Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland.
Cancer Research Institute, New York, New York.
Cancer Immunol Res. 2017 Nov;5(11):942-949. doi: 10.1158/2326-6066.CIR-17-0375. Epub 2017 Oct 16.
Immunotherapy is rapidly becoming a standard of care for many cancers. However, colorectal cancer had been generally resistant to immunotherapy, despite features in common with sensitive tumors. Observations of substantial clinical activity for checkpoint blockade in colorectal cancers with defective mismatch repair (microsatellite instability-high tumors) have reignited interest in the search for immunotherapies that could be extended to the larger microsatellite stable (MSS) population. The Cancer Research Institute and Fight Colorectal Cancer convened a group of scientists, clinicians, advocates, and industry experts in colorectal cancer and immunotherapy to compile ongoing research efforts, identify gaps in translational and clinical research, and provide a blueprint to advance immunotherapy. We identified lack of a T-cell inflamed phenotype (due to inadequate T-cell infiltration, inadequate T-cell activation, or T-cell suppression) as a broad potential explanation for failure of checkpoint blockade in MSS. The specific cellular and molecular underpinnings for these various mechanisms are unclear. Whether biomarkers with prognostic value, such as the immunoscores and IFN signatures, would also predict benefit for immunotherapies in MSS colon cancer is unknown, but if so, these and other biomarkers for measuring the potential for an immune response in patients with colorectal cancer will need to be incorporated into clinical guidelines. We have proposed a framework for research to identify immunologic factors that may be modulated to improve immunotherapy for colorectal cancer patients, with the goal that the biomarkers and treatment strategies identified will become part of the routine management of colorectal cancer. .
免疫疗法正在迅速成为许多癌症的标准治疗方法。然而,尽管结直肠癌与敏感肿瘤有共同特征,但它通常对免疫疗法具有抗性。在存在错配修复缺陷(微卫星不稳定高肿瘤)的结直肠癌中,检查点阻断具有显著临床活性的观察结果重新激发了人们对寻找免疫疗法的兴趣,这些免疫疗法可能扩展到更大的微卫星稳定(MSS)人群。癌症研究所和抗击结直肠癌协会召集了一组科学家、临床医生、倡导者和结直肠癌及免疫疗法领域的行业专家,以汇编正在进行的研究工作,确定转化和临床研究中的差距,并提供推进免疫疗法的蓝图。我们认为,缺乏 T 细胞炎症表型(由于 T 细胞浸润不足、T 细胞激活不足或 T 细胞抑制)是 MSS 中检查点阻断失败的广泛潜在解释。这些各种机制的具体细胞和分子基础尚不清楚。具有预后价值的生物标志物(如免疫评分和 IFN 特征)是否也可预测 MSS 结肠癌免疫治疗的益处尚不清楚,但是如果是这样,这些和其他用于衡量结直肠癌患者免疫反应潜力的生物标志物将需要纳入临床指南。我们已经提出了一个研究框架,以确定可能调节的免疫因素,以改善结直肠癌患者的免疫疗法,目标是确定的生物标志物和治疗策略将成为结直肠癌常规管理的一部分。