it has been a research priority to develop new treatment modalities. New agents have been discovered throughout the last decade, and this has led to longer survival and an enhanced quality of life for patients with CRC. In the current treatment armamentarium, there are multiple agents that are used at variable doses and schedules, each having unique toxicities. Using a case-based approach, this program will focus on two of the most common toxicities experienced by patients undergoing therapy for CRC: diarrhea and mucositis, which may lead to significant distress and a decrease in quality of life. Case presentations will illustrate the side-effect profile and pathophysiology of diarrhea and mucositis, along with the most current evidence-based literature to treat and manage them. Nursing interventions and patient education information will also be described. Nursing plays a unique role in side-effect management because patients will frequently discuss these two side effects with their nurse but will be reluctant to discuss them with the physician due to their fear of treatment being held or permanently discontinued. This program will provide nurses with the most up-to-date literature and treatment information to manage these side effects while allowing patients to continue therapy.
Edward Chu, MD
Yale Cancer Center
Dr. Chu is professor of medicine and pharmacology at the Yale University School of Medicine in New Haven, Connecticut. He received his docter of medicine from Brown University, where he also completed his residency training in internal medicine. Dr. Chu’s research focuses on the design and development of novel treatments for colorectal and other cancers. His studies have provided insights into how tumors become resistant to the effects of chemotherapy. Dr. Chu is the founding editor-in-chief of the journal Clinical Colorectal Cancer. Edward Chu, MD, has a financial interest/relationship or affiliation in the form of: Consultant, Roche Laboratories, Inc, Pfizer Inc., Bristol-Myers Squibb Company, & ImClone Systems Incorporated. Case Studies of Fluoropyrimidine Use in Colorectal Cancer: Oncology Nursing Implications for Chemotherapy-Induced Diarrhea and Oral MucositisColorectal cancer (CRC) is a worldwide public health problem with nearly one million new cases diagnosed each year, resulting in approximately 500,000 deaths. In the United States, it is the second leading cause of cancer mortality, and approximately 52,000 deaths will be attributed to this disease in 2007. Chemotherapy has been the mainstay approach for patients with advanced CRC. For nearly 40 years, the fluoropyrimidine 5-fluorouracil (5-FU) was the primary drug used to treat patients with CRC, and 2007 marks the 50th anniversary of the synthesis of this agent. Within the past two decades—and especially within the past 5 years—significant advances have been made in treatment options. Since the late 1990s, the United States Food & Drug Administration (FDA) approved three new chemotherapeutic agents for the treatment of CRC: irinotecan, oxaliplatin, and capecitabine; and within the last 3 years, it has approved three novel biologic agents: the antiepidermal growth factor receptor antibodies cetuximab and panitumumab, and the antivascular endothelial growth factor bevacizumab. With the increasing availability of active treatments for patients with metastatic CRC, there are several important issues that must be addressed on a daily basis, including optimal cytotoxic chemotherapy regimen, the role of oral versus intravenous 5-FU chemotherapy as the backbone for combination regimens, continuous versus intermittent chemotherapy, and the integration of targeted therapies with cytotoxic chemotherapy regimens. Pamela Hallquist Viale, MS, RN, CS, ANP, AOCNP®
University of California, San Francisco
Ms. Viale is an assistant clinical professor in the Department of Physiological Nursing at the UCSF. She received her master’s degree in oncology nursing and her post-master’s adult nurse practitioner certificate from UCSF. Ms. Viale has lectured nationally on oncology nursing subjects, authored journal articles on oncology nursing, and presented at local and national Oncology Nursing Society (ONS) meetings. She recently served as the associate editor for nursing education for the ONS Web site and is a member of the editorial advisory board for the ONCOLOGY Nurse Edition publication. Ms. Viale also serves as an expert panel member for the ManageCRC.com Web site, which provides information on CRC for nursing professionals. Pamela Hallquist Viale, MS, RN, CS, ANP, AOCNP®, has a financial interest/relationship or affiliation in the form of: Consultant, Institute for Medical Education & Research, Novartis, Inc., and Meniscus Limited; Speakers’ Bureau, Institute for Medical Education & Research, Novartis, Inc., Meniscus Limited, Amgen, Inc., Merck & Co., Inc., & Bristol-Myers Squibb Company. Palmar-Plantar Erythrodysesthesia