This program has expired; CME credits no longer available.
Chief Complaint:
Fatigue and leg swelling
History of Present Illness:
Martin returns to his hematologist for a routine follow-up visit complaining of increasing lethargy and fatigue, achiness, nausea, constipation and swelling of his legs. Subsequent to a diagnosis of multiple myeloma 8 months prior, he received induction therapy with thalidomide plus dexamethasone (Thal/Dex), and then underwent successful autologous stem cell transplantation (ASCT). He achieved a Very Good Partial Response (VGPR) and has since continued therapy with thalidomide/dexamethasone with routine monitoring at three-month intervals.
Although prophylactic warfarin was initiated with induction therapy, Martin has had difficulty regulating his INR. Between visits, he has also become increasingly fatigued, especially when faced with routine chores around the house. Other complaints include a decreased appetite and mild nausea throughout the day, urinary frequency (7-8 times daily), and leg swelling during the past week, more so on the right. He attributes an ongoing achiness in his shoulders, lower back and legs, all independent of physical activity, to a viral syndrome.
Accreditation Statement:
MedCases, LLC is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education.
Policy on Speaker and Provider Disclosure:
As a provider accredited by the Accreditation Council for Continuing Medical Education (ACCME), it is the policy of MedCases to require the disclosure of the existence of any significant financial interest or any other relationship a faculty member or a provider has with the manufacturer(s) of any commercial product(s) discussed in an educational presentation. The presenting faculty reported the following.
| Kenneth C. Anderson, MD | Consultant and Grant/Research Support: Celgene Corporation, Millennium Pharmaceuticals, Novartis Pharmaceuticals |
| Ruben Niesvizky, MD | Speakers Bureau: Celgene Corporation, Millennium Pharmaceuticals, Novartis Pharmaceuticals, Ortho Biotech
Grant/Research Support: Celgene Corporation, Millennium Pharmaceuticals
Consultant: Millennium Pharmaceuticals |
| Steven T. Rosen, MD, FACP | Consultant: Abbott Laboratories, Allos Therapeutics, Berlex Laboratories, Biocryst Pharmaceuticals, Celgene Corporation, Cell Therapeutics Inc, Genentech Inc, Genta, Ligand Pharmaceuticals, Eli Lilly and Co, Pharmion Corporation, Sigma-Tau Pharmaceuticals, SuperGen, Therakos Inc, Wyeth |
| G. David Roodman, MD, PhD | Consultant: Acceleron Pharma, Amgen Inc, Celgene Corporation
Consultant, Speakers’ Bureau, Grant/Research Support: Novartis Pharmaceuticals |
| Planning Committee Members |
| Dorothy Schirf, MD | Stockholder: Alkermes, Inc, Ligand Pharmaceuticals, Northfield Laboratories, Inc, Pfizer, Inc |
Harvey Mossman, MD; Carolyn Darrow, MPH; and Sharon Barnett have indicated that they have not received financial support for consultation, research, or, evaluation, or have a financial interest relevant to this online activity.
Method of Participation:
This Internet-based activity takes approximately 2 hours to complete. You should review the important information on this page, check the box below and click the button to proceed to the case. First-time visitors will be asked to complete their profile. After completing the activity you will answer a multiple-choice post-test and complete an evaluation form online. Once completed, you will be able to save your certificate to your own computer and print it on your own printer.
Statement of Responsibility:
MedCases takes responsibility for the content, quality, and scientific integrity of this CME activity.
Course Director and Principal Faculty:
Kenneth C. Anderson, MD (CO-CHAIR)
Kraft Family Professor of Medicine
Harvard Medical School
Chief, Division of Hematologic Neoplasia
Director, Jerome Lipper Multiple Myeloma Center
Dana-Farber Cancer Institute
Boston, MA
Ruben Niesvizky, MD (CO-CHAIR)
Director, Multiple Myeloma Program
Center of Excellence for Lymphoma and Myeloma
New York Presbyterian Hospital – Cornell University
New York, NY
Steven T. Rosen, MD, FACP
Genevieve Teuton Professor of Medicine
Feinberg School of Medicine
Director
Robert H. Lurie Comprehensive Cancer Center
Northwestern University
Chicago, IL
G. David Roodman, MD, PhD
Professor of Medicine
Vice Chair for Research
Director, Myeloma Program at UPMC
University of Pittsburgh
Pittsburgh, PA
Target Audience:
This activity is intended for hematologists and community oncologists.
Prerequisites:
There are no prerequisites
Statement of Need:
Significant progress has been made in diagnosis, assessment, and treatment of patients with multiple myeloma. The utilization of new classes of therapy, as well as improved strategies for managing toxicities of these medications, have resulted in new and more effective options that can prolong disease control and survival. Clinicians are now able to change the traditional goals to a more ambitious objective of achieving a complete response, in the hopes of longer progression-free survival and improved quality of life for their patients. Further, the need for stem cell transplants and the potential for associated medical complications may continue to diminish based on the potential for achieving complete remissions with combination therapy in newer protocols.
However, healthcare practitioners are faced with overcoming several clinical barriers quickly to achieve optimal outcomes in their patients. The rapidity of change in this continually evolving arena may cause delays incorporating newer evidence into clinical practice. Lack of familiarity with the newer protocols and the mechanisms of action of newer agents, the potential for adverse effects, and concerns about management of toxicities are all important obstacles in updating the clinical paradigms. Overcoming these obstacles will enable physicians to apply updated guidelines and current evidence to improve the quality of care for multiple myeloma patients.
Objectives:
On completing this activity, you should be able to:
- Execute diagnostic and monitoring protocols appropriate for progressive myeloma
- Implement standard therapy of progressive myeloma in the context of common comorbidities
- Successfully manage major therapeutic toxicities of myeloma patients
Off-label Statement/Unapproved Uses:
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No faculty member has indicated that their presentation will include information on off-label products.
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