Trastuzumab deruxtecan: An antibody-drug conjugates for non-small cell lung cancer.

IF 0.9 4区 医学 Q4 ONCOLOGY
Nahida Siddiqui, Gojuvaka Sravanthi, Kanugonda Jashwanth Kumar Reddy, Kummarikunta Salomi, Tadikonda Rama Rao, V V Rajesham
{"title":"Trastuzumab deruxtecan: An antibody-drug conjugates for non-small cell lung cancer.","authors":"Nahida Siddiqui, Gojuvaka Sravanthi, Kanugonda Jashwanth Kumar Reddy, Kummarikunta Salomi, Tadikonda Rama Rao, V V Rajesham","doi":"10.1177/10781552251383762","DOIUrl":null,"url":null,"abstract":"<p><p>ObjectivesThis review compiles to provide an overview of non-small cell lung cancer (NSCLC) and the therapeutic rationale for antibody-drug conjugates (ADCs), followed by a summary of current evidence highlighting the efficacy, safety, and adverse event management of trastuzumab deruxtecan (T-DXd) in HER2-mutant metastatic NSCLC.Data SourcePUBMED, ClinicalTrials.gov, and Google Scholar were searched to retrieve relevant clinical studies including randomized controlled trials, non-randomized studies, observational studies, and real-world evidence from its approval to July, 2025 for the treatment of patients with HER2-mutant metastatic NSCLC received prior systemic therapy. The search strategy was guided by the target therapeutic area, intervention type, and population studied.Data SummaryT-DXd, a HER2-targeted ADC and second line treatment, has shown significant clinical benefit in HER2-mutant metastatic NSCLC, as evidenced by key clinical trials (NCT04644237 and NCT04644237) demonstrating high objective response rates (ORRs) and disease control rates (DCRs). Although it exhibits a manageable safety profile, interstitial lung disease (ILD) remains a notable adverse event (AE), with improved tolerability observed at the lower dose of 5.4 mg/kg. Moreover, multidisciplinary Strategies are also used to manage T-DXd associated AEs. Additionally, ongoing trials are evaluating the combination of T-DXd with immunotherapy and targeted agents to optimize safety outcomes and efficacy in high-risk NSCLC populations.ConclusionsT-DXd at 5.4 mg/kg offers substantial efficacy with better tolerability than 6.4 mg/kg. Incorporating AE mitigation, real-world insights, and combination trial data may further optimize its safety and clinical benefit in this biomarker-defined population.</p>","PeriodicalId":16637,"journal":{"name":"Journal of Oncology Pharmacy Practice","volume":" ","pages":"10781552251383762"},"PeriodicalIF":0.9000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oncology Pharmacy Practice","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/10781552251383762","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

ObjectivesThis review compiles to provide an overview of non-small cell lung cancer (NSCLC) and the therapeutic rationale for antibody-drug conjugates (ADCs), followed by a summary of current evidence highlighting the efficacy, safety, and adverse event management of trastuzumab deruxtecan (T-DXd) in HER2-mutant metastatic NSCLC.Data SourcePUBMED, ClinicalTrials.gov, and Google Scholar were searched to retrieve relevant clinical studies including randomized controlled trials, non-randomized studies, observational studies, and real-world evidence from its approval to July, 2025 for the treatment of patients with HER2-mutant metastatic NSCLC received prior systemic therapy. The search strategy was guided by the target therapeutic area, intervention type, and population studied.Data SummaryT-DXd, a HER2-targeted ADC and second line treatment, has shown significant clinical benefit in HER2-mutant metastatic NSCLC, as evidenced by key clinical trials (NCT04644237 and NCT04644237) demonstrating high objective response rates (ORRs) and disease control rates (DCRs). Although it exhibits a manageable safety profile, interstitial lung disease (ILD) remains a notable adverse event (AE), with improved tolerability observed at the lower dose of 5.4 mg/kg. Moreover, multidisciplinary Strategies are also used to manage T-DXd associated AEs. Additionally, ongoing trials are evaluating the combination of T-DXd with immunotherapy and targeted agents to optimize safety outcomes and efficacy in high-risk NSCLC populations.ConclusionsT-DXd at 5.4 mg/kg offers substantial efficacy with better tolerability than 6.4 mg/kg. Incorporating AE mitigation, real-world insights, and combination trial data may further optimize its safety and clinical benefit in this biomarker-defined population.

曲妥珠单抗德鲁西替康:非小细胞肺癌的抗体-药物偶联物。
本综述综述了非小细胞肺癌(NSCLC)和抗体-药物偶联物(adc)的治疗原理,随后总结了当前证据,强调了曲妥珠单抗德鲁德康(T-DXd)在her2突变转移性NSCLC中的有效性、安全性和不良事件管理。数据来源检索pubmed、ClinicalTrials.gov和谷歌Scholar,检索从批准到2025年7月的相关临床研究,包括随机对照试验、非随机研究、观察性研究和真实证据,用于治疗先前接受全身治疗的her2突变转移性NSCLC患者。搜索策略以目标治疗区域、干预类型和研究人群为指导。关键临床试验(NCT04644237和NCT04644237)证明,t - dxd是一种her2靶向ADC和二线治疗,在her2突变的转移性NSCLC中显示出显着的临床益处,显示出较高的客观缓解率(ORRs)和疾病控制率(dcr)。虽然它具有可控的安全性,但间质性肺疾病(ILD)仍然是一个显著的不良事件(AE),在较低剂量5.4 mg/kg时观察到耐受性改善。此外,多学科策略也用于管理T-DXd相关的ae。此外,正在进行的试验正在评估T-DXd与免疫疗法和靶向药物的联合使用,以优化高危NSCLC人群的安全性、预后和疗效。结论5.4 mg/kg剂量的st - dxd疗效显著,耐受性优于6.4 mg/kg剂量。结合AE缓解、现实世界的见解和联合试验数据,可以进一步优化其在生物标志物定义的人群中的安全性和临床益处。
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
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
×
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:604180095
Book学术官方微信