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Phase I Dose-Escalation and -Expansion Study of Telisotuzumab (ABT-700), an Anti-c-Met Antibody, in Patients with Advanced Solid Tumors.Telisotuzumab(ABT-700),一种抗 c-Met 抗体,在晚期实体瘤患者中的 I 期剂量递增和扩展研究。
Mol Cancer Ther. 2020 May;19(5):1210-1217. doi: 10.1158/1535-7163.MCT-19-0529. Epub 2020 Mar 3.
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FOLFOX alone or combined with rilotumumab or panitumumab as first-line treatment for patients with advanced gastroesophageal adenocarcinoma (PRODIGE 17-ACCORD 20-MEGA): a randomised, open-label, three-arm phase II trial.FOLFOX 单药或联合 ri lotumumab 或 panitumumab 一线治疗晚期胃食管腺癌患者(PRODIGE 17-ACCORD 20-MEGA):一项随机、开放标签、三臂 II 期试验。
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Rilotumumab plus epirubicin, cisplatin, and capecitabine as first-line therapy in advanced MET-positive gastric or gastro-oesophageal junction cancer (RILOMET-1): a randomised, double-blind, placebo-controlled, phase 3 trial.瑞罗西单抗联合表柔比星、顺铂和卡培他滨作为晚期MET阳性胃癌或胃食管交界癌的一线治疗(RILOMET-1):一项随机、双盲、安慰剂对照的3期试验。
Lancet Oncol. 2017 Nov;18(11):1467-1482. doi: 10.1016/S1470-2045(17)30566-1. Epub 2017 Sep 25.
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Targeting c-MET in gastrointestinal tumours: rationale, opportunities and challenges.针对胃肠道肿瘤的 c-MET:原理、机会和挑战。
Nat Rev Clin Oncol. 2017 Sep;14(9):562-576. doi: 10.1038/nrclinonc.2017.40. Epub 2017 Apr 4.
5
A Phase II Randomized Trial (GO27827) of First-Line FOLFOX Plus Bevacizumab with or Without the MET Inhibitor Onartuzumab in Patients with Metastatic Colorectal Cancer.一项针对转移性结直肠癌患者的二线随机试验(GO27827):一线FOLFOX联合贝伐单抗,联合或不联合MET抑制剂奥那珠单抗。
Oncologist. 2017 Mar;22(3):264-271. doi: 10.1634/theoncologist.2016-0223. Epub 2017 Feb 16.
6
A Randomized Phase II Study of FOLFOX With or Without the MET Inhibitor Onartuzumab in Advanced Adenocarcinoma of the Stomach and Gastroesophageal Junction.一项关于FOLFOX联合或不联合MET抑制剂奥那珠单抗治疗晚期胃及胃食管交界腺癌的随机II期研究。
Oncologist. 2016 Sep;21(9):1085-90. doi: 10.1634/theoncologist.2016-0038. Epub 2016 Jul 8.
7
MET-Driven Resistance to Dual EGFR and BRAF Blockade May Be Overcome by Switching from EGFR to MET Inhibition in BRAF-Mutated Colorectal Cancer.MET 驱动的对双重 EGFR 和 BRAF 阻断的耐药性可通过在 BRAF 突变结直肠癌中从 EGFR 抑制转换为 MET 抑制来克服。
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8
Resistance to the c-Met inhibitor KRC-108 induces the epithelial transition of gastric cancer cells.对c-Met抑制剂KRC-108的耐药性诱导胃癌细胞发生上皮转化。
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9
Anti-c-Met monoclonal antibody ABT-700 breaks oncogene addiction in tumors with MET amplification.抗c-Met单克隆抗体ABT-700可打破MET扩增肿瘤中的癌基因成瘾性。
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Gastric Cancer: New Drugs - New Strategies.胃癌:新药 - 新策略
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胃癌中靶向HGF/c-Met通路的研究进展

Current advances of targeting HGF/c-Met pathway in gastric cancer.

作者信息

Anestis Aristomenis, Zoi Ilianna, Karamouzis Michalis V

机构信息

Molecular Oncology Unit, Department of Biological Chemistry, 'Laiko' General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

First Department of Internal Medicine, 'Laiko' General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Ann Transl Med. 2018 Jun;6(12):247. doi: 10.21037/atm.2018.04.42.

DOI:10.21037/atm.2018.04.42
PMID:30069449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6046293/
Abstract

Despite the advances in systemic chemotherapy, gastric adenocarcinoma (GC) remains the third most common cause of cancer-related deaths with poor prognosis. The heterogeneity of GC indicates that novel biomarkers should be established in order to further classify tumors and develop individual targeted therapies. High-quality preclinical and clinical research has demonstrated that growth factor (HGF)-hepatocyte growth factor receptor (c-Met) pathway plays a pivotal role on the growth, survival and invasiveness of GC. In particular, aberrant activation of HGF/c-Met signaling pathway has been associated with poor clinical outcomes, suggesting the therapeutic potential of c-Met. This has stimulated the development and evaluation of a number of c-Met targeted agents in an advance disease setting. In this review, we summarize the current state of the art in the advances on the inhibition of c-Met pathway, with particular emphasis on the clinical testing of c-Met targeted therapeutic agents. Furthermore, we discuss the challenges facing the incorporation of c-Met targeted agents in randomized trials, with the idea that the definition of the appropriate genetic and molecular context for the use of these agents remains the priority.

摘要

尽管全身化疗取得了进展,但胃腺癌(GC)仍是癌症相关死亡的第三大常见原因,预后较差。GC的异质性表明,应建立新的生物标志物,以便进一步对肿瘤进行分类并开发个体化的靶向治疗。高质量的临床前和临床研究表明,生长因子(HGF)-肝细胞生长因子受体(c-Met)通路在GC的生长、存活和侵袭中起关键作用。特别是,HGF/c-Met信号通路的异常激活与不良临床结果相关,提示了c-Met的治疗潜力。这刺激了多种c-Met靶向药物在晚期疾病环境中的开发和评估。在本综述中,我们总结了c-Met通路抑制方面的最新进展,特别强调了c-Met靶向治疗药物的临床试验。此外,我们讨论了将c-Met靶向药物纳入随机试验所面临的挑战,认为确定使用这些药物的合适基因和分子背景仍然是首要任务。