Ooki Akira, Shinozaki Eiji, Yamaguchi Kensei
Department of Gastroenterological Chemotherapy, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
J Anus Rectum Colon. 2021 Jan 28;5(1):11-24. doi: 10.23922/jarc.2020-064. eCollection 2021.
Despite the recent advances in the systemic treatment of metastatic colorectal cancer (mCRC), prognostic outcomes have remained to be poor. Thus, what is needed is an innovative treatment approach. Immune checkpoint inhibitors (ICIs) targeting programmed death-1 (PD-1) and anti-programmed cell death ligand 1 (PD-L1) have exhibited a durable response and dominated the treatment of various tumor types. However, in mCRC, the clinical benefit is limited in patients with deficient mismatch repair (dMMR)/high levels of microsatellite instability (MSI-H), comprising approximately 5% of mCRC cases, and some do not respond to ICI treatment. Thus, further research is needed to identify predictive biomarkers. The most urgent need is developing effective immunotherapy for patients with proficient mismatch repair (pMMR)/microsatellite stable (MSS) cancer, which comprises 95% of mCRC cases. Tumors with the pMMR/MSS phenotype often exhibit a lower tumor mutation burden and fewer tumor-infiltrating lymphocytes than dMMR/MSI-H, leading to immune tolerance and evasion in the tumor microenvironment. Therefore, a number of investigative studies aimed at overcoming tumor resistance in current immunotherapy approaches are underway. A better understanding on the complexity and diversity of the immune system's functioning within the tumor microenvironment will increase the potential for developing predictive biomarkers and novel therapeutic strategies to potentiate anti-tumor immunity in patients with mCRC. In this review, we summarize the most recent advances in immunotherapy based on the findings of pivotal clinical trials for patients with mCRC, highlighting potent therapeutic approaches and predictive biomarkers.
尽管转移性结直肠癌(mCRC)的系统治疗最近取得了进展,但其预后结果仍然很差。因此,需要一种创新的治疗方法。靶向程序性死亡1(PD-1)和抗程序性细胞死亡配体1(PD-L1)的免疫检查点抑制剂(ICI)已显示出持久的反应,并主导了各种肿瘤类型的治疗。然而,在mCRC中,错配修复缺陷(dMMR)/微卫星高度不稳定(MSI-H)的患者临床获益有限,这类患者约占mCRC病例的5%,而且一些患者对ICI治疗无反应。因此,需要进一步研究以确定预测性生物标志物。最迫切需要的是为错配修复功能正常(pMMR)/微卫星稳定(MSS)的癌症患者开发有效的免疫疗法,这类患者占mCRC病例的95%。与dMMR/MSI-H肿瘤相比,具有pMMR/MSS表型的肿瘤通常表现出较低的肿瘤突变负荷和较少的肿瘤浸润淋巴细胞,导致肿瘤微环境中的免疫耐受和免疫逃逸。因此,目前有许多旨在克服当前免疫治疗方法中肿瘤耐药性的研究正在进行。更好地了解肿瘤微环境中免疫系统功能的复杂性和多样性,将增加开发预测性生物标志物和新治疗策略的潜力,以增强mCRC患者的抗肿瘤免疫力。在这篇综述中,我们根据针对mCRC患者的关键临床试验结果,总结免疫治疗的最新进展,重点介绍有效的治疗方法和预测性生物标志物。