转移性肾细胞癌一线治疗后的无治疗生存:一项国际转移性肾细胞癌数据库联盟分析。

IF 8.3 1区 医学 Q1 ONCOLOGY European urology oncology Pub Date : 2025-02-01 DOI:10.1016/j.euo.2024.12.011
Mehul Gupta , Connor Wells , Meredith M. Regan , Wanling Xie , Vishal Navani , Renee Maria Saliby , Naveen S. Basappa , Frede Donskov , Takeshi Yuasa , Kosuke Takemura , Christian K. Kollmannsberger , Megan Crumbaker , Aly-Khan A. Lalani , Thomas Powles , Hedyeh Ebrahimi , Rana R. McKay , Jae-Lyun Lee , Ravindran Kanesvaran , Toni K. Choueiri , Daniel Y.C. Heng
{"title":"转移性肾细胞癌一线治疗后的无治疗生存:一项国际转移性肾细胞癌数据库联盟分析。","authors":"Mehul Gupta ,&nbsp;Connor Wells ,&nbsp;Meredith M. Regan ,&nbsp;Wanling Xie ,&nbsp;Vishal Navani ,&nbsp;Renee Maria Saliby ,&nbsp;Naveen S. Basappa ,&nbsp;Frede Donskov ,&nbsp;Takeshi Yuasa ,&nbsp;Kosuke Takemura ,&nbsp;Christian K. Kollmannsberger ,&nbsp;Megan Crumbaker ,&nbsp;Aly-Khan A. Lalani ,&nbsp;Thomas Powles ,&nbsp;Hedyeh Ebrahimi ,&nbsp;Rana R. McKay ,&nbsp;Jae-Lyun Lee ,&nbsp;Ravindran Kanesvaran ,&nbsp;Toni K. Choueiri ,&nbsp;Daniel Y.C. Heng","doi":"10.1016/j.euo.2024.12.011","DOIUrl":null,"url":null,"abstract":"<div><h3>Background and objective</h3><div>Patients receiving immune checkpoint blockade (ICB) therapy may experience periods of prolonged disease control without a need for systemic therapy. Treatment-free survival (TFS) is an important measure for this period, but no data are available for patients with metastatic renal cell carcinoma (mRCC) starting first-line agents. Our aim was to analyze TFS outcomes for patients with mRCC starting first-line therapy.</div></div><div><h3>Methods</h3><div>We analyzed data for patients with mRCC starting first-line systemic therapy with VEGFR-targeted monotherapy, an ICB + VEGFR combination, or an ICB doublet from February 1, 2014 to February 1, 2023 from the multicenter International Metastatic RCC Database Consortium (IMDC) database. We estimated 36-mo TFS as the difference in restricted mean survival time between (1) the time to first-line therapy discontinuation and (2) the time to subsequent systemic therapy initiation.</div></div><div><h3>Key findings and limitations</h3><div>The study population included 3758 patients receiving either first-line VEGFR monotherapy (<em>n</em> = 2635), an ICB + VEGFR combination (<em>n</em> = 354), or doublet ICB (<em>n</em> = 769) were included. For the IMDC favorable-risk cohort, the 36-mo TFS estimate was 3.1 mo (95% confidence interval [CI] 1.5–4.6) for the VEGFR monotherapy group and 3.7 mo (95% CI 0.2–7.2) for the ICB + VEGFR group. For the IMDC intermediate-/poor-risk cohort, TFS was 2.1 mo (95% CI 1.4–2.8) for the VEGFR monotherapy group, 3.7 mo (95% CI 1.0–6.4) for the ICB + VEGFR group, and 5.3 mo (95% CI 3.8–6.8) for ICB doublet group. Limitations include the retrospective design and an inability to quantify time spent with adverse events.</div></div><div><h3>Conclusions and clinical implications</h3><div>Our study demonstrates that patients with IMDC intermediate or poor risk treated with ICB doublet therapy experienced longer TFS than those treated with VEGFR monotherapy in the first-line setting. These results emphasize the utility of TFS as an informative endpoint and provide survival estimates to inform decision-making in mRCC.</div></div><div><h3>Patient summary</h3><div>For patients with metastatic kidney cancer, we compared the survival time free from a second treatment line for different first-line treatment options. The results show that the time free from second-line treatment was longer when first-line treatment was with a combination of two immunotherapy drugs (ipilimumab and nivolumab) in comparison to other treatment options.</div></div>","PeriodicalId":12256,"journal":{"name":"European urology oncology","volume":"8 1","pages":"Pages 171-178"},"PeriodicalIF":8.3000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Treatment-free Survival After First-line Therapies for Metastatic Renal Cell Carcinoma: An International Metastatic Renal Cell Carcinoma Database Consortium Analysis\",\"authors\":\"Mehul Gupta ,&nbsp;Connor Wells ,&nbsp;Meredith M. Regan ,&nbsp;Wanling Xie ,&nbsp;Vishal Navani ,&nbsp;Renee Maria Saliby ,&nbsp;Naveen S. Basappa ,&nbsp;Frede Donskov ,&nbsp;Takeshi Yuasa ,&nbsp;Kosuke Takemura ,&nbsp;Christian K. Kollmannsberger ,&nbsp;Megan Crumbaker ,&nbsp;Aly-Khan A. Lalani ,&nbsp;Thomas Powles ,&nbsp;Hedyeh Ebrahimi ,&nbsp;Rana R. McKay ,&nbsp;Jae-Lyun Lee ,&nbsp;Ravindran Kanesvaran ,&nbsp;Toni K. Choueiri ,&nbsp;Daniel Y.C. Heng\",\"doi\":\"10.1016/j.euo.2024.12.