Harnessing Novel Treatment Paradigms for Metastatic Colorectal Cancer
The landscape of mCRC management has been extensively and rapidly altered by the identification of a wide swath of targetable tumor biomarkers, and advancements in knowledge continue to progress rapidly. In response, a large number of therapies targeted to these genetic alterations have swiftly emerged, with many more about to enter the treatment landscape. These therapies encompass many diverse mechanisms of action, with distinct and varied consequences for patient selection, agent sequencing, and AE management. Clinicians who treat patients with mCRC have to not only understand the implications that each agent has for discrete patient populations, the latest clinical data surrounding their application, and best-practice management strategies for treatment-related toxicities, but also the importance of genomic testing and the latest recommendations concerning its application to patients with mCRC in order to effectively leverage the full armamentarium of agents. Information and guidance concerning the treatment of mCRC is swiftly evolving, making it challenging for clinicians to keep up to date with the latest advancements in treatment.
This webcast focuses on the latest clinical data including novel treatment options for metastatic colorectal cancer.
Provided by North American Center for Continuing Medical Education, LLC (NACCME), an HMP Company.
For questions regarding this educational activity, please call 609-371-1137 or email firstname.lastname@example.org.
This educational activity is designed to meet the educational needs of those who are involved and/or interested in the treatment of patients with GI cancers, community oncologists, physicians, physician assistants, physicians-in-training, oncology nurses, and pharmacists.
After participating in this activity, learners should be better able to:
- Review the current landscape of genomic biomarkers in CRC, their prognostic significance, and updated recommendations for patient testing
- Appraise the safety/efficacy profiles and clinical implications of current and emerging targeted agents for the treatment of metastatic CRC
- Analyze novel pan-tumor agents used in metastatic CRC
To be eligible for credit, participants must complete the online activity and the evaluation. Upon completing the activity, there will be instructions on how to complete the evaluation and print a certificate or other documentation of credit.
Release Date: November 29, 2021
Expiration Date: November 29, 2022
Estimated Time to Complete: 200 minutes
There is no fee associated with this activity.
Supported by educational grants from: Bayer Healthcare Pharmaceuticals, Inc., Pfizer Inc., and Taiho Oncology, Inc.
In support of improving patient care, this activity has been planned and implemented by North American Center for Continuing Medical Education (NACCME) and Imedex. NACCME is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
NACCME designates this internet enduring activity for a maximum of 3.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
American Academy of Nurse Practitioners National Certification Program accepts AMA PRA Category 1 Credit™ from organizations accredited by the ACCME.
This continuing nursing education internet enduring activity awards 3.5 contact hours.
Provider approved by the California Board of Registered Nursing, Provider #13255 for 3.5 contact hours.
This internet enduring, knowledge-based activity (Universal Activity Number: JA0006201-9999-21-203-H01-P) has been approved for a maximum of 3.5 contact hours (0.350 CEUs).
The certificate is not the official record of your participation in the activity. The official record of credit will be the information in the CPE Monitor system. Following ACPE Policy, NACCME must transmit your claim to CPE Monitor within 60 days from the date you complete this CPE activity. NACCME is not able to report your claimed credit after this 60-day period. Eligibility for pharmacy credit is contingent upon the successful completion of a post-test and/or evaluation for each activity or session attended.
NACCME has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with the AAPA CME Criteria. This internet enduring activity is designated for 3.5 AAPA Category 1 credits. PAs should only claim credit commensurate with the extent of their participation.
USE OF PROPRIETARY NAMES
This continuing medical education activity may include device or medicine brand names for participant clarity purposes only, due to the presence of different branded versions of the same product. No product promotion or recommendation should be inferred.
UNAPPROVED AND/OR INVESTIGATIONAL USES OF DRUGS AND DEVICES
This activity may contain information about experimental and other uses of drugs or devices that are not currently approved by the European Medicines Agency (EMA) of the European Union or the Food and Drug Administration (FDA) of the United States. Participants are strongly encouraged to consult approved product labeling for any drug or device mentioned in this activity before use. The opinions expressed during this activity are the opinions of the respective authors, presenters or moderators and do not necessarily reflect the opinions of NACCME.
