Department of Colorectal Surgery, Shaoxing People's Hospital, The First Affiliated Hospital of Shaoxing University, Shaoxing, Zhejiang Province 312000, PR China.
Department of Medical Oncology, Shaoxing People's Hospital, The First Affiliated Hospital of Shaoxing University, Shaoxing, Zhejiang Province 312000, PR China.
Int Immunopharmacol. 2021 Dec;101(Pt B):108337. doi: 10.1016/j.intimp.2021.108337. Epub 2021 Nov 11.
Immunotherapy has growingly been prosperous as a promising therapeutic option for several kinds of solid tumors, such as colorectal cancer (CRC), subsequent to initial successful outcomes in the treatment of melanoma. The use of immunotherapy, like nivolumab and pembrolizumab (which are monoclonal antibodies against programmed cell death 1) has shown prosperous outcomes in a group of CRC patients who represent mismatch-repair-deficient and microsatellite instability-high (dMMR-MSI-H). However, a successful outcome of treatment by immune checkpoint inhibitors (ICIs) has not been observed in all of the metastatic CRC patients with dMMR-MSI-H tumors. ICIs are able to block the co-inhibitory signaling transduced in T cells, resulting in increased cytotoxic activity of T cells and efficient killing of tumor cells. In spite of availability of diverse immunotherapeutics in treatment of advanced CRC, a poor survival rate of such approaches has been reported along with challenges in the clinical practice. It is necessary to identify novel biomarkers and molecular signatures to approximate the outcome of ICI therapy in the metastatic CRC patients with dMMR-MSI-H tumors. Here we tried to clarify the current line of evidence regarding immunotherapeutics in the treatment of CRC, and discuss the challenges and hurdles in the management of these patients.
免疫疗法在治疗多种实体肿瘤方面越来越受到关注,如结直肠癌(CRC),继黑色素瘤治疗取得初步成功后。免疫疗法的应用,如nivolumab 和 pembrolizumab(针对程序性细胞死亡 1 的单克隆抗体),在一组代表错配修复缺陷和微卫星不稳定高(dMMR-MSI-H)的 CRC 患者中显示出了良好的疗效。然而,并非所有 dMMR-MSI-H 肿瘤的转移性 CRC 患者都能通过免疫检查点抑制剂(ICIs)治疗获得成功。ICIs 能够阻断 T 细胞中传递的共抑制信号,从而增加 T 细胞的细胞毒性活性并有效杀死肿瘤细胞。尽管在治疗晚期 CRC 方面有多种免疫疗法可用,但据报道,这些方法的生存率仍然很低,并且在临床实践中也存在挑战。有必要确定新的生物标志物和分子特征,以预测 dMMR-MSI-H 肿瘤的转移性 CRC 患者接受 ICI 治疗的效果。在这里,我们试图阐明目前关于 CRC 治疗的免疫治疗证据,并讨论管理这些患者所面临的挑战和障碍。