PGY-2 Oncology Pharmacy Resident Miami Cancer Institute Coral Gables, Florida, United States
Poster Abstract:
Background: Immune checkpoint inhibitors (ICIs), a subset of cancer immunotherapy, augments the immune response against cancer cells. With increased activity of the immune system, side effects include autoimmune-like toxicities known as immune-related adverse events (irAEs). The incidence and prevalence of ICI-related toxicity is still being fully elucidated. Due to non-specific presentation of irAEs, the variety of organ systems involved, and inconsistent reporting, it is likely that reported rates underestimate the actual incidence of these events. The purpose of this study is to evaluate the incidence of irAEs in patients who received ICI therapy and to assess time to guideline recommended treatment.
Objective(s): The primary outcome of this study is quantifying the incidence of irAEs in patients receiving ICIs who required treatment at Baptist Hospital of Miami (BHM). Secondary outcomes include measuring time to treatment of irAEs from patient presentation, percentage of patients receiving appropriate therapeutic management by grade of toxicity, hospital length of stay, 30-day hospital readmission rate, and mortality during hospitalization.
Methods: This is a single-center, retrospective chart review of patients at least 18 years of age or older who presented to BHM, received an ICI between March 1, 2022 and June 30, 2023, and were treated for one of the pre-specified subset of ICD-10 codes denoting a potential irAE between July 1, 2022 and June 30, 2023. Patients were excluded if they received an ICI in combination with other oral or parenteral chemotherapy agents (excluding ICI-combination therapies), if they had a history of autoimmune disease prior to receiving an ICI, or if they were pregnant. Descriptive statistics will be utilized to report median, range, and frequency for each respective endpoint.
Results and Discussion/
Conclusions: The results and conclusions/discussion of this study are pending completion
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