Trastuzumab emtansine is the standard second-line treatment following horizontal blockade in first line of advanced HER-2 positive breast cancer: A plant that has still to grow

L. Montella, S. Prete, P. Bove
{"title":"Trastuzumab emtansine is the standard second-line treatment following horizontal blockade in first line of advanced HER-2 positive breast cancer: A plant that has still to grow","authors":"L. Montella, S. Prete, P. Bove","doi":"10.15761/icst.1000302","DOIUrl":null,"url":null,"abstract":"From 2001 until now, treatment of HER-2 expressing breast cancer is radically changed. The cardinal role of HER-2 antigen [1] and the power of blocking HER-2 signalling by trastuzumab [2] have been increasingly recognized as the bricks on which a robust therapeutic strategy could be built. In fact, Cleopatra study in first-line [3], Emilia in second line [4] and Th3resa [5] in third line are only confirmative of this statement. The novel antibody pertuzumab, added to the trastuzumab in the triplet of Cleopatra study, significantly increases overall survival and progression-free survival as never before [3]. Trastuzumabado-emtansine (TDM-1) is an anti-HER2 antibody-drug conjugate (ADC). TDM-1 was pharmacologically developed on the solid axis of trastuzumab because the chemotherapeutic emtansine is too toxic to be used alone. This means that HER-2 pathway remains the way to arrive to tumor but the machine was empowered by a chemotherapeutic able to enhance the killing cell rate.","PeriodicalId":90850,"journal":{"name":"Integrative cancer science and therapeutics","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative cancer science and therapeutics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/icst.1000302","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

From 2001 until now, treatment of HER-2 expressing breast cancer is radically changed. The cardinal role of HER-2 antigen [1] and the power of blocking HER-2 signalling by trastuzumab [2] have been increasingly recognized as the bricks on which a robust therapeutic strategy could be built. In fact, Cleopatra study in first-line [3], Emilia in second line [4] and Th3resa [5] in third line are only confirmative of this statement. The novel antibody pertuzumab, added to the trastuzumab in the triplet of Cleopatra study, significantly increases overall survival and progression-free survival as never before [3]. Trastuzumabado-emtansine (TDM-1) is an anti-HER2 antibody-drug conjugate (ADC). TDM-1 was pharmacologically developed on the solid axis of trastuzumab because the chemotherapeutic emtansine is too toxic to be used alone. This means that HER-2 pathway remains the way to arrive to tumor but the machine was empowered by a chemotherapeutic able to enhance the killing cell rate.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
曲妥珠单抗emtansine是晚期HER-2阳性乳腺癌一线水平阻断后的标准二线治疗:一种仍在生长的植物
从2001年至今,表达HER-2的乳腺癌的治疗方法发生了根本性的变化。HER-2抗原[1]的主要作用和曲妥珠单抗[2]阻断HER-2信号传导的能力越来越被认为是建立强大治疗策略的基础。事实上,第一行[3]中的克利奥帕特拉研究,第二行[4]中的艾米莉亚研究和第三行Th3resa[5]研究都只是证实了这一说法。在克利奥帕特拉三联体研究中,新型抗体帕妥珠单抗加入曲妥珠单抗,显著提高了总生存期和无进展生存期,这在2010年之前是前所未有的。曲妥珠单抗-emtansine (TDM-1)是一种抗her2抗体-药物偶联物(ADC)。TDM-1是在曲妥珠单抗的实体轴上进行药理学开发的,因为化疗药物艾姆坦辛毒性太大,不能单独使用。这意味着HER-2途径仍然是到达肿瘤的途径,但这台机器被一种能够提高杀伤细胞率的化疗赋予了力量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
APE1/Ref-1 with reducing activity induces mesenchymal-to-epithelial transition in TNF-α-stimulated breast cancer cells Exploiting mechanism-informed phenotypic screening for development of next-generation antimitotic phytochemicals Prospects for colorectal cancer prevention targeting intestinal microbiome Sclerosing Pneumocytoma: A Carcinoma Mimicker Phytotherapy and oncology. A short review
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1