4.6 Article

Application of Circulating Tumor Cells and Interleukin-6 in Preoperative Prediction of Peritoneal Metastasis of Advanced Gastric Cancer

Journal

JOURNAL OF INFLAMMATION RESEARCH
Volume 16, Issue -, Pages 3033-3047

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S414786

Keywords

circulating tumor cell counts; interleukin-6; advanced gastric cancer; peritoneal metastasis; occult peritoneal metastasis

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This study aimed to explore the clinical significance of circulating tumor cells (CTCs) and cytokines in predicting peritoneal metastasis (PM) in advanced gastric cancer (AGC) patients preoperatively. The levels of CTCs and interleukin-6 (IL-6) were found to be higher in AGC patients with PM compared to those without PM. Multivariate logistic regression analysis identified IL-6 > 12.22 pg/mL, CTCs > 4/5mL, CA724 > 6 IU/mL, CA125 > 35 U/mL, and tumor size > 5 cm as independent risk factors for PM in AGC. The nomogram constructed from these risk factors demonstrated good discriminative ability and clinical utility.
Background: The purpose of this study was to explore the clinical significance of circulating tumor cells (CTCs) and cytokines in peripheral blood in preoperative prediction of peritoneal metastasis (PM) in advanced gastric cancer (AGC). Methods: The clinicopathological characteristics of 282 patients with AGC were retrospectively analyzed. The patients were divided into training and validation groups according to the time of receiving treatment. We used univariate analysis and multivariate logistic regression analysis to screen out the independent risk factors of PM in AGC. Then, we incorporated independent risk factors into the nomogram, and evaluated the discriminative ability. Results: The levels of CTCs and interleukin-6 (IL-6) of AGC patients with PM were higher than those without PM (P<0.05). Moreover, the levels of CTCs and IL-6 in the occult peritoneal metastasis (OPM) group and the CT-positive PM group were higher than those in the negative PM (P<0.05). Multivariate logistic regression analysis showed that IL-6 > 12.22 pg/mL, CTCs > 4/5mL, CA724 > 6 IU/mL, CA125 > 35 U/mL and tumor size > 5 cm were independent risk factors for PM of AGC. The area under the ROC curve of the nomogram were 0.898 and 0.926 in the training and validation sets, respectively. The clinical decision curve showed that the nomogram had good clinical utility. Conclusion: CTCs and IL-6 in peripheral blood are promising biomarkers for predicting the risk of PM in AGC. The nomogram constructed from five risk factors can effectively assess the risk of PM in AGC patients individually.

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