• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

推进结直肠癌免疫治疗的蓝图。

A Blueprint to Advance Colorectal Cancer Immunotherapies.

机构信息

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland.

Cancer Research Institute, New York, New York.

出版信息

Cancer Immunol Res. 2017 Nov;5(11):942-949. doi: 10.1158/2326-6066.CIR-17-0375. Epub 2017 Oct 16.

DOI:10.1158/2326-6066.CIR-17-0375
PMID:29038296
Abstract

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. .

摘要

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。

相似文献

1
A Blueprint to Advance Colorectal Cancer Immunotherapies.推进结直肠癌免疫治疗的蓝图。
Cancer Immunol Res. 2017 Nov;5(11):942-949. doi: 10.1158/2326-6066.CIR-17-0375. Epub 2017 Oct 16.
2
Immunotherapy for the treatment of colorectal cancer.免疫疗法治疗结直肠癌。
J Surg Oncol. 2021 Mar;123(3):760-774. doi: 10.1002/jso.26357.
3
Clinical Application of Adaptive Immune Therapy in MSS Colorectal Cancer Patients.适应性免疫治疗在 MSS 结直肠癌患者中的临床应用。
Front Immunol. 2021 Oct 13;12:762341. doi: 10.3389/fimmu.2021.762341. eCollection 2021.
4
[Going beyond microsatellite instability for immunotherapy in metastatic colorectal cancer: Consensus molecular subtypes and tumor mutational burden].[转移性结直肠癌免疫治疗超越微卫星不稳定性:共识分子亚型与肿瘤突变负荷]
Bull Cancer. 2019 Feb;106(2):151-161. doi: 10.1016/j.bulcan.2018.09.008. Epub 2019 Jan 11.
5
Is There a Role for Programmed Death Ligand-1 Testing and Immunotherapy in Colorectal Cancer With Microsatellite Instability? Part II-The Challenge of Programmed Death Ligand-1 Testing and Its Role in Microsatellite Instability-High Colorectal Cancer.程序性死亡配体-1检测及免疫疗法在微卫星不稳定型结直肠癌中是否有作用?第二部分——程序性死亡配体-1检测的挑战及其在微卫星高度不稳定型结直肠癌中的作用
Arch Pathol Lab Med. 2018 Jan;142(1):26-34. doi: 10.5858/arpa.2017-0041-RA. Epub 2017 Nov 9.
6
Genomics and emerging biomarkers for immunotherapy of colorectal cancer.结直肠癌免疫治疗的基因组学和新兴生物标志物。
Semin Cancer Biol. 2018 Oct;52(Pt 2):189-197. doi: 10.1016/j.semcancer.2018.02.010. Epub 2018 Mar 1.
7
Molecular and Radiological Features of Microsatellite Stable Colorectal Cancer Cases With Dramatic Responses to Immunotherapy.分子和放射学特征与结直肠癌免疫治疗反应显著相关的微卫星稳定型病例
Anticancer Res. 2021 Jun;41(6):2985-2992. doi: 10.21873/anticanres.15080.
8
Immune Microenvironment in Microsatellite-Instable Endometrial Cancers: Hereditary or Sporadic Origin Matters.微卫星不稳定型子宫内膜癌的免疫微环境:遗传或散发性起源很重要。
Clin Cancer Res. 2017 Aug 1;23(15):4473-4481. doi: 10.1158/1078-0432.CCR-16-2655. Epub 2017 Mar 6.
9
The colorectal cancer immune microenvironment and approach to immunotherapies.结直肠癌免疫微环境与免疫治疗方法
Future Oncol. 2017 Aug;13(18):1633-1647. doi: 10.2217/fon-2017-0145. Epub 2017 Aug 22.
10
Where We Stand With Immunotherapy in Colorectal Cancer: Deficient Mismatch Repair, Proficient Mismatch Repair, and Toxicity Management.我们在结直肠癌免疫治疗中的立场:错配修复缺陷、错配修复 proficient 及毒性管理
Am Soc Clin Oncol Educ Book. 2018 May 23;38:239-247. doi: 10.1200/EDBK_200821.

引用本文的文献

1
Understanding the cellular and molecular heterogeneity in colorectal cancer through the use of single-cell RNA sequencing.通过单细胞RNA测序了解结直肠癌中的细胞和分子异质性。
Transl Oncol. 2025 May;55:102374. doi: 10.1016/j.tranon.2025.102374. Epub 2025 Mar 30.
2
The immunopeptidome of colon cancer cells treated with topoisomerase inhibiting drug reveals differential as well as common endogenous protein sampling and display of MHC I-associated peptides.用拓扑异构酶抑制药物处理的结肠癌细胞的免疫肽组揭示了不同以及常见的内源性蛋白质取样和MHC I相关肽的展示。
Mol Cell Oncol. 2025 Mar 3;12(1):2471640. doi: 10.1080/23723556.2025.2471640. eCollection 2025.
3
Mendelian randomization study identifying immune cell phenotypes associated with breast cancer risk.
孟德尔随机化研究确定与乳腺癌风险相关的免疫细胞表型。
Discov Oncol. 2025 Feb 19;16(1):205. doi: 10.1007/s12672-025-01963-z.
4
Mismatch repair-proficient tumor footprints in the sands of immune desert: mechanistic constraints and precision platforms.错配修复 proficient 肿瘤足迹在免疫荒漠的沙中:机械约束和精确平台。
Front Immunol. 2024 Jul 19;15:1414376. doi: 10.3389/fimmu.2024.1414376. eCollection 2024.
5
Myeloid‑derived suppressor cells: Key immunosuppressive regulators and therapeutic targets in colorectal cancer (Review).髓源性抑制细胞:结直肠癌中关键的免疫抑制调节因子和治疗靶点(综述)。
Int J Oncol. 2024 Sep;65(3). doi: 10.3892/ijo.2024.5673. Epub 2024 Jul 26.
6
Extracellular matrix stiffness and tumor-associated macrophage polarization: new fields affecting immune exclusion.细胞外基质硬度与肿瘤相关巨噬细胞极化:影响免疫排斥的新领域。
Cancer Immunol Immunother. 2024 May 2;73(6):115. doi: 10.1007/s00262-024-03675-9.
7
It's high-time to re-evaluate the value of induced-chemotherapy for reinforcing immunotherapy in colorectal cancer.现在是重新评估诱导化疗在结直肠癌中增强免疫治疗价值的时候了。
Front Immunol. 2023 Oct 18;14:1241208. doi: 10.3389/fimmu.2023.1241208. eCollection 2023.
8
Interference with pathways activated by topoisomerase inhibition alters the surface expression of PD-L1 and MHC I in colon cancer cells.对拓扑异构酶抑制所激活通路的干扰会改变结肠癌细胞中PD-L1和MHC I的表面表达。
Oncol Lett. 2022 Dec 9;25(1):41. doi: 10.3892/ol.2022.13628. eCollection 2023 Jan.
9
A comprehensive review on RNA interference-mediated targeting of interleukins and its potential therapeutic implications in colon cancer.RNA干扰介导的白细胞介素靶向作用及其在结肠癌中的潜在治疗意义的综合综述。
3 Biotech. 2023 Jan;13(1):18. doi: 10.1007/s13205-022-03421-x. Epub 2022 Dec 20.
10
CD8+ T cell-associated genes MS4A1 and TNFRSF17 are prognostic markers and inhibit the progression of colon cancer.CD8 + T细胞相关基因MS4A1和TNFRSF17是预后标志物,并抑制结肠癌的进展。
Front Oncol. 2022 Sep 20;12:941208. doi: 10.3389/fonc.2022.941208. eCollection 2022.