微卫星不稳定性
无容量
彭布罗利珠单抗
DNA错配修复
结直肠癌
医学
癌症研究
免疫系统
免疫检查点
肿瘤科
免疫疗法
内科学
癌症
免疫学
生物
遗传学
基因
等位基因
微卫星
作者
Daniel Almquist,Daniel H. Ahn,Tanios Bekaii‐Saab
出处
期刊:BioDrugs
[Adis, Springer Healthcare]
日期:2020-04-03
卷期号:34 (3): 349-362
被引量:49
标识
DOI:10.1007/s40259-020-00420-3
摘要
Over the past decade, immune checkpoint inhibitors (ICI) have proven to be promising agents in a number of solid tumor malignancies. Pembrolizumab and nivolumab are ICIs that target programmed cell death protein 1 and both have been approved by the US Food and Drug Administration for the treatment of microsatellite instability-high/DNA mismatch repair deficient (MSI-H/dMMR) colorectal cancer (CRC). In MSI-H/dMMR CRC, these agents were found to have considerable antitumor activity and are now used in the treatment of this disease. However, MSI-H/dMMR tumors account for only 5% of metastatic CRC and the remaining patients are identified as being microsatellite stable/DNA mismatch repair proficient (MSS/pMMR). In MSS/pMMR CRC, ICIs were found to have no antitumor activity and they are not currently used in the treatment of the disease. However, ongoing research is expanding our knowledge of how the human immune system interacts with cancer cells. Identifying mechanisms to improve our immune response to MSS/pMMR CRC is of utmost importance. In this review, we discuss available clinical data and the emerging role of immune-based strategies to overcome the resistance to ICI therapy in the treatment of MSS/pMMR CRC.
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