Greater understanding of the tumor microenvironment of nasopharyngeal carcinoma (NPC) has led to the introduction of immunotherapy into the NPC treatment landscape. Incorporating immunotherapy has changed the current standard of care in the treatment of recurrent and metastatic NPC. Robert Ferris, MD, explores clinical trial data leading to approval of PD-1 inhibitors both as monotherapy and in combination with chemotherapy. He also delves into the significance of biomarkers that may influence prognosis and management of patients with NPC, as well as managing toxicity related to PD-1 inhibitors.
Course Credit:
0.5 AMA PRA Category 1 CreditsTM
Dates:
Opens: 2024-10-07
Closes: 2025-10-07
Target Audience:
This activity is intended for medical oncologists, head and neck surgeons, radiation oncologists, physician associates, nurse practitioners, nurses, and pharmacists involved in the care of patients with metastatic nasopharyngeal carcinoma (NPC).
This activity is supported by a grant from Coherus Biosciences.
Accreditation
The Annenberg Center for Health Sciences at Eisenhower designates this enduring activity for a maximum of 0.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Additional Content Planners
Rachel Feaster, PharmD, BCOP (Medical Writer)No significant relationships to disclose.
Annenberg Center for Health Sciences
Staff at the Annenberg Center for Health Sciences at Eisenhower have no relevant financial relationships to disclose.
All of the financial relationships listed for these individuals have been mitigated.
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Robert Ferris, MD, PhD
Associate Senior Vice Chancellor for Cancer Research, Health Sciences
Hillman Professor of Oncology
Professor of Otolaryngology, of Immunology, and of Radiation Oncology, School of Medicine
Director, UPMC Hillman Cancer Center
Pittsburgh, Pennsylvania
Presenting Faculty
Learning Objectives
- Design evidence-based treatment plans for patients with NPC who are appropriate candidates for immunotherapy.
- Describe the safety and efficacy of immunotherapy for patients with NPC.
- Employ appropriate biomarker testing to guide prognosis and management of patients with NPC.
- Develop appropriate collaborative strategies among the multidisciplinary and interprofessional care team to prevent, identify, and mitigate toxicities related to immunotherapy for the treatment of patients with NPC.
Faculty Disclosures
Robert Ferris, MD, PhD
Advisory Board: Adaptimmune, Bristol-Myers Squibb, Coherus BioSciences, Inc., CureVac, Eisai Europe Limited, Genmab, Hookipa Biotech GmbH, Instil Bio, Inc, Lifescience Dynamics Limited, MacroGenics, Inc., MeiraGTx, LLC, Merck, Merus NV, Numab Therapeutics AG, OncoCyte Corporation, Pfizer, Rakuten Medical, Inc, Regeneron, Seagen, Inc, SIRPant Immunotherapeutics, Inc, Vir Biotechnology, Inc
Board of Directors: CytoAgents
Consultant: Adagene Incorporated, Aduro Biotech, Inc., Bicara Therapeutics, Inc, Brooklyn ImmunoTherapeutics LLC, Catenion, EMD Serono, Everest Clinical Research Corporation, F. Hoffmann-La Roche Ltd, Federation Bio, Inc, Genocea Biosciences, Inc, Kowa Research Institute, Inc., Mirati Therapeutics, Inc, Nanobiotix, Novartis Pharmaceutical Corporation, Novasenta, PPD Development, L.P., Sanofi, Zymeworks, Inc.
Data Safety Monitoring Board: Mirror Biologics, Inc.
Research Support: Bristol-Myers Squibb, AstraZeneca/MedImmune, Novasenta, Tesaro