An Immune Cell Signature Is Associated With Disease-Free Survival and Adjuvant Chemosensitivity of Patients With Resectable Gastric Cancer

• Published in: Frontiers in immunology Vol. 11; p. 621623
• Main Authors: Yan, Hongfei, Chen, Yang, Yang, Zichang, Li, Zhi, Che, Xiaofang, Xiao, Jiawen, Liu, Yunpeng, Qu, Xiujuan
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 04.02.2021
• Subjects: adjuvant chemotherapy; Adult; Aged; Aged, 80 and over; B-Lymphocytes - immunology; Biomarkers, Tumor - immunology; CD4-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - immunology; Chemotherapy, Adjuvant - mortality; Databases, Factual; Databases, Genetic; DFS; Disease-Free Survival; Female; gastric cancer; Humans; Immunology; immunoscore; Kaplan-Meier Estimate; Killer Cells, Natural - immunology; Male; Middle Aged; Neoplasm Metastasis; Neoplasm Staging; Prognosis; Proportional Hazards Models; Stomach Neoplasms - drug therapy; Stomach Neoplasms - immunology; Stomach Neoplasms - mortality; Stomach Neoplasms - pathology; DFS; XP; adjuvant chemotherapy; gastric cancer; immunoscore
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2020.621623

Increasing evidence has indicated that current tumor-node-metastasis (TNM) stage alone cannot predict prognosis and adjuvant chemotherapy benefits accurately for stages II and III gastric cancer (GC) patients after surgery. In order to improve the predictive ability of survival and adjuvant chemotherapy benefits of GC patients after surgery, this study aimed to establish an immune signature based on the composition of infiltrating immune cells. Twenty-eight types of immune cell fractions were evaluated based on the expression profiles of GC patients from the Gene Expression Omnibus (GEO) database using single-sample gene set enrichment analysis (ssGSEA). The immunoscore (IS) was constructed using a least absolute shrinkage and selection operator (LASSO) Cox regression model. Through the LASSO model, an IS classifier consisting of eight immune cells was constructed. Significant difference was found between high-IS and low-IS groups in the training cohort in disease-free survival (DFS, P < 0.0001) and overall survival (OS, P < 0.0001). Multivariate analysis showed that the IS classifier was an independent prognostic indicator. Moreover, a combination of IS and TNM stage exhibited better prognostic value than TNM stage alone. Further analysis demonstrated that low-IS patients who had more tumor-infiltrating lymphocytes had better response to adjuvant chemotherapy. More importantly, we found that patients with high-IS were more likely to benefit from a Xeloda plus cisplatin regimen after surgery. Finally, we established two nomograms to screen the stage II and III GC patients who benefitted from adjuvant chemotherapy after surgery. The combination of IS classifier and TNM stage could predict DFS and OS of GC patients. The IS model has been proven as a promising tool that can be used to identify the patients with stages II and III GC who may benefit from adjuvant chemotherapy.