GI Cancer: Sequential Treatment Planning in the Community Oncology Setting
Please choose a module from the options below. To receive credit and a certificate, you must complete all of the modules in this activity.
Welcome to this Med-IQ Select on sequential treatment planning in the community oncology setting. Med-IQ Select is a unique online educational offering that allows you to pick and choose the content you would like to view—in any order and at your convenience.
To get started, click "view" on any of the modules below. To receive credit and a certificate, you must complete all of the modules.
Time to complete: 13 minutes
Time to complete: 26 minutes
Time to complete: 13 minutes
Time to complete: 8 minutes
Time to complete: 5 minutes
Time to complete: 16 minutes
Complete all of the above modules to earn credit;
0 out of 6 modules complete
Tanios S. Bekaii-Saab, MD
Professor of Medicine
Vice Chair and Section Chief, Division of Hematology/Oncology
Department of Internal Medicine
College of Medicine and Science
Leader, Gastrointestinal Cancer Program
Mayo Clinic Cancer Center
Medical Director, Cancer Clinical Research Office
Johanna Bendell, MD
Chief Development Officer
Director, Drug Development Unit Nashville
Sarah Cannon Research Institute
Axel Grothey, MD
Director GI Cancer Research
West Cancer Center and Research Institute
David H. Ilson, MD, PhD
Memorial Sloan Kettering Cancer Center
New York, NY
Amy Burdette, PhD
Manager, Educational Strategy and Content
Kathryn Schaefer, MSN, RN, CPHRM
Senior Manager, Accreditation and Compliance
East Lansing, MI
Upon completion, participants should be able to:
- Use patient characteristics and biomarker profiles to inform treatment decisions for patients with advanced or metastatic gastric and GEJ cancer
- Select appropriate treatment regimens for patients with advanced or metastatic gastric and GEJ cancer that maximize the benefit of sequential lines of therapy
- Define the influence of molecular characteristics and primary tumor location on treatment effectiveness in patients with mCRC
- Optimally select and sequence treatments for patients with mCRC based on multiple clinical factors including molecular characteristics and primary tumor location
- Discuss the use of prognostic and predictive biomarkers including AFP in HCC
- Identify patients with advanced HCC who would benefit from individualized treatment approaches
This activity is intended for community oncologists.
Statement of Need
Knowledge related to the genetic nature of gastrointestinal (GI) cancers—specifically metastatic colorectal cancer (CRC), gastric and gastroesophageal junction (GEJ) adenocarcinoma, and hepatocellular carcinoma (HCC)—as well as the use of biomarkers in patients with these cancers when appropriate, is rapidly evolving, requiring community oncologists to stay abreast of emerging evidence to guide treatment planning. Evidence-based guidelines and ongoing research can provide frameworks for determining treatment selection and proper sequencing across multitudes of different combinations of chemotherapy, molecular targeted therapies, anti-angiogenic agents, and immunotherapies; however, the most effective selection and sequence of agents continues to be debated. Focused, contextual education can help community oncologists better understand the role of factors such as patient characteristics and anatomical and molecular profiles of tumors in determining first-line treatment and subsequent lines of therapy.
Provided by Med-IQ.
Med-IQ is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
Med-IQ designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Nurse practitioners, physician assistants, and other healthcare professionals who successfully complete the activity will receive a Statement of Participation indicating the maximum credits available.
Medium/Method of Participation
This is a 1.5-credit CME activity. To receive credit, read the introductory CME material, complete all of the modules, and complete the evaluation, attestation, and post-test, answering at least 70% of the post-test questions correctly.
Initial Release Date: August 9, 2019
Expiration Date: August 8, 2020
Estimated Time to Complete This Activity: 1 hour and 30 minutes
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The content of this activity has been peer reviewed and has been approved for compliance. The faculty and contributors have indicated the following financial relationships, which have been resolved through an established COI resolution process, and have stated that these reported relationships will not have any impact on their ability to give an unbiased presentation.
Tanios S. Bekaii-Saab, MD
Consulting fees/advisory boards: AbbVie Inc., Imugene, Immuneering Corporation
Other: ARMO Biosciences, Exelixis, Inc., SillaJen Inc.
Johanna Bendell, MD, has indicated no real or apparent conflicts.
Axel Grothey, MD, has indicated no real or apparent conflicts.
David H. Ilson, MD, PhD
Consulting fees/advisory boards: Amgen, Astellas Pharma US, Inc., AstraZeneca, Bayer HealthCare Pharmaceuticals, Bristol-Myers Squibb, Eli Lilly and Company, F. Hoffman-La Roche Ltd., Merck & Co., Inc., Pieris Pharmaceuticals, Taiho Pharmaceutical Co, Ltd.
Contracted research: Astellas Pharma US, Merck & Co., Inc., Pieris Pharmaceuticals, Taiho Pharmaceutical Co, Ltd.
The peer reviewers and activity planners have no financial relationships to disclose.
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This activity is supported by an educational grant from Lilly. For further information concerning Lilly grant funding visit www.lillygrantoffice.com.
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