Emory University School of Medicine, Winship Cancer Institute, Atlanta, USA.
Br J Cancer. 2019 Nov;121(10):809-818. doi: 10.1038/s41416-019-0599-y. Epub 2019 Oct 14.
Metastatic colorectal cancer (CRC) with a mismatch repair-deficiency (MMR-D)/microsatellite instability-high (MSI-H) phenotype carries unique characteristics such as increased tumour mutational burden and tumour-infiltrating lymphocytes. Studies have shown a sustained clinical response to immune checkpoint inhibitors with dramatic clinical improvement in patients with MSI-H/MMR-D CRC. However, the observed response rates range between 30% and 50% suggesting the existence of intrinsic resistance mechanisms. Moreover, disease progression after an initial positive response to immune checkpoint inhibitor treatment points to acquired resistance mechanisms. In this review article, we discuss the clinical trials that established the efficacy of immune checkpoint inhibitors in patients with MSI-H/MMR-D CRC, consider biomarkers of the immune response and elaborate on potential mechanisms related to intrinsic and acquired resistance. We also provide a perspective on possible future therapeutic approaches that might improve clinical outcomes, particularly in patients with actionable resistance mechanisms.
微卫星不稳定高(MSI-H)/错配修复缺陷(MMR-D)型转移性结直肠癌(CRC)具有独特的特征,如肿瘤突变负担增加和肿瘤浸润淋巴细胞增多。研究表明,免疫检查点抑制剂对 MSI-H/MMR-D CRC 患者具有持续的临床反应,显著改善了患者的临床状况。然而,观察到的应答率在 30%至 50%之间,这表明存在内在的耐药机制。此外,在免疫检查点抑制剂治疗初始阳性反应后疾病进展表明存在获得性耐药机制。在这篇综述文章中,我们讨论了确定免疫检查点抑制剂在 MSI-H/MMR-D CRC 患者中的疗效的临床试验,考虑了免疫反应的生物标志物,并详细阐述了与内在和获得性耐药相关的潜在机制。我们还对可能改善临床结局的潜在治疗方法提供了展望,特别是针对具有可操作耐药机制的患者。