Why the study?
Immune checkpoint inhibitors may cause cardiovascular immune-related adverse events, but whether pre-treatment coronary artery calcium deposition predicts these events is unknown.
Does positive coronary artery calcium on pre-treatment chest CT predict cardiovascular immune-related adverse events in patients treated with immune checkpoint inhibitors?
Does positive coronary artery calcium on pre-treatment chest CT predict cardiovascular immune-related adverse events in patients treated with immune checkpoint inhibitors?
Visual assessment of pre-treatment coronary artery calcium on non-gated chest CT did not independently predict cardiovascular immune-related adverse events or mortality in cancer patients treated with immune checkpoint inhibitors.
Pre-treatment CAC lacks independent predictive value for CV irAEs; leaves open need for validated risk tools in ICI therapy.
BACKGROUND: Immune checkpoint inhibitors (ICIs) have become the standard for treating various cancers. Nevertheless, their use may lead to significant cardiovascular immune-related adverse events (CV irAEs). OBJECTIVES: We aimed to assess whether pre-treatment coronary artery calcium (CAC) deposition predicts CV irAEs in patients treated with ICIs. METHODS: A retrospective single-center cohort of patients treated with ICIs who performed pre-treatment chest computed tomography. A visual CAC assessment was categorized into Positive or Negative calcium deposits. Patients with pre-existing ischemic heart disease were excluded. The primary endpoint was the composite CV irAEs, including myocarditis, acute coronary syndrome, heart failure, and arrhythmias, and the secondary endpoint was all-cause mortality. RESULTS: The cohort included 240 patients with a median age of 67 (IQR 59-73) years and 47% female. The most prevalent type of cancer was lung cancer (36%), and the prominent ICIs was pembrolizumab (54%). Patients with Positive CAC (38%) were predominantly male, with higher rates of cardiovascular comorbidities. The primary outcome occurred in 36 cases (15%) at a median of 94 (IQR 48-338) days from the first ICIs dose. The Positive CAC group observed a non-significant trend toward a higher hazard for CV irAEs (HR 1.66, 95% CI 0.86-3.21, p = 0.13), with no significant difference in all-cause mortality (HR 1.15, 95% CI 0.88-1.51, p = 0.30). CONCLUSION: Pre-treatment CAC deposition did not demonstrate an independent predictive role in assessing the risk of CV irAEs and all-cause mortality in patients treated with ICIs.
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Slieman et al. (2025) studied this question.
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