July 20, 2022 | 6:30 pm - 8:00 pm ET
Overview
The use of immune checkpoint inhibitors (ICIs) has been well established in metastatic disease, leading to their investigation for use in earlier stages of cancer. Currently, few ICIs are approved for neoadjuvant and adjuvant indications, though clinical trials are underway in melanoma, non−small cell lung cancer, renal cell carcinoma, and other malignancies. In this multidisciplinary panel discussion, experts will review efficacy and safety data supporting the role of ICIs in early-stage cancers and strategies to overcome challenges associated with their therapeutic uptake. The panelists will explore patient populations likely to benefit from early initiation of ICIs in therapy, considerations for initiation and duration of therapy, as well as criteria to determine benefit for patients. The pharmacist’s role and considerations for management of immune-related adverse effects for patients receiving ICIs in the adjuvant setting compared with the metastatic setting will also be discussed.
Target Audience
This educational program is directed toward oncology pharmacists, nurses, and physicians.
Learning Objectives
Upon completion of this activity, participants will be able to:
- Explore the current and emerging uses of immune checkpoint inhibitors (ICIs) in early stages of cancer and supportive clinical data
- Compare challenges in integrating ICIs into early-stage cancers among oncologists, oncology nurses, and oncology pharmacists
- Explain the importance of prompt immune-related adverse effect (irAE) identification in early-stage cancers
- Develop a plan to monitor and manage irAEs that incorporates collaboration among oncologists, nurses, and pharmacists on the multidisciplinary cancer care team
Jessica Michaud Davis, PharmD, BCOP, CPP
Moderator
Clinical Pharmacist Coordinator
Adult Hematology/Oncology
Levine Cancer Institute, Atrium Health
Charlotte, North Carolina
Disclosures: Advisory Board: Regeneron/Sanofi; Speakers Bureau: Exelixis, Inc.
Robert L. Ferris, MD, PhD
Director, UPMC Hillman Cancer Center
Hillman Professor of Oncology
Associate Vice Chancellor for Cancer Research
Professor of Otolaryngology, Immunology, and Radiation Oncology
Pittsburgh, Pennsylvania
Disclosures: Consultant: Adagene, Aduro Biotech, Inc, Bicara Therapeutics, Brooklyn lmmunoTherapeutics, F. Hoffmann-La Roche Ltd, Everest Clinical Research Corp, Genocea Biosciences Inc, Kawa Research Institute, Inc, Mirati Therapeutics, Inc, Nanobiotix, Novasenta, PPD Development, LP, Sanofi, Zymeworks, Inc, Catenion; Advisory Board: Merck, Numab Therapeutics AG, OncoCyte, Pfizer, Rakuten Medical, Inc, Seagen, SIRPant lmmunotherapeutics, Vir Biotechnology, Bristol Myers Squibb, Hookipa Biotech GmbH, Coherus BioSciences, Instil Bio, MacroGenics, Lifescience Dynamics Ltd; Research Funding: AstraZeneca/Medlmmune, Bristol Myers Squibb, Novasenta, Tesaro; Stock: Novasenta; Other (clinical trial): AstraZeneca/Medlmmune, Bristol Myers Squibb, Merck; Other (data safety monitoring board): Mirror Biologics, Inc.
Kristi K Orbaugh, MSN, NP, AOCNP
Adult Oncology Nurse Practitioner
Community Hospital Oncology Physicians
Indianapolis, Indiana
Disclosures: Speakers Bureau: Eli Lilly, BMS, Coherus, Sanofi, Regeneron, MorphoSys, CTI, Gilead, DSI, AstraZeneca, Pfizer.
The staff of Physicians’ Education Resource®, LLC, have no relevant financial relationships with ineligible companies.
PER® mitigated all COI for faculty, staff, and planners prior to the start of this activity by using a multistep process.
Pharmacy Times Continuing Education™ Planning Staff—Jim Palatine, RPh, MBA; Maryjo Dixon, RPh; Amy H. Seung, PharmD, BCOP, FHOPA; Abigail Dill; Susan Pordon; Brianna Winters; and Chloe Taccetta have no relevant financial relationships with commercial interests to disclose.
Anonymous peer reviewers were used as part of content validation and conflict resolution. The peer reviewers have no relevant financial relationships with commercial interests to disclose.

