免疫系统
结直肠癌
医学
微卫星不稳定性
彭布罗利珠单抗
肿瘤微环境
化疗
免疫检查点
癌症研究
肿瘤科
免疫疗法
黑色素瘤
癌症
内科学
免疫学
生物
等位基因
基因
微卫星
生物化学
作者
Ji Hyung Hong,In Sook Woo
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2023-05-19
卷期号:565: 216236-216236
被引量:11
标识
DOI:10.1016/j.canlet.2023.216236
摘要
The use of immune checkpoint inhibitors (ICIs) in clinical practice for the treatment of metastatic colorectal cancer (mCRC) is currently limited to patients with deficient mismatch repair (dMMR) or high microsatellite instability (MSI-H), which comprise less than 5% of all mCRC cases. Combining ICIs with anti-angiogenic inhibitors, which modulate the tumor microenvironment, may reinforce and synergize the anti-tumor immune responses of ICIs. In mCRCs, combinations of pembrolizumab and lenvatinib have shown good efficacy in early phase trials. These results suggest the potential utility of immune modulators as partners in combination treatment with ICIs in immunologically cold microsatellite stable, as well as hot dMMR/MSI-H tumors. Unlike conventional pulsatile maximum tolerated dose chemotherapy, low-dose metronomic (LDM) chemotherapy recruits immune cells and normalizes vascular-immune crosstalk, similar to anti-angiogenic drugs. LDM chemotherapy mostly modulates the tumor stroma rather than directly killing tumor cells. Here, we review the mechanism of LDM chemotherapy in terms of immune modulation and its potential as a combination partner with ICIs for the treatment of patients with mCRC tumors, most of which are immunologically cold.
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