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background and objective</h3><div>Patients receiving immune checkpoint blockade (ICB) therapy may experience periods of prolonged disease control without a need for systemic therapy. Treatment-free survival (TFS) is an important measure for this period, but no data are available for patients with metastatic renal cell carcinoma (mRCC) starting first-line agents. Our aim was to analyze TFS outcomes for patients with mRCC starting first-line therapy.</div></div><div><h3>Methods</h3><div>We analyzed data for patients with mRCC starting first-line systemic therapy with VEGFR-targeted monotherapy, an ICB + VEGFR combination, or an ICB doublet from February 1, 2014 to February 1, 2023 from the multicenter International Metastatic RCC Database Consortium (IMDC) database. We estimated 36-mo TFS as the difference in restricted mean survival time between (1) the time to first-line therapy discontinuation and (2) the time to subsequent systemic therapy initiation.</div></div><div><h3>Key findings and limitations</h3><div>The study population included 3758 patients receiving either first-line VEGFR monotherapy (<em>n</em> = 2635), an ICB + VEGFR combination (<em>n</em> = 354), or doublet ICB (<em>n</em> = 769) were included. For the IMDC favorable-risk cohort, the 36-mo TFS estimate was 3.1 mo (95% confidence interval [CI] 1.5–4.6) for the VEGFR monotherapy group and 3.7 mo (95% CI 0.2–7.2) for the ICB + VEGFR group. For the IMDC intermediate-/poor-risk cohort, TFS was 2.1 mo (95% CI 1.4–2.8) for the VEGFR monotherapy group, 3.7 mo (95% CI 1.0–6.4) for the ICB + VEGFR group, and 5.3 mo (95% CI 3.8–6.8) for ICB doublet group. Limitations include the retrospective design and an inability to quantify time spent with adverse events.</div></div><div><h3>Conclusions and clinical implications</h3><div>Our study demonstrates that patients with IMDC intermediate or poor risk treated with ICB doublet therapy experienced longer TFS than those treated with VEGFR monotherapy in the first-line setting. These results emphasize the utility of TFS as an informative endpoint and provide survival estimates to inform decision-making in mRCC.</div></div><div><h3>Patient summary</h3><div>For patients with metastatic kidney cancer, we compared the survival time free from a second treatment line for different first-line treatment options. The results show that the time free from second-line treatment was longer when first-line treatment was with a combination of two immunotherapy drugs (ipilimumab and nivolumab) in comparison to other treatment options.</div></div>\",\"PeriodicalId\":12256,\"journal\":{\"name\":\"European urology oncology\",\"volume\":\"8 1\",\"pages\":\"Pages 171-178\"},\"PeriodicalIF\":8.3000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European urology oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2588931124002931\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European urology oncology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2588931124002931","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景和目的:接受免疫检查点阻断(ICB)治疗的患者可能会经历一段较长时间的疾病控制,而不需要全身治疗。无治疗生存期(TFS)是这一时期的重要指标,但没有关于转移性肾细胞癌(mRCC)患者起始一线药物的数据。我们的目的是分析mRCC患者开始一线治疗的TFS结果。方法:我们分析了2014年2月1日至2023年2月1日来自多中心国际转移性RCC数据库联盟(IMDC)数据库的mRCC患者的数据,这些患者开始接受一线全身治疗,包括VEGFR靶向单药治疗、ICB + VEGFR联合治疗或ICB双药治疗。我们估计36个月的TFS是(1)到一线治疗停止的时间和(2)到随后的全身治疗开始的时间之间的限制平均生存时间的差异。主要发现和局限性:研究人群包括3758名接受一线VEGFR单药治疗(n = 2635)、ICB + VEGFR联合治疗(n = 354)或ICB双药治疗(n = 769)的患者。对于IMDC有利风险队列,VEGFR单药组的36个月TFS估计为3.1个月(95%置信区间[CI] 1.5-4.6), ICB + VEGFR组的36个月TFS估计为3.7个月(95%置信区间[CI] 0.2-7.2)。对于IMDC中/低风险队列,VEGFR单药组的TFS为2.1个月(95% CI 1.4-2.8), ICB + VEGFR组的TFS为3.7个月(95% CI 1.0-6.4), ICB双药组的TFS为5.3个月(95% CI 3.8-6.8)。局限性包括回顾性设计和无法量化不良事件所花费的时间。结论和临床意义:我们的研究表明,在一线环境中,接受ICB双药治疗的中度或低风险IMDC患者的TFS比接受VEGFR单药治疗的患者更长。这些结果强调了TFS作为信息终点的效用,并为mRCC的决策提供了生存估计。患者总结:对于转移性肾癌患者,我们比较了不同一线治疗方案的第二治疗线的生存时间。结果显示,与其他治疗方案相比,一线治疗联合使用两种免疫治疗药物(ipilimumab和nivolumab)时,脱离二线治疗的时间更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Treatment-free Survival After First-line Therapies for Metastatic Renal Cell Carcinoma: An International Metastatic Renal Cell Carcinoma Database Consortium Analysis

