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免疫治疗在转移性和局部晚期胃食管腺癌治疗中的现状与未来展望。

The current status of immunotherapy and future horizon in the treatment of metastatic and locally advanced gastroesophageal adenocarcinoma.

机构信息

Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

出版信息

Expert Opin Biol Ther. 2024 Sep;24(9):903-915. doi: 10.1080/14712598.2024.2395921. Epub 2024 Aug 28.

Abstract

INTRODUCTION

Immunochemotherapy with PD-1 blockade has been established as the current standard first-line therapy for patients with mGEA. Reviewing the history of clinical trials offers valuable insight into the evolution of immune oncology in mGEA, paving the way for future advancements in this field.

AREAS COVERED

This review summarizes the findings of previous clinical trials related to immunotherapy for patients with GEA in the metastatic and locally advanced setting. We also introduce ongoing clinical trials to address the current challenging issues in clinical practice.

EXPERT OPINION

In general, GEA exhibits intermediate immunogenic characteristics with heterogeneous expressions, and responders to anti-PD-(L)1 therapy are mostly enriched to patients with specific genomic profiles such as MSI-H, high PD-L1 expression, high TMB, and EBV-associated type. Co-administration with anti-angiogenic agents or simultaneous blockade of immune checkpoint molecules is being explored to offer benefit of immunotherapy for more patients. We hope that CLDN18.2 and upcoming targets like FGFR2b will complement the treatment niche of immunotherapy in the field of mGEA. Bispecific antibodies, antibody drug conjugates, CAR-T, and vaccine are anticipated to enhance efficacy and expand the scope of immunotherapy.

摘要

简介

免疫化疗联合 PD-1 阻断已成为 mGEA 患者的当前标准一线治疗。回顾临床试验的历史为 mGEA 中的免疫肿瘤学的发展提供了有价值的见解,为该领域的未来进展铺平了道路。

涵盖领域

本综述总结了先前与转移性和局部晚期 GEA 患者免疫治疗相关的临床试验结果。我们还介绍了正在进行的临床试验,以解决当前临床实践中的难题。

专家意见

一般来说,GEA 表现出中等免疫原性特征,表达具有异质性,对抗 PD-(L)1 治疗有反应的患者大多富集于具有特定基因组特征的患者,如 MSI-H、高 PD-L1 表达、高 TMB 和 EBV 相关类型。正在探索与抗血管生成药物联合用药或同时阻断免疫检查点分子,以让更多患者受益于免疫治疗。我们希望 CLDN18.2 和即将出现的 FGFR2b 等靶点将补充免疫治疗在 mGEA 领域的治疗空白。双特异性抗体、抗体药物偶联物、CAR-T 和疫苗有望提高疗效并扩大免疫治疗的范围。

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