Immunotherapy has radically transformed the landscape of frontline treatment for advanced non-small cell lung cancer (NSCLC) without actionable mutations. Join us for this live event to hear our expert panel offer privileged insights into evidence-based guidelines for biomarker testing, the latest data pertaining to therapeutic options for NSCLC with high PD-L1 expression, and strategies to address immune-related adverse events. A patient with history of advanced NSCLC will be on the panel to augment these insights with “teaching moments” from his treatment journey.
Upon completion of this activity, participants should be better able to:
Chair and Professor, Medical Oncology
University Hospital of Lausanne
Honorary Chair, Department of Pathology
Aberdeen University School of Medicine
Aberdeen Royal Infirmary
Aberdeen, Scotland, United Kingdom
Professor, Hematology and Medical Oncology
Roberto C. Goizueta Chair, Cancer Research
Director, Division of Medical Oncology
Assistant Dean, Cancer Research
Deputy Director, Winship Cancer Institute
Emory University School of Medicine
Atlanta, Georgia, United States
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity do not recommend the use of any agent outside of the labeled indications. The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of the planners. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
Participants 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 and/or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
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