Key result
Calcified and inflamed carotid plaques on [⁶⁸Ga]DOTA-TOC PET/CT linked to ~15% stroke and increased MACE.
Why the study?
Carotid atherosclerosis features inflammation and calcification at different stages, and simultaneous assessment of both features may improve risk stratification for stroke and MACE.
Does combined assessment of carotid plaque inflammation and calcification on [⁶⁸Ga]DOTA-TOC PET/CT predict stroke and MACE in patients with suspected or confirmed neuroendocrine tumors?
Cohort (n=353)
Does combined assessment of carotid plaque inflammation and calcification on [⁶⁸Ga]DOTA-TOC PET/CT predict stroke and MACE in patients with suspected or confirmed neuroendocrine tumors?
p-value: p=<0.05
Simultaneous assessment of carotid plaque inflammation and calcification on [⁶⁸Ga]DOTA-TOC PET/CT identifies patients at particularly high risk of stroke and MACE.
May identify high-risk patients via combined plaque imaging but should not change practice; leaves open targeted intervention trials.
PURPOSE: Carotid atherosclerosis is a risk factor for stroke and major adverse cardiovascular events (MACE) and is characterized by inflammation and calcification at different stages. Simultaneous assessment of both features may improve risk stratification. We therefore evaluated whether combined assessment of carotid plaque inflammation and calcification on [⁶⁸Ga]DOTA-TOC PET/CT predicts stroke and MACE in a real-world oncologic population. METHODS: We retrospectively included patients who underwent [⁶⁸Ga]DOTA-TOC PET/CT for suspected or confirmed neuroendocrine tumors. Carotid plaques were assessed visually and semiquantitatively on PET/CT, and patients were categorized into four groups according to the patient-level presence of carotid artery calcification and/or focal [⁶⁸Ga]DOTA-TOC uptake. Median follow-up was 55 months (IQR 42-72). Stroke and MACE, defined as myocardial infarction, hospitalization for myocardial ischemia, coronary revascularization, and cardiac death, were recorded. RESULTS: A total of 353 patients were evaluated. Carotid artery calcification was present in 123/353 (34.8%) patients, with a median calcification volume of 77.7 cm³ (IQR 27.9-169.8). Forty-six patients (13.0%) showed 67 foci of [⁶⁸Ga]DOTA-TOC uptake, with median SUVmax 1.68 (IQR 1.55-1.93) and median TBR 2.14 (IQR 1.65-2.79). Patients with both calcified and inflamed carotid plaques had the highest rates of stroke (15.2%) and MACE (12.1%) versus all other groups (P<0.05). In multivariable Cox analysis, this combined patient-level phenotype remained independently associated with stroke and MACE and remained significant in competing-risk analyses. CONCLUSIONS: [⁶⁸Ga]DOTA-TOC PET/CT enables simultaneous assessment of macrophage-related carotid plaque inflammation and calcification and identifies a subgroup at particularly high risk of stroke and MACE.
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Shao et al. (2026) conducted a cohort in Suspected or confirmed neuroendocrine tumors (n=353). [⁶⁸Ga]DOTA-TOC PET/CT vs. Patients without combined calcified and inflamed plaques was evaluated on Stroke and MACE (myocardial infarction, hospitalization for myocardial ischemia, coronary revascularization, and cardiac death) (p=<0.05). Combined calcified and inflamed carotid plaques on [⁶⁸Ga]DOTA-TOC PET/CT were associated with the highest rates of stroke (15.2%) and MACE (12.1%) versus all other groups (P<0.05).
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