Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Tianjin Key Laboratory of Technologies Enabling Development of Clinical Therapeutics and Diagnostics, School of Pharmacy, Tianjin Medical University, Tianjin, China.
Front Immunol. 2024 Sep 30;15:1420399. doi: 10.3389/fimmu.2024.1420399. eCollection 2024.
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.
食管癌(EC)是一种常见的恶性肿瘤,在全球癌症相关死亡率中排名第六。由于大多数 EC 患者在晚期或转移性阶段被诊断出来,手术、化疗和放疗等常规治疗方法的疗效有限,导致 5 年总生存率较差。近年来,免疫检查点抑制剂(ICI)的应用为 EC 患者提供了一种新的治疗途径。ICI 单药治疗以及免疫疗法联合化疗或放化疗(CRT)在晚期 EC 患者中均显示出显著的益处。辅助或新辅助治疗中加入免疫疗法在围手术期治疗中也具有广阔的前景。然而,由于免疫治疗患者的反应存在差异,确定用于患者分层的预测生物标志物对于确定可能从免疫治疗中获益更大的亚组至关重要。在这篇综述中,我们从三个方面总结了 EC 中免疫治疗的已验证或潜在的生物标志物:肿瘤细胞相关标志物、肿瘤免疫微环境(TIME)相关因素和宿主相关标志物,为 EC 患者的个体化治疗提供理论依据。