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胃癌的免疫治疗。

Immunotherapy in Gastric Cancer.

机构信息

Campus Virchow-Klinikum, Medizinische Klinik m.S. Hämatologie, Onkologie und Tumorimmunologie, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Augustenburger Platz 1, 13353 Berlin, Germany.

Universitätsmedizin der Johannes Gutenberg-Universität Mainz, 55131 Mainz, Germany.

出版信息

Curr Oncol. 2022 Mar 2;29(3):1559-1574. doi: 10.3390/curroncol29030131.

Abstract

Immune checkpoint inhibition is a new standard of targeted therapy in the treatment of advanced or metastatic gastric cancer (GC) and is represented in various combinations with and without chemotherapy in every therapy line within clinical trials. In advanced adenocarcinoma of GC, gastroesophageal junction cancer (GEJC) and esophageal cancer (EC), the combination of nivolumab and chemotherapy in first-line therapy improves overall survival (OS) in PD-L1 (programmed cell death protein 1)-positive patients with approval in Europe (PD-L1 CPS (combined positivity score) ≥ 5), USA and Taiwan (CHECKMATE-649) and pembrolizumab plus chemotherapy for GEJC and EC in Europe (CPS ≥ 10) and the USA (KEYNOTE-590). Furthermore, pembrolizumab plus trastuzumab and chemotherapy show clear benefits in OS and are approved as first-line treatment of Her2 (human epidermal growth factor receptor-2)-positive tumors in the USA (KEYNOTE-811). Nivolumab demonstrates superior OS regardless of PD-L1 expression in third-line therapy with approval in Japan (ATTRACTION-02) and pembrolizumab prolonged the duration of response in PD-L1 positive patients with approval in the USA in PD-L1 CPS ≥ 1 patients (KEYNOTE-059). This review reflects the rationale and current results of phase II and III clinical trials investigating various immune checkpoint inhibitors targeting PD-L1/1 and CTLA (anticytotoxic T-lymphocyte-associated antigen)-4 in combination with and without chemotherapy and Her2-targeted therapy in GC.

摘要

免疫检查点抑制是治疗晚期或转移性胃癌(GC)的一种新的靶向治疗标准,在临床试验的每一条治疗线上,都有与化疗联合或不联合的各种组合。在 GC 的晚期腺癌、胃食管交界处癌(GEJC)和食管癌(EC)中,nivolumab 与化疗联合作为一线治疗,在 PD-L1(程序性死亡蛋白 1)阳性的患者中提高了总生存期(OS),在欧洲(PD-L1 CPS(联合阳性评分)≥5)、美国和中国台湾(CHECKMATE-649)获得批准,pembrolizumab 联合化疗用于 GEJC 和 EC,在欧洲(CPS≥10)和美国(KEYNOTE-590)获得批准。此外,pembrolizumab 联合曲妥珠单抗和化疗在 OS 方面有明显获益,在美国被批准用于 Her2(人表皮生长因子受体-2)阳性肿瘤的一线治疗(KEYNOTE-811)。nivolumab 在日本(ATTRACTION-02)的三线治疗中,无论 PD-L1 表达情况如何,均显示出优越的 OS,pembrolizumab 在 PD-L1 CPS≥1的患者中延长了反应持续时间,在美国获得批准(KEYNOTE-059)。这篇综述反映了针对 PD-L1/1 和 CTLA(细胞毒性 T 淋巴细胞相关抗原)-4 的各种免疫检查点抑制剂在与化疗和 Her2 靶向治疗联合或不联合的情况下,在 II 期和 III 期临床试验中的原理和当前结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4405/8946975/03de5a1c74ce/curroncol-29-00131-g001.jpg

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