Coronary artery calcification is not associated with survival in advanced gastric and gastroesophageal junction cancer: a secondary analysis of the EXPAND trial.

J Cancer Res Clin OncolNov 3, 2026 (epub)
Clinical ResearchOncology (Medical)Radiology (Diagnostic)Open access

Hans-Jonas Meyer, Tihomir Dermendzhiev, Paul-Philipp Jacobs et al.

✦ AI-curated · Sources linked

In 30 seconds

This secondary analysis of baseline CT images from the phase III EXPAND trial assessed whether coronary artery calcification (CAC) predicted overall survival in 785 patients with unresectable locally advanced or metastatic gastric or gastroesophageal junction cancer. CAC was scored semiquantitatively using the Weston method. In univariable analysis, CAC presence versus absence was not significantly associated with mortality (HR 1.08, 95% CI 0.92-1.26, p = 0.34); analysis of CAC as a continuous score was also not significant. The findings do not support CAC as a relevant prognostic marker in this population receiving first-line chemotherapy.

Key findings

  • 337 patients (42.9%) had no visible coronary artery calcification.
  • CAC presence versus absence was not significantly associated with survival (HR:1.08, 95% CI: 0.92-1.26, p = 0.34).
  • CAC analysed as a continuous score was also not significantly associated with survival (HR: 0.99, 95% CI: 0.96-1.02, p = 0.74).
  • Male patients had higher median CAC scores than female patients (1 versus 0, p < 0.0001).

Why it matters

CAC is visible on routine staging CT, and its prognostic value has been reported in other cancer settings. In this analysis, however, CAC did not identify differences in overall survival among patients with advanced gastric or gastroesophageal junction cancer. This cautions against assuming that a CT finding has the same prognostic meaning across cancer types.

What to keep in mind

This was a secondary analysis of baseline CT images from a trial, rather than a study designed primarily to evaluate CAC. The reported survival associations are univariable; the abstract does not provide adjusted effect estimates.

Source

Published in J Cancer Res Clin Oncol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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