Abstract 4365072: Immune checkpoint inhibitor myocarditis presenting as acute coronary syndrome

Case: A 64-year-old male with stage IV squamous cell carcinoma on durvalumab (last dose 2 months prior) presented with acute dyspnea on exertion. Vitals were notable for heart rate of 128 beats per minute and oxygen saturation of 92% on 4 liters of nasal cannula. EKG showed ST elevation in V1-2 and aVR, with reciprocal ST depressions in II, III, and aVF. Labs revealed troponin >10,000 ng/L and BNP 14,492 pg/mL. Computed tomography angiography (CTA) ruled out pulmonary embolism. Transthoracic echocardiogram (TTE) showed left ventricular ejection fraction (EF) 48% with hypokinesis of the left ventricular septum. Emergent coronary angiography demonstrated non-obstructive coronary artery disease. Cardiac MRI revealed mid-myocardial late gadolinium enhancement, and endomyocardial biopsy confirmed CD8+ T-cell infiltration consistent with ICI-induced myocarditis. His hospital course was complicated by an episode of sustained monomorphic ventricular tachycardia, managed with amiodarone, followed by placement of a subcutaneous implantable cardioverter-defibrillator. Treatment with high-dose corticosteroid therapy followed by Abatacept for ICI-induced myocarditis led to resolution of symptoms and improvement in cardiac biomarkers, allowing for the patient to be safely discharged. Discussion: Immune checkpoint inhibitors (ICIs) targeting programmed cell death protein 1 (PD-1) and its ligand PD-L1 have transformed cancer therapy but are associated with rare and potentially fatal immune-related adverse events such as myocarditis. While ICI myocarditis can typically cause non-specific EKG findings and arrhythmias, it is unusual for patients to present with ST-segment elevations and markedly elevated troponins mimicking acute coronary syndrome (ACS) in the absence of obstructive coronary disease. This case emphasizes the importance of considering myocarditis in the differential diagnosis of ACS-like presentations in patients receiving immunotherapy, particularly when angiography is unrevealing. In these cases, Cardiac MRI and endomyocardial biopsy can aid in diagnosis when standard ischemic workups are inconclusive. As the use of ICIs becomes more common, recognition of this presentation is critical for cardiologists as early diagnosis and intervention can prevent life-threatening arrhythmias and improve outcomes in patients receiving immunotherapy.

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Publication Details

Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4365072
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
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article

Abstract 4365072: Immune checkpoint inhibitor myocarditis presenting as acute coronary syndrome

Artemio Zavala, Mina Zheng, Ryan F. Heslin, Matthew H. Pelletier et al.
Circulation
Cancer Immunotherapy and Biomarkers
article

Abstract 4365072: Immune checkpoint inhibitor myocarditis presenting as acute coronary syndrome

Artemio Zavala, Mina Zheng, Ryan F. Heslin, Matthew H. Pelletier, Anupama Sharma, Kenney Abraham
article en

Abstract

Case: A 64-year-old male with stage IV squamous cell carcinoma on durvalumab (last dose 2 months prior) presented with acute dyspnea on exertion. Vitals were notable for heart rate of 128 beats per minute and oxygen saturation of 92% on 4 liters of nasal cannula. EKG showed ST elevation in V1-2 and aVR, with reciprocal ST depressions in II, III, and aVF. Labs revealed troponin >10,000 ng/L and BNP 14,492 pg/mL. Computed tomography angiography (CTA) ruled out pulmonary embolism. Transthoracic echocardiogram (TTE) showed left ventricular ejection fraction (EF) 48% with hypokinesis of the left ventricular septum. Emergent coronary angiography demonstrated non-obstructive coronary artery disease. Cardiac MRI revealed mid-myocardial late gadolinium enhancement, and endomyocardial biopsy confirmed CD8+ T-cell infiltration consistent with ICI-induced myocarditis. His hospital course was complicated by an episode of sustained monomorphic ventricular tachycardia, managed with amiodarone, followed by placement of a subcutaneous implantable cardioverter-defibrillator. Treatment with high-dose corticosteroid therapy followed by Abatacept for ICI-induced myocarditis led to resolution of symptoms and improvement in cardiac biomarkers, allowing for the patient to be safely discharged. Discussion: Immune checkpoint inhibitors (ICIs) targeting programmed cell death protein 1 (PD-1) and its ligand PD-L1 have transformed cancer therapy but are associated with rare and potentially fatal immune-related adverse events such as myocarditis. While ICI myocarditis can typically cause non-specific EKG findings and arrhythmias, it is unusual for patients to present with ST-segment elevations and markedly elevated troponins mimicking acute coronary syndrome (ACS) in the absence of obstructive coronary disease. This case emphasizes the importance of considering myocarditis in the differential diagnosis of ACS-like presentations in patients receiving immunotherapy, particularly when angiography is unrevealing. In these cases, Cardiac MRI and endomyocardial biopsy can aid in diagnosis when standard ischemic workups are inconclusive. As the use of ICIs becomes more common, recognition of this presentation is critical for cardiologists as early diagnosis and intervention can prevent life-threatening arrhythmias and improve outcomes in patients receiving immunotherapy.

CirculationVol. 152(Suppl_3)
Stony Brook University Hospital (US)
Openalex Percentile: Top 57%
Cancer Immunotherapy and Biomarkers
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