Real-World Outcomes of Nivolumab Plus Ipilimumab Versus Pembrolizumab Plus Axitinib for First-Line Treatment of Advanced Renal Cell Carcinoma

IF 2.4 3区 医学 Q3 ONCOLOGY
Clinical genitourinary cancer Pub Date : 2025-12-01 Epub Date: 2025-09-25 DOI:10.1016/j.clgc.2025.102443
Daniel M. Geynisman , William S. John , Taavy A. Miller , Parisa Asgarisabet , Angelica Falkenstein , Kristin M. Zimmerman Savill , Xin Yin , Viviana del Tejo , Sarah B. Guttenplan , Lisa Rosenblatt
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引用次数: 0

Abstract

Background

In the absence of head-to-head trials, real-world (RW) outcomes of patients with advanced renal cell carcinoma (aRCC) treated with immuno-oncology combinations are important for clinicians and patients. Here, we describe treatment patterns, adverse events (AEs), and outcomes of patients with aRCC treated with first-line (1L) nivolumab plus ipilimumab (NIVO+IPI) or pembrolizumab plus axitinib (PEM+AXI).

Methods

This retrospective medical chart review included patients with aRCC who initiated 1L NIVO+IPI between May-2018 and May-2021 or PEM+AXI between May-2019 and May-2021. Inverse probability of treatment weighting was performed, providing balanced baseline characteristics. Physician-reported response (RW objective response rate [rwORR], duration of response [rwDOR]) and immune-related AEs are described. RW progression-free survival (rwPFS) and overall survival (rwOS) were estimated using Kaplan-Meier analysis.

Results

225 patients were treated with 1L NIVO+IPI and 130 with 1L PEM+AXI. The median duration of 1L therapy was 15.0 months for NIVO+IPI and 14.5 months for PEM+AXI. After weighting, each cohort was ∼60% male, ∼65 years old, and ∼90% had intermediate/poor risk scores at initiation. The median follow-up post-1L initiation was 22.4 months for NIVO+IPI and 19.0 months for PEM+AXI (P = .006). The rwORR was comparable between cohorts (NIVO+IPI, 71.5%; PEM+AXI, 77.3%; P = .24), whereas the median rwDOR was significantly longer in the NIVO+IPI versus the PEM+AXI cohort (11.0 vs. 8.0 months; P < .0001). While median rwPFS and rwOS did not differ by treatment (P = .20 and 0.37, respectively), estimates for rwPFS and rwOS probability at 24 months post-1L initiation for treatment were nonsignificantly higher for NIVO+IPI versus PEM+AXI (rwPFS: 0.29 vs. 0.18, respectively; rwOS: 0.63 vs. 0.57, respectively). The overall rate of immune-related AEs was similar between cohorts (NIVO+IPI, 29.1%; PEM+AXI, 25.3%; significance not tested).

Conclusions

Overall results from this RW study were similar for patients with aRCC who received 1L NIVO+IPI or PEM+AXI, although nonsignificant results suggest rwPFS and rwOS at later timepoints may be improved for patients who receive 1L NIVO+IPI versus PEM+AXI. Additional research with larger samples and extended follow-up is necessary to understand potential long-term differences in clinical outcomes.
Nivolumab + Ipilimumab与Pembrolizumab + Axitinib一线治疗晚期肾细胞癌的实际结果
背景:在缺乏头对头试验的情况下,晚期肾细胞癌(aRCC)患者接受免疫肿瘤联合治疗的真实世界(RW)结果对临床医生和患者都很重要。在这里,我们描述了治疗模式、不良事件(ae)和aRCC患者接受一线(1L)尼沃单抗加伊匹单抗(NIVO+IPI)或派姆单抗加阿西替尼(PEM+AXI)治疗的结果。方法:本回顾性病历回顾包括2018年5月至2021年5月间接受1L NIVO+IPI治疗或2019年5月至2021年5月间接受PEM+AXI治疗的aRCC患者。进行治疗加权的逆概率,提供平衡的基线特征。描述了医生报告的反应(客观反应率[rwORR],反应持续时间[rwDOR])和免疫相关的ae。采用Kaplan-Meier分析估计RW无进展生存期(rwPFS)和总生存期(rwOS)。结果:225例患者采用1L NIVO+IPI, 130例患者采用1L PEM+AXI。NIVO+IPI的1L治疗中位持续时间为15.0个月,PEM+AXI的中位持续时间为14.5个月。加权后,每个队列约60%为男性,约65岁,约90%在开始时具有中等/较差的风险评分。NIVO+IPI的1l起始后中位随访时间为22.4个月,PEM+AXI的19.0个月(P = 0.006)。队列之间的rwORR具有可比性(NIVO+IPI, 71.5%; PEM+AXI, 77.3%; P = 0.24),而NIVO+IPI组的中位rwDOR明显长于PEM+AXI组(11.0个月vs 8.0个月;P < 0.0001)。虽然中位rwPFS和rwOS没有因治疗而差异(分别为P = 0.20和0.37),但NIVO+IPI与PEM+AXI治疗后24个月的rwPFS和rwOS概率估计值无显著性升高(rwPFS分别为0.29和0.18;rwOS分别为0.63和0.57)。免疫相关不良事件的总体发生率在队列之间相似(NIVO+IPI, 29.1%; PEM+AXI, 25.3%;未检验显著性)。结论:RW研究的总体结果与接受1L NIVO+IPI或PEM+AXI的aRCC患者相似,尽管不显著的结果表明,接受1L NIVO+IPI的患者在较晚时间点的rwPFS和rwOS可能比接受PEM+AXI的患者有所改善。为了了解临床结果的潜在长期差异,有必要进行更大样本和更长时间随访的进一步研究。
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来源期刊
Clinical genitourinary cancer
Clinical genitourinary cancer 医学-泌尿学与肾脏学
CiteScore
5.20
自引率
6.20%
发文量
201
审稿时长
54 days
期刊介绍: Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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