[Immunotherapy for gastrointestinal cancer].

Pub Date : 2024-04-01 DOI:10.1055/a-2060-2192
Getraud Stocker, Ulrich Hacker, Florian Lordick
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Abstract

Cancers of gastrointestinal tract make up the largest group of solid tumour diseases in Germany. The prognosis at diagnosis is often critical. Drug therapies reduce the risk of relapse after resection and can halt the progression of metastatic disease. Immunotherapies contribute increasingly to the treatment of gastrointestinal tumours. Monoclonal antibodies (mAB) against surface receptors from the epidermal growth factor receptor family (EGFR, Her2) are well established. The effect is partly based on the interruption of the oncogenic downstream signalling cascades and partly on immune effector mechanisms such as antibody-dependent cellular cytotoxicity. In clinical practice mAB directed against programmed cell death protein 1 (PD-1), its ligand (PD-L1) and cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) - so-called immune checkpoint inhibitors - play an increasing role and change the natural history of some subgroups of gastrointestinal cancers, especially those with deficient DNA mismatch repair which leads to genomic microsatellite instability.
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[胃肠癌免疫疗法]。
在德国,胃肠道癌症是最大的实体瘤疾病。确诊时的预后往往至关重要。药物疗法可降低切除术后复发的风险,并能阻止转移性疾病的发展。免疫疗法在胃肠道肿瘤的治疗中发挥着越来越重要的作用。针对表皮生长因子受体家族(表皮生长因子受体、Her2)表面受体的单克隆抗体(mAB)已得到广泛应用。其效果部分基于对致癌下游信号级联的干扰,部分基于免疫效应机制,如抗体依赖性细胞毒性。在临床实践中,针对程序性细胞死亡蛋白 1(PD-1)、其配体(PD-L1)和细胞毒性 T 淋巴细胞相关蛋白-4(CTLA-4)的 mAB--即所谓的免疫检查点抑制剂--发挥着越来越大的作用,并改变了某些亚组胃肠道癌症的自然病史,尤其是那些 DNA 错配修复缺陷导致基因组微卫星不稳定的癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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