Association between radiomics features of DCE-MRI and CD8+ and CD4+ TILs in advanced gastric cancer.

Abstract

Objective: The aim of this investigation was to explore the correlation between the levels of tumor-infiltrating CD8⁺ and CD4⁺ T cells and the quantitative pharmacokinetic parameters of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) in patients with advanced gastric cancer. Methods: We retrospectively analyzed the data of 103 patients with histopathologically confirmed advanced gastric cancer (AGC). Three pharmacokinetic parameters, K_ep, K^trans, and V_e, and their radiomics characteristics were obtained by Omni Kinetics software. Immunohistochemical staining was used to determine CD4⁺ and CD8⁺ TILs. Statistical analysis was subsequently performed to assess the correlation between radiomics characteristics and CD4⁺ and CD8⁺ TIL density. Results: All patients included in this study were finally divided into either a CD8⁺ TILs low-density group (n = 51) (CD8⁺ TILs < 138) or a high-density group (n = 52) (CD8⁺ TILs ≥ 138), and a CD4⁺ TILs low-density group (n = 51) (CD4⁺ TILs < 87) or a high-density group (n = 52) (CD4⁺ TILs ≥ 87). ClusterShade and Skewness based on K_ep and Skewness based on K^trans both showed moderate negative correlation with CD8⁺ TIL levels (r = 0.630-0.349, p < 0.001), with ClusterShade based on K_ep having the highest negative correlation (r = -0.630, p < 0.001). Inertia-based K_ep showed a moderate positive correlation with the CD4⁺ TIL level (r = 0.549, p < 0.001), and the Correlation based on K_ep showed a moderate negative correlation with the CD4⁺ TIL level, which also had the highest correlation coefficient (r = -0.616, p < 0.001). The diagnostic efficacy of the above features was assessed by ROC curves. For CD8⁺ TILs, ClusterShade of K_ep had the highest mean area under the curve (AUC) (0.863). For CD4⁺ TILs, the Correlation of K_ep had the highest mean AUC (0.856). Conclusion: The radiomics features of DCE-MRI are associated with the expression of tumor-infiltrating CD8⁺ and CD4⁺ T cells in AGC, which have the potential to noninvasively evaluate the expression of CD8⁺ and CD4⁺ TILs in AGC patients.