Emerging Antibody-Drug Conjugate Therapies and Targets for Metastatic Renal Cell Carcinoma

IF 1.1 Q4 ONCOLOGY
Kidney Cancer Pub Date : 2023-12-29 DOI:10.3233/kca-230012
Harrison C. Gottlich, Reza Nabavizadeh, Mihai Dumbrava, Rodrigo Rodrigues Pessoa, Ahmed M. Mahmoud, Ishita Garg, Jacob J. Orme, B. A. Costello, John Cheville, Fabrice Lucien
{"title":"Emerging Antibody-Drug Conjugate Therapies and Targets for Metastatic Renal Cell Carcinoma","authors":"Harrison C. Gottlich, Reza Nabavizadeh, Mihai Dumbrava, Rodrigo Rodrigues Pessoa, Ahmed M. Mahmoud, Ishita Garg, Jacob J. Orme, B. A. Costello, John Cheville, Fabrice Lucien","doi":"10.3233/kca-230012","DOIUrl":null,"url":null,"abstract":"Background: Approximately 30% of renal cell carcinoma (RCC) cases present with de novo metastatic disease, while 20% to 30% of those with localized disease will develop metastases following surgical resection. Various drug classes have been investigated to treat RCC, including cytokine-based therapies, small molecule Vascular Endothelial Growth Factor (VEGF) tyrosine kinase inhibitors (TKIs) and antibody-based therapies. Up to 58% of patients fail to respond to primary immune checkpoint inhibitor (ICI) therapy, and nearly all initial responders experience disease progression due to the development of secondary resistance. Consequently, novel treatment options are being investigated. Objective: Review the rapidly evolving ADC therapeutic landscape in metastatic RCC including recent trials, emerging ADCs targets, and future directions for ADCs in the treatment of advanced RCC. Methods: Literature review using the MEDLINE database on important trials and presentations from the American Society of Clinical Oncology (ASCO), and the European Society for Medical Oncology (ESMO) conferences. Key words used included “renal cell carcinoma,” “RCC,” “metastatic RCC,” “advanced RCC,” “antibody-based therapies,” “immunotherapy,” “clinical trials,” and “emerging drugs.” Specifically for review of ADCs in RCC, the following search string was used with additional review of bibliographies from retrieved papers: “((antibody drug conjugate) OR (antibody-dependent cellular cytotoxicity) OR (chimeric antigen receptor)) AND ((kidney cancer) OR (renal cell carcinoma))”. Results: Several promising targets including MMP14, EGFR, MCT4, CA9, MET, CDH13, B7-H3, and PSMA were identified with relevant preclinical and clinical studies reviewed. Conclusions: While ADCs therapeutics have not shown benefit to date for renal cell carcinoma, there are ample promising candidates and targets for future research.","PeriodicalId":17823,"journal":{"name":"Kidney Cancer","volume":" 6","pages":""},"PeriodicalIF":1.1000,"publicationDate":"2023-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kidney Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3233/kca-230012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Approximately 30% of renal cell carcinoma (RCC) cases present with de novo metastatic disease, while 20% to 30% of those with localized disease will develop metastases following surgical resection. Various drug classes have been investigated to treat RCC, including cytokine-based therapies, small molecule Vascular Endothelial Growth Factor (VEGF) tyrosine kinase inhibitors (TKIs) and antibody-based therapies. Up to 58% of patients fail to respond to primary immune checkpoint inhibitor (ICI) therapy, and nearly all initial responders experience disease progression due to the development of secondary resistance. Consequently, novel treatment options are being investigated. Objective: Review the rapidly evolving ADC therapeutic landscape in metastatic RCC including recent trials, emerging ADCs targets, and future directions for ADCs in the treatment of advanced RCC. Methods: Literature review using the MEDLINE database on important trials and presentations from the American Society of Clinical Oncology (ASCO), and the European Society for Medical Oncology (ESMO) conferences. Key words used included “renal cell carcinoma,” “RCC,” “metastatic RCC,” “advanced RCC,” “antibody-based therapies,” “immunotherapy,” “clinical trials,” and “emerging drugs.” Specifically for review of ADCs in RCC, the following search string was used with additional review of bibliographies from retrieved papers: “((antibody drug conjugate) OR (antibody-dependent cellular cytotoxicity) OR (chimeric antigen receptor)) AND ((kidney cancer) OR (renal cell carcinoma))”. Results: Several promising targets including MMP14, EGFR, MCT4, CA9, MET, CDH13, B7-H3, and PSMA were identified with relevant preclinical and clinical studies reviewed. Conclusions: While ADCs therapeutics have not shown benefit to date for renal cell carcinoma, there are ample promising candidates and targets for future research.
转移性肾细胞癌的新兴抗体药物共轭疗法和靶点
背景:约30%的肾细胞癌(RCC)病例会出现新的转移性疾病,而20%至30%的局部疾病患者在手术切除后会出现转移。治疗 RCC 的药物种类繁多,包括细胞因子疗法、小分子血管内皮生长因子(VEGF)酪氨酸激酶抑制剂(TKIs)和抗体疗法。多达58%的患者对免疫检查点抑制剂(ICI)的初治无效,几乎所有初治患者都会因继发耐药而导致疾病进展。因此,人们正在研究新的治疗方案。目的:回顾快速发展的 ADC 疗法:回顾快速发展的 ADC 治疗转移性 RCC 的情况,包括最近的试验、新出现的 ADCs 靶点以及 ADCs 治疗晚期 RCC 的未来方向。方法:使用 MEDLINE 数据库对美国临床肿瘤学会 (ASCO) 和欧洲肿瘤内科学会 (ESMO) 会议上的重要试验和报告进行文献综述。所用关键词包括 "肾细胞癌"、"RCC"、"转移性 RCC"、"晚期 RCC"、"抗体疗法"、"免疫疗法"、"临床试验 "和 "新兴药物"。具体到 ADC 在 RCC 中的应用,我们使用了以下搜索字符串,并对检索到的论文的参考书目进行了额外的审查:"((抗体药物共轭物)或(抗体依赖性细胞毒性)或(嵌合抗原受体))和((肾癌)或(肾细胞癌))"。结果:确定了几个有前景的靶点,包括 MMP14、表皮生长因子受体、MCT4、CA9、MET、CDH13、B7-H3 和 PSMA,并回顾了相关的临床前和临床研究。结论虽然 ADCs 疗法迄今尚未显示出对肾细胞癌的疗效,但仍有大量有希望的候选靶点可供未来研究使用。
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
Kidney Cancer
Kidney Cancer Multiple-
CiteScore
0.90
自引率
8.30%
发文量
23
×
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