Background and objective

Patients receiving immune checkpoint blockade (ICB) therapy may experience periods of prolonged disease control without a need for systemic therapy. Treatment-free survival (TFS) is an important measure for this period, but no data are available for patients with metastatic renal cell carcinoma (mRCC) starting first-line agents. Our aim was to analyze TFS outcomes for patients with mRCC starting first-line therapy.

Methods

We analyzed data for patients with mRCC starting first-line systemic therapy with VEGFR-targeted monotherapy, an ICB + VEGFR combination, or an ICB doublet from February 1, 2014 to February 1, 2023 from the multicenter International Metastatic RCC Database Consortium (IMDC) database. We estimated 36-mo TFS as the difference in restricted mean survival time between (1) the time to first-line therapy discontinuation and (2) the time to subsequent systemic therapy initiation.

Key findings and limitations

The study population included 3758 patients receiving either first-line VEGFR monotherapy (n = 2635), an ICB + VEGFR combination (n = 354), or doublet ICB (n = 769) were included. For the IMDC favorable-risk cohort, the 36-mo TFS estimate was 3.1 mo (95% confidence interval [CI] 1.5–4.6) for the VEGFR monotherapy group and 3.7 mo (95% CI 0.2–7.2) for the ICB + VEGFR group. For the IMDC intermediate-/poor-risk cohort, TFS was 2.1 mo (95% CI 1.4–2.8) for the VEGFR monotherapy group, 3.7 mo (95% CI 1.0–6.4) for the ICB + VEGFR group, and 5.3 mo (95% CI 3.8–6.8) for ICB doublet group. Limitations include the retrospective design and an inability to quantify time spent with adverse events.

Conclusions and clinical implications

Our study demonstrates that patients with IMDC intermediate or poor risk treated with ICB doublet therapy experienced longer TFS than those treated with VEGFR monotherapy in the first-line setting. These results emphasize the utility of TFS as an informative endpoint and provide survival estimates to inform decision-making in mRCC.

Patient summary

For patients with metastatic kidney cancer, we compared the survival time free from a second treatment line for different first-line treatment options. The results show that the time free from second-line treatment was longer when first-line treatment was with a combination of two immunotherapy drugs (ipilimumab and nivolumab) in comparison to other treatment options.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
期刊最新文献
Comparative Performance of Machine Learning Models in Reducing Unnecessary Targeted Prostate Biopsies. Towards a Consensus on the Management of Metastatic Renal Cell Carcinoma: Insights from a European Delphi Study. Re: Bertrand F. Tombal, Francisco Gomez-Veiga, Alvaro Gomez-Ferrer, et al. A Phase 2 Randomized Open-label Study of Oral Darolutamide Monotherapy Versus Androgen Deprivation Therapy in Men with Hormone-sensitive Prostate Cancer (EORTC-GUCG 1532). Eur Urol Oncol 2024;7:1051-60. Results of Stereotactic Body Radiation Therapy for Primary Renal Cell Carcinoma in a Large Multicenter Series. Association of Prior PARP Inhibitor Exposure with Clinical Outcomes after 177Lu-PSMA-617 in Men with Castration-resistant Prostate Cancer and Mutations in DNA Homologous Recombination Repair Genes.
×
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