The material presented and related discussions are not intended to be medical advice, and the presentation or discussion of such material is not intended to create and does not establish a physician-patient relationship. Medical advice of any nature should be sought from an individual’s own physician.
Neither NACCME nor any of its subsidiaries or affiliates is affiliated with, or formally endorsed by a medical society.
The opinions expressed in this educational activity are those of the faculty and are not attributable to NACCME or HMP. Clinical judgment must guide each professional in weighing the benefits of treatment against the risk of toxicity. Dosages, indications, and methods of use for products referred to in this activity are not necessarily the same as indicated in the package insert for each product, may reflect the clinical experience of the presenters, and may be derived from the professional literature or other clinical sources. Consult complete prescribing information before administering.
DISCLOSURE OF RELEVANT FINANCIAL RELATIONSHIPS
NACCME, LLC is an independent provider(s) of continuing medical education. NACCME, LLC has no proprietary or financial interest in medical or healthcare products over which the FDA (USA) or EMA (EU) has regulatory authority.
NACCME, LLC assures that all educational materials are reviewed to ensure for the absence of commercial bias, fair balance, scientific objectivity, and levels of evidence. The educational activity will not be influenced by commercial organizations and will not conflict with any other scheduled educational activities.
According to the disclosure policy of NACCME, faculty, editors, managers, and other individuals who are in a position to control content are required to disclose any relevant financial relationships with relevant commercial companies related to this activity. All relevant conflicts of interest that are identified are reviewed for potential conflicts of interest. If a conflict is identified, it is the responsibility of NACCME to initiate a mechanism to resolve the conflict. The existence of these interests or relationships is not viewed as implying bias or decreasing the value of the presentation.
The faculty has reported the following:
Eric Van Cutsem: Grant/Research Support-Amgen, Bayer, Boehringer Ingelheim, BMS, Celgene, Ipsen, Lilly, Merck Sharp & Dohme, Merck KGaA, Novartis, Roche, Servier; Advisory Board-Array, AstraZeneca, Bayer, Biocartis, BMS, Celgene, Daiichi Sankyo, Halozyme, GSK, Pierre-Fabre, Incyte, Ipsen, Lilly, Merck Sharp & Dohme, Merck KGaA, Novartis, Pierre Fabre, Roche, Servier, Sirtex, Taiho Pharmaceutical
In addition to the faculty listed below, NACCME and Imedex planners and staff include Samantha Conforti, Kelly Jackson, Mary Johnson, Amanda Mulder, Paul O'Neil, Randy Robbin, Manjusha Sala, and Greaton Sellers.
No NACCME or Imedex planner or staff has disclosed any relevant financial relationship with any ineligible company (commercial interest).
North American Center for Continuing Medical Education (NACCME) complies with the legal requirements of the Americans with Disabilities Act and the rules and regulations thereof. If any participant in this educational activity is in need of accommodations, please call 609-371-1137.
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Copyright © 2021 by North American Center for Continuing Medical Education, LLC. All rights reserved. No part of this accredited continuing education activity may be reproduced or transmitted in any form or by any means, electronic or mechanical, without first obtaining permission from North American Center for Continuing Medical Education.
Any participant wanting to file a grievance with respect to any aspect of a continuing education activity accredited by NACCME, LLC may contact Samantha Conforti, Manager, Accreditation and Compliance, by phone at 609-371-1137, by email at email@example.com or in writing at 104 Windsor Center Drive, East Windsor, NJ 08520. Ms. Conforti will review the grievance and respond within 30 days of receiving the complaint. If the participant is unsatisfied with the response, an appeal to the Associate Director, Greaton Sellers, Accreditation and Compliance, can be requested for a second level of review. Mr. Sellers can be contacted via email at firstname.lastname@example.org.