Document Type
Article
Publication Date
10-5-2024
Abstract
BACKGROUND: Immune checkpoint inhibitor (ICI)-mediated myocarditis results in significant morbidity and mortality. At our institution, we noted an increased incidence of ICI-mediated myocarditis cases, leading to further investigation in our database of advanced melanoma patients treated with ICI therapy.
METHODS: A single-center, retrospective cohort analysis of patients with advanced melanoma identified cases of ICI-mediated myocarditis and myositis.
RESULTS: 366 patients with advanced melanoma received a dose of ICI from September 2014 to October 2019. Of these patients, there were 0 cases of ICI-mediated myocarditis (0%, 95% CI 0%-1.0%) and 2 cases of ICI-mediated myositis (0.55%, 95% CI 0.07%-1.96%). From November 2019 to December 2021, an additional 246 patients with advanced melanoma were identified. Of these patients, 10 (4.1%, 95% CI 1.97%-7.35%) developed ICI-mediated myocarditis and 10 developed ICI-mediated myositis.
CONCLUSION: Our study suggests an increase in prevalence of ICI-mediated muscle damage including myositis and myocarditis in the COVID-19 era. Differentiation of these patients and further risk stratification may allow for development of guidelines for nuanced management of this serious complication.
Recommended Citation
Gradone, Allison L.; Ma, Vincent T; Vasbinder, Alexi; Fecher, Leslie A; Yentz, Sarah; Hayek, Salim S; and Lao, Christopher D, "Increased Myositis and Possible Myocarditis in Melanoma Patients Treated with Immune Checkpoint Inhibitors in the COVID-19 Era" (2024). Department of Medical Oncology Faculty Papers. Paper 278.
https://jdc.jefferson.edu/medoncfp/278
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
Language
English
Comments
This article is the author's final published version in Cancer Immunology, Immunotherapy, Volume 73, Issue 12, December 2024, Article number 259.
The published version is available at https://doi.org/10.1007/s00262-024-03803-5.
Copyright © 2024 The Author(s).