彭布罗利珠单抗
免疫疗法
微卫星不稳定性
DNA错配修复
医学
临床试验
癌症
癌症免疫疗法
免疫检查点
肿瘤科
生物标志物
癌症研究
免疫学
内科学
结直肠癌
生物
等位基因
生物化学
微卫星
基因
作者
Keitaro Shimozaki,Izuma Nakayama,Toru Hirota,Kensei Yamaguchi
出处
期刊:Cells
[MDPI AG]
日期:2023-03-30
卷期号:12 (7): 1049-1049
被引量:4
标识
DOI:10.3390/cells12071049
摘要
Since pembrolizumab, an anti-programmed death-1 (PD-1) antibody, showed a dramatic response to immunogenic cancers with microsatellite instability-high (MSI-H) and/or deficient mismatch repair (dMMR) in the pilot clinical trial KEYNOTE-016, subsequent studies have confirmed durable responses of anti-PD-1 inhibitors for MSI-H/dMMR solid tumors. As immunotherapy is described as a “game changer,” the therapeutic landscape for MSI-H/dMMR solid tumors including gastrointestinal cancers has changed considerably in the last decade. An MSI/MMR status has been established as the predictive biomarker for immune checkpoint blockades, playing an indispensable role in the clinical practice of patients with MSI-H/dMMR tumors. Immunotherapy is also now investigated for locally advanced MSI-H/dMMR gastrointestinal cancers. Despite this great success, a few populations with MSI-H/dMMR gastrointestinal cancers do not respond to immunotherapy, possibly due to the existence of intrinsic or acquired resistance mechanisms. Clarifying the underlying mechanisms of resistance remains a future task, whereas attempts to overcome resistance and improve the efficacy of immunotherapy are currently ongoing. Herein, we review recent clinical trials with special attention to MSI-H/dMMR gastrointestinal cancers together with basic/translational findings, which provide their rationale, and discuss perspectives for the further therapeutic development of treatment in this field.
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