# Case Report: Immune checkpoint inhibitor-associated myocarditis in an esophageal cancer patient with myasthenia gravis following combined radiotherapy and immunotherapy

**Authors:** Xue Ren, Defu Yang, Ying Xu, Ying Yan

PMC · DOI: 10.3389/fonc.2025.1652084 · Frontiers in Oncology · 2026-01-02

## TL;DR

A 69-year-old esophageal cancer patient with myasthenia gravis developed severe myocarditis after receiving combined radiotherapy and immunotherapy, highlighting the risks of this treatment approach.

## Contribution

This case report highlights the rare but severe risk of myocarditis in esophageal cancer patients with myasthenia gravis undergoing combined radiotherapy and immunotherapy.

## Key findings

- The patient exhibited elevated troponin and N-terminal pro-B-type natriuretic peptide levels, indicating cardiac damage.
- Electrocardiography showed arrhythmia and complete left bundle branch block.
- Despite treatment, the patient's condition worsened, leading to death, underscoring the severity of ICI-related myocarditis.

## Abstract

Myocarditis associated with immune checkpoint inhibitors is a rare but potentially fatal immune-related adverse event. Esophageal cancer patients with myasthenia gravis, who are recommended to receive radiotherapy combined with immunotherapy, are at risk for ICI-related myocarditis. We report a 69-year-old male esophageal cancer patient with myasthenia gravis who was diagnosed with immune checkpoint inhibitor related myocarditis after receiving radiotherapy combined with immunotherapy. The patient’s laboratory test results showed elevated troponin and N-terminal pro-B-type natriuretic peptide. Electrocardiography revealed arrhythmia and complete left bundle branch block. Despite treatment with methylprednisolone, the patient’s condition was severe, and clinical and auxiliary examination symptoms continued to deteriorate, leading to his unfortunate demise. In this case, the adverse event of myocarditis induced by radiotherapy combined with immunotherapy in oncology patients with myasthenia gravis is an area that requires further investigation. Clinicians must carefully weigh the potential benefits and risks when considering this combined treatment approach and closely monitor patients for adverse events.

## Linked entities

- **Chemicals:** methylprednisolone (PubChem CID 6741)
- **Diseases:** myocarditis (MONDO:0004496), esophageal cancer (MONDO:0007576), myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Diseases:** Myocarditis (MESH:D009205), myasthenia gravis (MESH:D009157), Esophageal cancer (MESH:D004938), left bundle branch block (MESH:D002037), arrhythmia (MESH:D001145)
- **Chemicals:** Immune (-), methylprednisolone (MESH:D008775)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12807937/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12807937/full.md

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Source: https://tomesphere.com/paper/PMC12807937