Prognostic biomarkers for immunotherapy in esophageal cancer

被引:1
作者
Tong, Xu [2 ]
Jin, Meiyuan [2 ]
Wang, Lulu [3 ]
Zhang, Dongli [3 ]
Yin, Yuping [1 ]
Shen, Qian [4 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Gastrointestinal Surg, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan, Peoples R China
[3] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therapeu, Tianjin, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Oncol, Wuhan, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
中国国家自然科学基金;
关键词
esophageal cancer; immunotherapy; biomarkers; ICIs; TIME; SQUAMOUS-CELL CARCINOMA; IMMUNE CHECKPOINT INHIBITORS; POOR-PROGNOSIS; FDA APPROVAL; EXPRESSION; CHEMOTHERAPY; PREDICTS; THERAPY; PEMBROLIZUMAB; MACROPHAGES;
D O I
10.3389/fimmu.2024.1420399
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Esophageal cancer (EC), a common type of malignant tumor, ranks as the sixth highest contributor to cancer-related mortality worldwide. Due to the condition that most patients with EC are diagnosed at advanced or metastatic status, the efficacy of conventional treatments including surgery, chemotherapy and radiotherapy is limited, resulting in a dismal 5-year overall survival rate. In recent years, the application of immune checkpoint inhibitors (ICIs) has presented a novel therapeutic avenue for EC patients. Both ICIs monotherapy and immunotherapy combined with chemotherapy or chemoradiotherapy (CRT) have demonstrated marked benefits for patients with advanced EC. Adjuvant or neoadjuvant therapy incorporating immunotherapy has also demonstrated promising prospects in the context of perioperative treatment. Nonetheless, due to the variable response observed among patients undergoing immunotherapy, it is of vital importance to identify predictive biomarkers for patient stratification, to facilitate identification of subgroups who may derive greater benefits from immunotherapy. In this review, we summarize validated or potential biomarkers for immunotherapy in EC in three dimensions: tumor-cell-associated biomarkers, tumor-immune microenvironment (TIME)-associated factors, and host-associated biomarkers, so as to provide a theoretical foundation to inform tailored therapy for individuals diagnosed with EC.
引用
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页数:18
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