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本文引用的文献

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Molecular markers identify subtypes of stage III colon cancer associated with patient outcomes.分子标志物可识别与患者预后相关的III期结肠癌亚型。
Gastroenterology. 2015 Jan;148(1):88-99. doi: 10.1053/j.gastro.2014.09.041. Epub 2014 Oct 8.
2
Progression-free survival remains poor over sequential lines of systemic therapy in patients with BRAF-mutated colorectal cancer.在BRAF突变型结直肠癌患者中,经多线序贯全身治疗后的无进展生存期仍然较差。
Clin Colorectal Cancer. 2014 Sep;13(3):164-71. doi: 10.1016/j.clcc.2014.06.001. Epub 2014 Jun 23.
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Patient and tumor characteristics and BRAF and KRAS mutations in colon cancer, NCCTG/Alliance N0147.结肠癌患者和肿瘤特征以及 BRAF 和 KRAS 突变,NCCTG/Alliance N0147。
J Natl Cancer Inst. 2014 Jun 12;106(7). doi: 10.1093/jnci/dju106. Print 2014 Jul.
4
BRAF mutation predicts for poor outcomes after metastasectomy in patients with metastatic colorectal cancer.BRAF突变预示着转移性结直肠癌患者行转移灶切除术后预后不良。
Cancer. 2014 Aug 1;120(15):2316-24. doi: 10.1002/cncr.28729. Epub 2014 Apr 15.
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Microsatellite instability and BRAF mutation testing in colorectal cancer prognostication.结直肠癌预后评估中的微卫星不稳定性和 BRAF 基因突变检测。
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Resistance to BRAF inhibition in BRAF-mutant colon cancer can be overcome with PI3K inhibition or demethylating agents.BRAF 突变型结肠癌对 BRAF 抑制的耐药性可以通过抑制 PI3K 或去甲基化剂来克服。
Clin Cancer Res. 2013 Feb 1;19(3):657-67. doi: 10.1158/1078-0432.CCR-11-1446. Epub 2012 Dec 18.
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EGFR-mediated re-activation of MAPK signaling contributes to insensitivity of BRAF mutant colorectal cancers to RAF inhibition with vemurafenib.表皮生长因子受体(EGFR)介导的丝裂原活化蛋白激酶(MAPK)信号的重新激活有助于解释 BRAF 突变的结直肠癌对威罗菲尼(vemurafenib)抑制 RAF 激酶的不敏感性。
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Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: pooled analysis of the CRYSTAL and OPUS randomised clinical trials.西妥昔单抗联合化疗作为 KRAS 野生型转移性结直肠癌的一线治疗:CRYSTAL 和 OPUS 随机临床试验的汇总分析。
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Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR.结直肠癌对 BRAF(V600E)抑制的无应答性通过 EGFR 的反馈激活。
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BRAF mutations in colorectal cancer are associated with distinct clinical characteristics and worse prognosis.结直肠癌中的 BRAF 突变与独特的临床特征和较差的预后相关。
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BRAF 突变型结直肠癌作为结直肠癌的一个独特亚组:临床特征、临床行为及对靶向治疗的反应

BRAF mutant colorectal cancer as a distinct subset of colorectal cancer: clinical characteristics, clinical behavior, and response to targeted therapies.

作者信息

Clarke Callisia N, Kopetz E Scott

机构信息

1 Department of Surgical Oncology, 2 Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Gastrointest Oncol. 2015 Dec;6(6):660-7. doi: 10.3978/j.issn.2078-6891.2015.077.

DOI:10.3978/j.issn.2078-6891.2015.077
PMID:26697199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4671844/
Abstract

Despite new and more effective cytotoxic chemotherapy, limitations to conventional agents have been reached in a subset of patients with advanced colorectal cancer (CRC). The identification of novel prognostic and predictive biomarkers to guide individualized treatment plans is critical to overcoming therapeutic resistance. Mutation of the BRAF proto-oncogene is linked to a variety of cancers and is increasingly being used as a prognostic tool and therapeutic target. This paper is a comprehensive review of the literature that summarizes the clinical, pathologic, and molecular features of BRAF mutated CRC that support the hypothesis that BRAF mutant cancers represent a distinct subset of CRC with its own clinical implications with regard to prognosis, treatments and emerging therapeutic strategies.

摘要

尽管有了新型且更有效的细胞毒性化疗药物,但在一部分晚期结直肠癌(CRC)患者中,传统药物已达到其局限性。识别新的预后和预测生物标志物以指导个体化治疗方案对于克服治疗耐药性至关重要。BRAF原癌基因的突变与多种癌症相关,并且越来越多地被用作预后工具和治疗靶点。本文是一篇文献综述,总结了BRAF突变型CRC的临床、病理和分子特征,支持以下假设:BRAF突变型癌症代表CRC的一个独特亚组,在预后、治疗和新兴治疗策略方面有其自身的临床意义。