and Compliance With Oral Chemotherapy: Case Studies and Management StrategiesOncology nurses are paramount in the successful management of patients receiving fluoropyrimidine therapy, which is commonly given in the forms of either continuous and bolus 5-fluorouracil (5-FU) or oral capecitabine, a prodrug of 5-FU. By changing the method of administration for 5-FU, the side-effect profile of the drug is also altered. Bolus 5-FU is associated with myelosuppression, diarrhea, and mucositis, while administering the drug in continuous infusion causes palmar-plantar erythrodysesthesia (PPE) or hand-foot syndrome. Oral administration of capecitabine, while associated with myelosuppression, diarrhea, and mucositis, can cause PPE as well, and it is known as a dose-limiting side effect of this form of chemotherapy, necessitating dosage reductions or even interruption of therapy if patients develop greater than a grade 1 toxicity. Because capecitabine is an orally administered therapy, adherence can be a problem. Historically, adherence to medications in chronic illness runs approximately 50% (Osterberg & Blaschke, 2005). In patients with cancer, one might assume that adherence would be 100% given the seriousness of the diagnosis, however there are clinical trial data showing that patients with cancer are often nonadherent to medication administration.Women on tamoxifen have been shown to have reduced adherence with medication administration, and adherence continues to drop steadily with each year of drug therapy (Partidge, Wang, Winer, & Avorn, 2003). This nonadherence has also been noted with chemotherapy agents such as cyclophosphamide (Lebovits et al.,1990). As the use of oral therapies increases, adherence becomes even more important. Strategies for improving adherence to oral antineoplastic agents have been discussed and oncology nurses should employ them with patients who are prescribed oral therapies. These strategies include reinforcement of patient education, the use of pill counts, calendars, patient diaries, and improved communication (Moore, 2007; Viele, 2007; Osterberg, & Blaschke, 2005). This presentation will discuss background on both PPE and adherence to medications and will use case studies to illustrate management strategies.
DisclaimerParticipants 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.
Safeguards Against Commercial BiasIMER 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
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 Privacy PolicyWhen you participate in an educational activity provided by the Institute for Medical Education & Research (“IMER” or “we”), we ask you for your name, degree, affiliation, street address, telephone number, fax number, and e-mail address (the “Information”). We use that Information in the following ways: We use the Information to grade your posttest and to send you a certificate of completion of the educational activity. If we use a third-party company to grade your posttest and issue certificates of completion, we will give the Information to that company for that purpose only. For each educational activity that you take, you must complete an evaluation questionnaire. That questionnaire asks if you are willing to participate in a follow-up survey. If you answer yes, we will use your name and contact information to send you the survey. We may use the Information to invite you to participate in other educational activities that IMER or its affiliates may offer. On occasion, the commercial supporter of a educational activity will ask us for a list of the people who participated in that activity, so that it may document the first level of outcomes-based evaluation in the educational activity (i.e., who attended, which medical specialties/practices were represented, how this compares to the target audience, and whether the activity needs to be repeated because significant numbers of the target audience did not attend). In that event, we will provide the supporter with your name, title and affiliation, but we will request in writing that the supporter not contact you directly for any purpose. If our company is acquired or merged into another company, we may make the Information available to the new owner/entity to use in the ways described above, to enable it to continue our business. Any changes to our privacy policy will be posted here. Method of ParticipationThere are no fees for participating and receiving nursing contact hours for this activity. Participants must complete the posttest by recording the best answer to each question. Once you finished your test and completed the subsequent evaluation form, click submit test to send your responsed to us. Your test will be immediately reviewed and if you receive a passing grade of 70% or better, you will then be directed to print your certificate online.MediaWeb site |
||||||
© Copyright 2003 – 2008 Institute for Medical Education & Research, Inc. All Rights Reserved.