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结直肠癌的预后和预测分子生物标志物

Prognostic and predictive molecular biomarkers in colorectal cancer.

作者信息

Zhang Jianzhi, Zhu Hao, Liu Wentao, Miao Ji, Mao Yonghuan, Li Qiang

机构信息

Department of General Surgery, Affiliated Drum Tower Hospital, Nanjing University Medical School, Nanjing, China.

Department of General Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, China.

出版信息

Front Oncol. 2025 Apr 16;15:1532924. doi: 10.3389/fonc.2025.1532924. eCollection 2025.

DOI:10.3389/fonc.2025.1532924
PMID:40308511
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12040681/
Abstract

Precision medicine has brought revolutionary changes to the diagnosis and treatment of cancer patients, and is currently a hot and challenging research topic. Currently, the treatment regimens for most colorectal cancer (CRC) patients are mainly determined by several biomakers, including Microsatellite Instability (MSI), RAS, and BRAF. However, the roles of promising biomarkers such as HER-2, consensus molecular subtypes (CMS), and circulating tumor DNA (ctDNA) in CRC are not yet fully clear. Therefore, it is urgent to explore the potential of these emerging biomarkers in the diagnosis and treatment of CRC patients. In this paper, we discuss recent advances in CRC biomarkers, especially clinical data, and focus on the roles of biomarkers in prognosis, prediction, treatment strategies, and the intrinsic connections with clinical pathological features, hoping to promote better precision medicine for colorectal cancer.

摘要

精准医学给癌症患者的诊断和治疗带来了革命性变化,目前是一个热门且具有挑战性的研究课题。目前,大多数结直肠癌(CRC)患者的治疗方案主要由几种生物标志物决定,包括微卫星不稳定性(MSI)、RAS和BRAF。然而,有前景的生物标志物如HER-2、共识分子亚型(CMS)和循环肿瘤DNA(ctDNA)在CRC中的作用尚未完全明确。因此,迫切需要探索这些新兴生物标志物在CRC患者诊断和治疗中的潜力。在本文中,我们讨论了CRC生物标志物的最新进展,特别是临床数据,并重点关注生物标志物在预后、预测、治疗策略以及与临床病理特征的内在联系方面的作用,希望能促进更好的结直肠癌精准医学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e6d/12040681/f000a0034e27/fonc-15-1532924-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e6d/12040681/13fbf3cf7a99/fonc-15-1532924-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e6d/12040681/f000a0034e27/fonc-15-1532924-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e6d/12040681/13fbf3cf7a99/fonc-15-1532924-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e6d/12040681/f000a0034e27/fonc-15-1532924-g002.jpg

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Biomedicines. 2025 Aug 21;13(8):2038. doi: 10.3390/biomedicines13082038.

本文引用的文献

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Int J Clin Oncol. 2025 Apr;30(4):718-727. doi: 10.1007/s10147-024-02686-x. Epub 2025 Feb 27.
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Trastuzumab Plus Pertuzumab Versus Cetuximab Plus Irinotecan in Patients With Wild-Type, HER2-Positive, Metastatic Colorectal Cancer (S1613): A Randomized Phase II Trial.曲妥珠单抗联合帕妥珠单抗对比西妥昔单抗联合伊立替康治疗野生型、HER2阳性转移性结直肠癌患者(S1613):一项随机II期试验
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Clinical significance of combined tumour-infiltrating lymphocytes and microsatellite instability status in colorectal cancer: a systematic review and network meta-analysis.
结直肠癌中肿瘤浸润淋巴细胞与微卫星不稳定性状态的临床意义:系统评价和网络荟萃分析。
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Next-Generation Multitarget Stool DNA Test for Colorectal Cancer Screening.用于结直肠癌筛查的下一代多靶点粪便 DNA 检测。
N Engl J Med. 2024 Mar 14;390(11):984-993. doi: 10.1056/NEJMoa2310336.
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A Cell-free DNA Blood-Based Test for Colorectal Cancer Screening.基于无细胞游离 DNA 的血液检测用于结直肠癌筛查。
N Engl J Med. 2024 Mar 14;390(11):973-983. doi: 10.1056/NEJMoa2304714.
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Nat Med. 2024 Mar;30(3):730-739. doi: 10.1038/s41591-023-02791-w. Epub 2024 Feb 12.
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