Targeted therapy for renal cell carcinoma: The next lap.

Q1 Environmental Science
Journal of Carcinogenesis Pub Date : 2014-02-20 eCollection Date: 2014-01-01 DOI:10.4103/1477-3163.127638
Ravindran Kanesvaran, Min-Han Tan
{"title":"Targeted therapy for renal cell carcinoma: The next lap.","authors":"Ravindran Kanesvaran,&nbsp;Min-Han Tan","doi":"10.4103/1477-3163.127638","DOIUrl":null,"url":null,"abstract":"<p><p>Advances in rationally targeted therapeutics over the last decade have transformed the clinical care of advanced kidney cancer. While oncologists consolidate the gains of the wave of new agents, comprising a panoply of anti-vascular endothelial growth factor multi-targeted tyrosine kinase inhibitors and inhibitors of the mammalian target of rapamycin (mTOR), there is an increasing sense that a plateau has been reached in the short term. It is sobering that all currently approved targeted therapies have not yielded durable remissions and remain palliative in intent. In the context of recent insights in kidney cancer biology, we review promising ongoing and future approaches for kidney cancer therapeutics aimed toward forging new paths in the systemic management of renal cell carcinoma. Broadly, candidate agents for such innovative strategies include immune check-point inhibitors, anti-cancer stem cell agents, next-generation anti-vascular endothelial growth factor receptor and anti-mTOR agents as well as more investigational agents in the preclinical and early clinical development settings. </p>","PeriodicalId":52464,"journal":{"name":"Journal of Carcinogenesis","volume":"13 ","pages":"3"},"PeriodicalIF":0.0000,"publicationDate":"2014-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4103/1477-3163.127638","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Carcinogenesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/1477-3163.127638","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Environmental Science","Score":null,"Total":0}
引用次数: 28

Abstract

Advances in rationally targeted therapeutics over the last decade have transformed the clinical care of advanced kidney cancer. While oncologists consolidate the gains of the wave of new agents, comprising a panoply of anti-vascular endothelial growth factor multi-targeted tyrosine kinase inhibitors and inhibitors of the mammalian target of rapamycin (mTOR), there is an increasing sense that a plateau has been reached in the short term. It is sobering that all currently approved targeted therapies have not yielded durable remissions and remain palliative in intent. In the context of recent insights in kidney cancer biology, we review promising ongoing and future approaches for kidney cancer therapeutics aimed toward forging new paths in the systemic management of renal cell carcinoma. Broadly, candidate agents for such innovative strategies include immune check-point inhibitors, anti-cancer stem cell agents, next-generation anti-vascular endothelial growth factor receptor and anti-mTOR agents as well as more investigational agents in the preclinical and early clinical development settings.

Abstract Image

肾细胞癌的靶向治疗:下一步。
在过去的十年中,合理靶向治疗的进步已经改变了晚期肾癌的临床治疗。虽然肿瘤学家巩固了新药物的成果,包括抗血管内皮生长因子多靶向酪氨酸激酶抑制剂和哺乳动物靶雷帕霉素(mTOR)抑制剂,但越来越多的人认为,短期内已经达到平台期。令人警醒的是,目前所有批准的靶向治疗都没有产生持久的缓解,并且仍然是姑息性的。在最近对肾癌生物学的见解的背景下,我们回顾了有希望的正在进行和未来的肾癌治疗方法,旨在为肾细胞癌的系统管理开辟新的途径。总的来说,这种创新策略的候选药物包括免疫检查点抑制剂、抗癌干细胞药物、下一代抗血管内皮生长因子受体和抗mtor药物,以及临床前和早期临床开发环境中的更多研究药物。
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 求助全文
来源期刊
Journal of Carcinogenesis
Journal of Carcinogenesis Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.50
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊介绍: Journal of Carcinogenesis considers manuscripts in many areas of carcinogenesis and Chemoprevention. Primary areas of interest to the journal include: physical and chemical carcinogenesis and mutagenesis; processes influencing or modulating carcinogenesis, such as DNA repair; genetics, nutrition, and metabolism of carcinogens; the mechanism of action of carcinogens and modulating agents; epidemiological studies; and, the formation, detection, identification, and quantification of environmental carcinogens. Manuscripts that contribute to the understanding of cancer prevention are especially encouraged for submission
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信