• 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

结直肠癌:新兴分子认识如何影响治疗决策。

Colorectal cancer: how emerging molecular understanding affects treatment decisions.

出版信息

Oncology (Williston Park). 2014 Feb;28(2):110-8.

PMID:24701697
Abstract

The medical treatment of metastatic colorectal cancer (mCRC) has advanced significantly over the last 10 years as the result of the introduction of several active cytotoxic and biologic agents into standard clinical practice. Several recent phase III trials reported median overall survival data exceeding 30 months, an achievement inconceivable only 5 years ago.The first major step forward in the medical management of mCRC was provided by the addition of irinotecan and oxaliplatin to fluorouracil-based therapy; this increased survival from about 12 months to about 20 months.The introduction of biologic agents such as vascular endothelial growth factor inhibitors and epidermal growth factor inhibitors further increased survival--to more than 2 years in prospective trials. Recently, an expanding array of molecular prognostic and predictive biomarkers have been developed that are being integrated into clinical practice. In this review we discuss the current treatment options in metastatic colon cancer, with a special focus on biologic agents and how molecular understanding guides treatment decisions.

摘要

过去 10 年来,转移性结直肠癌(mCRC)的治疗取得了显著进展,这得益于几种有效的细胞毒性药物和生物制剂被引入标准临床实践。最近的几项 III 期临床试验报告了中位总生存期数据超过 30 个月,这在 5 年前是难以想象的。mCRC 医学管理的第一个重大进展是在氟尿嘧啶为基础的治疗中加入伊立替康和奥沙利铂;这将生存时间从大约 12 个月延长到了大约 20 个月。生物制剂如血管内皮生长因子抑制剂和表皮生长因子抑制剂的引入进一步提高了生存率——在前瞻性试验中超过 2 年。最近,大量新的分子预后和预测生物标志物已经被开发出来,并被整合到临床实践中。在这篇综述中,我们讨论了转移性结肠癌的当前治疗选择,特别关注生物制剂以及分子认识如何指导治疗决策。

相似文献

1
Colorectal cancer: how emerging molecular understanding affects treatment decisions.结直肠癌:新兴分子认识如何影响治疗决策。
Oncology (Williston Park). 2014 Feb;28(2):110-8.
2
Targeted therapy in metastatic colorectal cancer -- an example of personalised medicine in action.转移性结直肠癌的靶向治疗——个体化医学的实践范例。
Cancer Treat Rev. 2013 Oct;39(6):592-601. doi: 10.1016/j.ctrv.2012.12.011. Epub 2013 Jan 31.
3
An update on treatment advances for the first-line therapy of metastatic colorectal cancer.转移性结直肠癌一线治疗的治疗进展更新
Cancer J. 2007 Sep-Oct;13(5):276-81. doi: 10.1097/PPO.0b013e3181570062.
4
Targeted therapy for metastatic colorectal cancer: role of aflibercept.转移性结直肠癌的靶向治疗:阿柏西普的作用。
Clin Colorectal Cancer. 2013 Jun;12(2):73-85. doi: 10.1016/j.clcc.2012.08.001. Epub 2012 Oct 24.
5
[Chemotherapy for metastatic colorectal cancer].[转移性结直肠癌的化疗]
Gan To Kagaku Ryoho. 2008 Sep;35(9):1467-74.
6
Personalizing therapy for colorectal cancer.对结直肠癌进行个体化治疗。
Clin Gastroenterol Hepatol. 2014 Jan;12(1):139-44. doi: 10.1016/j.cgh.2013.08.040. Epub 2013 Sep 8.
7
Targeting metastatic colorectal cancer in 2008: a long way from 5-FU.2008年针对转移性结直肠癌的治疗:与5-氟尿嘧啶相比仍有很大差距。
Oncology (Williston Park). 2008 Apr 15;22(4):456-62; discussion 462-3, 467-8, 474 passim.
8
Emerging VEGF-receptor inhibitors for colorectal cancer.新型血管内皮生长因子受体抑制剂在结直肠癌中的应用。
Expert Opin Emerg Drugs. 2013 Mar;18(1):25-37. doi: 10.1517/14728214.2013.749856. Epub 2012 Dec 6.
9
Treatment of metastatic colorectal cancer: from cytotoxic agents to molecular agents and multitargeted strategies.转移性结直肠癌的治疗:从细胞毒性药物到分子药物及多靶点策略
Oncology (Williston Park). 2006 Dec;20(14 Suppl 10):11-9.
10
Molecular markers in the treatment of metastatic colorectal cancer.分子标志物在转移性结直肠癌治疗中的应用。
Cancer J. 2010 May-Jun;16(3):262-72. doi: 10.1097/PPO.0b013e3181e07738.

