Accreditation/Credit Designation
Physicians’ Education Resource®, LLC, is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
Physicians’ Education Resource®, LLC, designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
This activity, COPE Activity Number 122076, is accredited by COPE for continuing education for optometrists.
Acknowledgment of Support
This activity is supported by an educational grant from GlaxoSmithKline.
Oncology Consultations®: Collaborative Management of Ocular Toxicities in Patients with Relapsed/Refractory Multiple Myeloma
Release Date: June 30, 2021
Expiration Date: June 30, 2022
Activity Overview
The antibody-drug conjugate (ADC) belantamab mafodotin (belamaf) is used to treat relapsed/refractory multiple myeloma (R/R MM) that is refractory to immunomodulatory drugs (IMiD), proteasome inhibitors (PIs), and anti-CD38 mAb therapy, otherwise known as triple-class refractory myeloma. However, belamaf is also associated with frequent ocular adverse events that can cause symptoms such as blurry vision. Its administration requires a multidisciplinary approach that includes oncologists and eye care specialists, to monitor patients for ocular toxicities and adjust drug dosage when necessary. In this educational activity, an expert ophthalmologist and an oncologist review strategies to monitor, grade, and manage ocular toxicities associated with ADCs, and review how to apply collaborative strategies between specialties to best monitor and educate patients.
Acknowledgement of Commercial Support
This activity is supported by an educational grant from GlaxoSmithKline.
Instructions for This Activity and Receiving Credit
You may immediately download your certificate. |
Target Audience
This educational activity is intended for hematologists/oncologists, ophthalmologists, and optometrists.
Learning Objectives
Upon successful completion of this activity, you should be better prepared to:
- Explain the impact of disease-related factors, risk assessment, and treatment history on antibody-based therapy decisions in R/R MM
- Evaluate the clinical profiles of antibody-based therapies in R/R MM
- Implement strategies to monitor, grade, and manage ocular toxicities associated with ADCs
- Apply effective collaborative strategies for the multidisciplinary management of ADC-related ocular toxicities
Faculty, Staff, and Planners’ Disclosures
The staff of Physicians’ Education Resource®, LLC have no relevant financial relationships with ineligible entities.
Faculty
Professor and Chair
Department of Hematology and Medical Oncology
Anne and Bernard Gray Professor in Cancer
Emory University School of Medicine
Chief Medical Officer
Winship Cancer Institute
Emory University
Atlanta, GA
Disclosures: Grant/Research Support: BMS, Celgene, Janssen, Takeda; Consultant: AbbVie, Amgen, BMS, Celgene, GSK, Janssen Sanofi, Novartis, Takeda; Other: TG Therapeutics (Board of Directors).
Associate Ophthalmologist
Northern California Cornea Associates, Inc.
Attending Ophthalmologist/Teaching Faculty
Department of Ophthalmology
Highland Hospital
Oakland, CA
Disclosures: Speaker’s Bureau: GlaxoSmithKline.
PER® mitigated all COI for faculty, staff, and planners prior to the start of this activity by using a multistep process.
Off-Label Disclosure and Disclaimer
This activity may or may not discuss investigational, unapproved, or off-label use of drugs. Learners are advised to consult prescribing information for any products discussed. The information provided in this accredited activity is for continuing education purposes only and is not meant to substitute for the independent clinical judgment of a healthcare professional relative to diagnostic, treatment, or management options for a specific patient’s medical condition. The opinions expressed in the content are solely those of the individual faculty members and do not reflect those of PER® or any company that provided commercial support for this activity.
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