Abstract 4369970: Predictive Value of Coronary Artery Calcification on the baseline PET/CT or Chest CT for MACE and Mortality in Lung Cancer

M MARIA F. GOMEZ ARDILA (Mayo Clinic, Rochester, Rochester, Minnesota, United States) E Eduardo Brenner Muslera (Mayo Clinic, Rochester, Rochester, Minnesota, United States) M Maria Jose Perez Nuques (Mayo Clinic, Rochester, Rochester, Minnesota, United States) E Eduardo Villa Pallares (Mayo Clinic, Rochester, Rochester, Minnesota, United States) E Eduardo Tellez Garcia (Mayo Clinic, Rochester, Rochester, Minnesota, United States) H Hector Cajigas (Mayo Clinic, Rochester, Minnesota, United States) T Thomas Foley (MAYO CLINIC, Rochester, Minnesota, United States) H Hector Villarraga (Mayo Clinic, Rochester, Rochester, Minnesota, United States)

Abstract

Background: Lung cancer is classified into small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC – including adenocarcinoma, squamous cell, and large cell carcinoma). The incidence of major adverse cardiovascular events (MACE)—defined as acute myocardial infarction, acute coronary syndrome/ischemic heart disease requiring revascularization, stroke, and cardiovascular death—have not been well defined in lung cancer patients following treatment. Coronary artery calcifications (CAC) and aortic calcifications (CA) are known cardiovascular risk markers in non-cancer populations. Purpose: To determine whether the presence of CAC or CA, as identified on baseline PET-CT (Positron Emission Tomography–Computed Tomography) or chest CT imaging, is predictive of MACE and all-cause mortality (ACM) in patients with lung cancer. Methods: We conducted a retrospective cohort study of patients diagnosed with SCLC or NSCLC who received chemotherapy, between January 1, 2010, and December 31, 2024. The baseline PET-CT or chest CT scans were reviewed for the presence of CAC and/or CA. Patients were excluded if they lacked baseline imaging or had experienced a MACE before treatment. Univariate and multivariate adjusted Cox regression models were employed to assess associations between CAC/CA and MACE or ACM. The Kaplan-Meier survival analyses was performed to evaluate event-free survival. Results: A total of 385 patients were included (mean age: 74 years, IQR: 67–79), predominantly female (158 [55%]) and white (279 [96.2%]). NSCLC was found in 255 (88%) and SCLC in 35 (12%). CAC was identified in 172 (60%) and CA in 87 (30%). Among patients with NSCLC, the presence of CAC was significantly associated with MACE (HR: 2.84 [95% CI: 1.6–4.8], p=0.0001) (Fig. a), particularly in those with adenocarcinoma (Fig. b). In SCLC, (HR: 1.56 [95% CI: 0.1–14.0], p=ns). On multivariable analysis, CAC remained the strongest predictor of MACE after adjusting for age, hypertension, diabetes, dyslipidemia, and smoking status (HR: 2.6 [95% CI: 1.5–4.4], p=0.0008) (Fig. d). No significant association was found between CA and MACE in either group (p>0.05). ACM was similar for SCLC, squamous cell, and NSCLC (Fig. c). Conclusion: In patients with NSCLC especially lung adenocarcinoma, the presence of CAC in the baseline PET/CT was an independent predictor of MACE. This finding supports the value of CAC as a non-invasive cardiovascular risk marker.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (8)

M

MARIA F. GOMEZ ARDILA

Mayo Clinic, Rochester, Rochester, Minnesota, United States

E

Eduardo Brenner Muslera

Mayo Clinic, Rochester, Rochester, Minnesota, United States

M

Maria Jose Perez Nuques

Mayo Clinic, Rochester, Rochester, Minnesota, United States

E

Eduardo Villa Pallares

Mayo Clinic, Rochester, Rochester, Minnesota, United States

E

Eduardo Tellez Garcia

Mayo Clinic, Rochester, Rochester, Minnesota, United States

H

Hector Cajigas

Mayo Clinic, Rochester, Minnesota, United States

T

Thomas Foley

MAYO CLINIC, Rochester, Minnesota, United States

H

Hector Villarraga

Mayo Clinic, Rochester, Rochester, Minnesota, United States