引用本文的文献

1
KCTD15 acts as an anti-tumor factor in colorectal cancer cells downstream of the demethylase FTO and the m6A reader YTHDF2.KCTD15 在去甲基化酶 FTO 和 m6A 阅读器 YTHDF2 的下游作为结直肠癌细胞中的抗肿瘤因子发挥作用。
Commun Biol. 2024 Mar 4;7(1):262. doi: 10.1038/s42003-024-05880-9.
2
Curcumin targets miR-134-5p to suppress the progression of colorectal cancer through regulating the CDCA3/CDK1 pathway.姜黄素靶向miR-134-5p,通过调节CDCA3/CDK1通路抑制结直肠癌进展。
Naunyn Schmiedebergs Arch Pharmacol. 2024 Jan;397(1):109-122. doi: 10.1007/s00210-023-02584-5. Epub 2023 Jun 27.
3
Platelet-derived growth factor (PDGF) cross-signaling via non-corresponding receptors indicates bypassed signaling in colorectal cancer.
血小板衍生生长因子 (PDGF) 通过非对应受体的交叉信号转导表明结直肠癌中的信号转导旁路。
Oncotarget. 2022 Oct 19;13:1140-1152. doi: 10.18632/oncotarget.28281.
4
Long non‑coding RNA SNHG20 promotes colorectal cancer cell proliferation, migration and invasion via miR‑495/STAT3 axis.长链非编码 RNA SNHG20 通过 miR-495/STAT3 轴促进结直肠癌细胞的增殖、迁移和侵袭。
Mol Med Rep. 2021 Jan;23(1). doi: 10.3892/mmr.2020.11669. Epub 2020 Nov 12.
5
variants C3435T and T129C are not associated with colorectal cancer risk.C3435T和T129C变体与结直肠癌风险无关。
Afr Health Sci. 2019 Sep;19(3):2476-2483. doi: 10.4314/ahs.v19i3.23.
6
Calcium-Activated Chloride Channel A4 (CLCA4) Plays Inhibitory Roles in Invasion and Migration Through Suppressing Epithelial-Mesenchymal Transition via PI3K/AKT Signaling in Colorectal Cancer.钙激活氯离子通道 A4(CLCA4)通过抑制 PI3K/AKT 信号通路抑制结直肠癌细胞上皮间质转化从而发挥抑制侵袭和迁移的作用。
Med Sci Monit. 2019 Jun 5;25:4176-4185. doi: 10.12659/MSM.914195.
7
MiR-208a-3p functions as an oncogene in colorectal cancer by targeting PDCD4.miR-208a-3p 通过靶向 PDCD4 在结直肠癌中发挥癌基因作用。
Biosci Rep. 2019 Apr 16;39(4). doi: 10.1042/BSR20181598. Print 2019 Apr 30.
8
Molecular characterization and biomarker identification in colorectal cancer: Toward realization of the precision medicine dream.结直肠癌的分子特征与生物标志物鉴定:迈向精准医学梦想的实现
Cancer Manag Res. 2018 Nov 19;10:5895-5908. doi: 10.2147/CMAR.S162967. eCollection 2018.
9
Upregulation of AKIP1 contributes to metastasis and progression and predicts poor prognosis of patients with colorectal cancer.AKIP1的上调促进了结直肠癌的转移和进展,并预示着患者的预后不良。
Onco Targets Ther. 2018 Oct 11;11:6795-6801. doi: 10.2147/OTT.S151952. eCollection 2018.
10
PUMA mediates the anti-cancer effect of osimertinib in colon cancer cells.PUMA介导奥希替尼在结肠癌细胞中的抗癌作用。
Onco Targets Ther. 2017 Nov 3;10:5281-5288. doi: 10.2147/OTT.S139382. eCollection 2017.