Key result
Chemoradiotherapy linked to ~41% greater LV myocardial 18F-FDG uptake, indicating higher cardiovascular risk.
Why the study?
Cardiovascular side-effects of chemoradiotherapy for NSCLC remain a major concern, and insights into vascular changes in atherosclerotic burden and disease activity secondary to chemoradiotherapy are useful to predict cardiovascular risk.
Does chemoradiotherapy increase aortic atherosclerotic burden and cardiovascular inflammation in patients with stage 3B non-small cell lung cancer?
Observational (n=26)
Yes
Does chemoradiotherapy increase aortic atherosclerotic burden and cardiovascular inflammation in patients with stage 3B non-small cell lung cancer?
p-value: p=<0.05
Chemoradiotherapy for advanced NSCLC is associated with increased metabolic activity in the left ventricular myocardium and accelerated calcified aortic plaque burden at 14 weeks, suggesting a mechanism for increased cardiovascular risk.
May warrant closer CV surveillance after chemoradiotherapy in stage 3B NSCLC; leaves open need for prospective validation before practice change.
Background Cardiovascular side-effects of chemoradiotherapy for non-small cell lung cancer (NSCLC) remain a major concern. Insights into vascular changes in atherosclerotic burden and overall disease activity secondary to chemoradiotherapy are useful to predict cardiovascular risk. Computed tomography (CT) calcium score is a biomarker of atherosclerosis while [18F] Fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging can evaluate cardiovascular inflammation. Purpose In patients with advanced NSCLC undergoing repeated [18F] FDG PET/CT imaging, we investigated the effects of chemoradiotherapy on aortic atherosclerotic burden assessed by aortic calcium score, and atherosclerotic disease activity with [18F] FDG uptake. Methods All available oncology PET-CT scans of patients with stage 3B NSCLC from the American College of Radiology Imaging Network (ACRIN 6668) trial were retrieved from the Cancer Imaging Archive and a retrospective analysis was performed. Pre- and post-treatment scans were performed approximately 14 weeks apart. Volumes of interest for the left ventricle, aorta and major non-cardiac organs were manually delineated on all PET-CT scans. Average standard uptake values (SUV), target-to-background ratios (TBR) to aortic blood pool and calcium score were quantified. Aortic PET uptake was analysed for both calcified and non-calcified areas and comparisons before and after treatment scans were performed. Results A total of 26 patients (mean 60±9 years, body-mass index 25±5 kg/m2) met the inclusion criteria. After chemoradiotherapy, calcium score increased by 10% in calcified aortic plaques (p<0.05) (Figure 1A ). [18F]FDG SUVmean uptake was 41% higher in the left ventricular myocardium (p=0.01), but no change was observed in the [18F]FDG uptake of non-cardiac organs (table 1). [18F]FDG TBRmean uptake was 4% higher in calcified aortic plaques (p=0.02), but no change was observed in non-calcified areas of the aorta (Figure 1B,C). Conclusion Metabolic activity is selectively increased in the left ventricular myocardium and calcified aortic atherosclerotic plaques following chemoradiotherapy for NSCLC. Chemoradiotherapy resulted in both an increase in aortic metabolic activity and burden of calcified plaques highlighting an accelerated disease process suggesting an increased cardiovascular risk.
No takes yet. Share an insight, caveat, or question.
Khaing et al. (2026) conducted an observational in Advanced non-small cell lung cancer (n=26). Chemoradiotherapy vs. Pre-treatment baseline was evaluated on Aortic atherosclerotic burden (calcium score) and atherosclerotic disease activity ([18F] FDG uptake) (p=<0.05). Following chemoradiotherapy for NSCLC, calcium score increased by 10% in calcified aortic plaques (p<0.05) and [18F]FDG SUVmean uptake was 41% higher in the left ventricular myocardium (p=0.01).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: