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本文引用的文献

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Effect of Modified Vaccinia Ankara-5T4 and Low-Dose Cyclophosphamide on Antitumor Immunity in Metastatic Colorectal Cancer: A Randomized Clinical Trial.改良安卡拉痘苗病毒-5T4 联合低剂量环磷酰胺对转移性结直肠癌患者抗肿瘤免疫的影响:一项随机临床试验。
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Prime-Boost Immunization Eliminates Metastatic Colorectal Cancer by Producing High-Avidity Effector CD8 T Cells.初免-加强免疫通过产生高亲和力效应性CD8 T细胞消除转移性结直肠癌。
J Immunol. 2017 May 1;198(9):3507-3514. doi: 10.4049/jimmunol.1502672. Epub 2017 Mar 24.
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Phase 1 study of OCV-C02, a peptide vaccine consisting of two peptide epitopes for refractory metastatic colorectal cancer.OCV-C02的1期研究,OCV-C02是一种由两种肽表位组成的肽疫苗,用于难治性转移性结直肠癌。
Cancer Sci. 2017 May;108(5):1013-1021. doi: 10.1111/cas.13227. Epub 2017 May 11.
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Elements of cancer immunity and the cancer-immune set point.癌症免疫的要素和癌症免疫基准。
Nature. 2017 Jan 18;541(7637):321-330. doi: 10.1038/nature21349.
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Cancer Statistics, 2017.《2017 年癌症统计》
CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
8
Targeting Carcinoembryonic Antigen with DNA Vaccination: On-Target Adverse Events Link with Immunologic and Clinical Outcomes.通过DNA疫苗靶向癌胚抗原:靶向性不良事件与免疫和临床结果的关联
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Safety, efficacy, and immunogenicity of VGX-3100, a therapeutic synthetic DNA vaccine targeting human papillomavirus 16 and 18 E6 and E7 proteins for cervical intraepithelial neoplasia 2/3: a randomised, double-blind, placebo-controlled phase 2b trial.VGX-3100用于治疗宫颈上皮内瘤变2/3的安全性、有效性及免疫原性:一项针对人乳头瘤病毒16和18 E6及E7蛋白的治疗性合成DNA疫苗的随机、双盲、安慰剂对照2b期试验
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Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy.微卫星不稳定结直肠癌中 CD8+T 细胞浸润密度与框移突变的相关性:个体化免疫治疗的理由。
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转移性结直肠癌的免疫治疗方案。

Immunotherapy regimens for metastatic colorectal carcinomas.

机构信息

a Departments of Pharmacology and Experimental Therapeutics , Thomas Jefferson University , Philadelphia , PA , USA.

b Department of Medical Oncology , Thomas Jefferson University , Philadelphia , PA , USA.

出版信息

Hum Vaccin Immunother. 2018 Feb 1;14(2):250-254. doi: 10.1080/21645515.2017.1397244. Epub 2017 Dec 6.

DOI:10.1080/21645515.2017.1397244
PMID:29083978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5806658/
Abstract

Metastatic colorectal cancer (mCRC) is a leading cause of cancer-related mortality with a 5-year overall survival rate of 13%. Despite recent advances in cancer immunotherapy, only the minority of CRC patients (<15%) with microsatellite instability can potentially benefit from immune checkpoint inhibitors, the only immunotherapy currently approved for mCRC. In that context, there is an unmet need to improve survival in mCRC. Our ever-increasing understanding of the immune system and its interactions with cancer has allowed development of multiple strategies to potentially improve outcomes in the majority of mCRC patients. Various approaches to manipulate patient immunity to recognize and kill colorectal cancer cells are being explored simultaneously, with combination therapies likely being the most effective. Ideally, therapies would target tumor-restricted antigens selectively found in tumors, but shielded from immune attack in normal tissues, to mount an effective cytotoxic T-cell response, while also overcoming cellular and molecular inhibitory pathways, self-tolerance, and T-cell exhaustion. Here, we provide a brief overview of the most promising immunotherapy candidates in mCRC and their strategies to produce a lasting immune response and clinical benefit in patients with mCRC.

摘要

转移性结直肠癌 (mCRC) 是导致癌症相关死亡的主要原因,其 5 年总生存率为 13%。尽管癌症免疫疗法最近取得了进展,但只有少数微卫星不稳定的 CRC 患者 (<15%) 可能受益于免疫检查点抑制剂,这是目前唯一批准用于 mCRC 的免疫疗法。在这种情况下,提高 mCRC 的生存率是当务之急。我们对免疫系统及其与癌症相互作用的理解不断加深,为提高大多数 mCRC 患者的治疗效果提供了多种策略。目前正在同时探索多种操纵患者免疫以识别和杀死结直肠癌细胞的方法,联合治疗可能是最有效的。理想情况下,治疗方法应针对肿瘤中特有的肿瘤限制性抗原,同时保护正常组织免受免疫攻击,以引发有效的细胞毒性 T 细胞反应,同时克服细胞和分子抑制途径、自身耐受和 T 细胞衰竭。在这里,我们简要概述了 mCRC 中最有前途的免疫治疗候选药物及其策略,以在 mCRC 患者中产生持久的免疫反应和临床获益。