Recent Advances in Combination of Immunotherapy and Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma

被引:30
|
作者
Wang, Ruixi [1 ,2 ]
Liu, Shiliang [1 ,2 ]
Chen, Baoqing [1 ,2 ]
Xi, Mian [1 ,2 ]
机构
[1] Collaborat Innovat Ctr Canc Med, Guangdong Esophageal Canc Inst, State Key Lab Oncol South China, Guangzhou 510060, Peoples R China
[2] Sun Yat Sen Univ Canc Ctr, Dept Radiat Oncol, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
基金
美国国家卫生研究院;
关键词
esophageal squamous cell carcinoma; immune checkpoint inhibitors; immunotherapy; chemoradiotherapy; locally advanced; CHEMOTHERAPY; NIVOLUMAB; SURVIVAL; THERAPY; PLACEBO;
D O I
10.3390/cancers14205168
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Neoadjuvant chemoradiotherapy (CRT), followed by surgery or definitive CRT, is the standard treatment for locally advanced esophageal squamous cell carcinoma (ESCC); however, the clinical outcomes remain unsatisfactory. Immunotherapy combined with CRT is currently being investigated as a novel treatment option for locally advanced ESCC. In this review, we discuss the theoretical background and status of immunotherapy for locally advanced ESCC and potential biomarkers for predicting tumor response and prognosis. Esophageal cancer has a high mortality rate and a poor prognosis, with more than one-third of patients receiving a diagnosis of locally advanced cancer. Esophageal squamous cell carcinoma (ESCC) is the dominant histological subtype of esophageal cancer in Asia and Eastern Europe. Although neoadjuvant or definitive chemoradiotherapy (CRT) has been the standard treatment for locally advanced ESCC, patient outcomes remain unsatisfactory, with recurrence rates as high as 30-50%. The combination of immune checkpoint inhibitors (ICIs) and CRT has emerged as a novel strategy to treat esophageal cancer, and it may have a synergistic action and provide greater efficacy. In the phase III CheckMate-577 trial, one year of adjuvant nivolumab after neoadjuvant CRT improved disease-free survival in patients with residual disease on pathology. Moreover, several phase I and II studies have shown that ICIs combined with concurrent CRT may increase the rate of pathologic complete response for resectable ESCC, but they lack long-term follow-up results. In unresectable cases, the combination of camrelizumab and definitive CRT showed promising results against ESCC in a phase Ib trial. Phase III randomized trials are currently ongoing to investigate the survival benefits of ICIs combined with neoadjuvant or definitive CRT, and they will clarify the role of immunotherapy in locally advanced ESCC. Additionally, valid biomarkers to predict tumor response and survival outcomes need to be further explored.
引用
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页数:11
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