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
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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. 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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。
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.
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