Launch Date
12/01/2020
Credit Amount
0.00 Expired
Credit Expires
12/01/2021
The discovery of molecular alterations that drive tumor initiation and progression has revolutionized the treatment strategy for non-small cell lung cancer (NSCLC) by matching targeted therapies to a specific mutation, leading to significantly improved therapeutic efficacy. However, despite the initial effectiveness of targeted therapy for NSCLC, most patients ultimately develop acquired resistance with subsequent disease progression, making it imperative for clinicians to receive up-to-date education on evaluating new therapeutic options to improve outcomes and better tailor treatment strategies.
In this CME Outfitters Live and OnDemand, integrations of animated 3-D models will provide visual representation of the mechanisms and characteristics of antibody drug conjugates (ADCs) in NSCLC to complement expert faculty insights and evidence supporting testing strategies to identify predictive biomarkers, emerging treatment options for advanced or metastatic NSCLC, and best practices for managing patients with lung cancer in the face of COVID-19 and beyond.
At the end of this CME/CE activity, participants should be able to:
The following learning objectives pertain only to those requesting CNE or CPE credit:
Supported by an educational grant from Daiichi Sankyo, Inc.
Hematology/oncology specialists, surgeons, pathologists, nurse practitioners, PAs, nurses, and pharmacists.
It is the policy of CME Outfitters, LLC, to ensure independence, balance, objectivity, and scientific rigor and integrity in all of their CE activities. Faculty must disclose to the participants any relationships with commercial companies whose products or devices may be mentioned in faculty presentations, or with the commercial supporter of this CE activity. CME Outfitters, LLC, has evaluated, identified, and attempted to resolve any potential conflicts of interest through a rigorous content validation procedure, use of evidence-based data/research, and a multidisciplinary peer review process. The following information is for participant information only. It is not assumed that these relationships will have a negative impact on the presentations.
Dr. Borghaei reports he receives research support from Bristol-Myers Squibb Company/Eli Lilly and Company and Merck & Co./Celgene Corporation. He is on the advisory committee for AbbVie Inc.; Amgen Inc.; AstraZeneca; Axiom Healthcare Services; BioNTech; Boehringer Ingelheim; Bristol-Myers Squibb Company; Cantargia AB; Celgene Corporation; Daiichi Sankyo, Inc.; Eli Lilly and Company; EMD Serono, Inc.; Genentech, Inc.; Genmab; GLG; HUYA Bioscience International; Merck & Co.; Novartis; Pfizer Inc.; PharmaMar; Regeneron Pharmaceuticals Inc.; and Takeda Pharmaceuticals U.S.A., Inc. He is a consultant for Amgen; AstraZeneca; Bristol-Myers Squibb Company; Daiichi Sankyo, Inc.; EMD Serono, Inc.; and PharmaMar. He receives other financial or material support from Data and Safety Monitoring Board: Incyte; Takeda Pharmaceuticals U.S.A., Inc. and University of Pennsylvania. He is on the scientific advisory board for Rgenix (stock options) and Sonnet BioTherapeutics, Inc. (stock options).
Dr. Felip reports she receives research funding from Fundación Merck Salud and a grant for Oncology Innovation (GOI) EMD Serono. She serves in a advisory role or speakers bureau for for AbbVie Inc.; Amgen Inc.; Astra Zeneca, Bayer, Blueprint Medicines Corporation; Boehringer Ingelheim; Bristol-Myers Squibb Company; Eli Lilly and Company; F. Hoffmann-La Roche; GlaxoSmithKline; Janssen Global Services; Merck KGaA; Merck Sharp & Dohme Corp.; Novartis; Pfizer Inc.: Puma Biotechnology, Inc.; Sanofi Genzyme, Springer; and Takeda Pharmaceutical Company. She recieves other financial or material support from Grifols (independent board member).
Dr. Geber reports he receives research support from AstraZeneca; BerGenBio; Bristol-Myers Squibb Company; and Karyopharm. He is a consultant for Bristol-Myers Squibb Company; Catalyst Pharmaceuticals, Inc.; G1 Therapeutics, Inc.; Karyopharm; and Samsung Bioepis. He is a stock shareholder (directly purchased) in Gilead Sciences, Inc.
Poshala Tish Aluwihare, PhD (planning committee) has no disclosures to report.
Howard Bliwise, MD (peer reviewer) has no disclosures to report.
Mae Ochoa, RPh (peer reviewer) has no disclosures to report.
Susan Perry (planning committee) has no disclosures to report.
Jan Perez (planning committee) has no disclosures to report.
Sharon Tordoff (planning committee) has no disclosures to report.
Disclosures were obtained from the CME Outfitters, LLC staff: No disclosures to report.
Faculty of this CE activity may include discussions of products or devices that are not currently labeled for use by the FDA. The faculty have been informed of their responsibility to disclose to the audience if they will be discussing off-label or investigational uses (any uses not approved by the FDA) of products or devices.
Post-tests, credit request forms, and activity evaluations must be completed online (requires free account activation), and participants can print their certificate or statement of credit immediately (75% pass rate required). This website supports all browsers except Internet Explorer for Mac. For complete technical requirements and privacy policy, visit our Privacy & Confidentiality page.
NOTE: Pharmacist CE Universal Activity Number, Enduring: 0376-0000-20-148-H01-P.