First-line Enfortumab Vedotin Plus Pembrolizumab in Platinum-ineligible Advanced Urothelial Carcinoma.

G O Kaneko, Daisuke Igarashi, Suguru Shirotake
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Abstract

Background/aim: Platinum-ineligible patients with locally advanced or metastatic urothelial carcinoma represent a clinically vulnerable population with limited treatment options and poor historical outcomes. Although first-line enfortumab vedotin plus pembrolizumab has become a new standard treatment, evidence in platinum-ineligible patients remains limited. This study described the real-world clinical course of platinum-ineligible patients treated with first-line enfortumab vedotin plus pembrolizumab within a consecutive cohort.

Patients and methods: This retrospective single-center study included 40 consecutive patients with locally advanced or metastatic urothelial carcinoma who initiated first-line enfortumab vedotin plus pembrolizumab between December 2024 and March 2026. Platinum eligibility was determined using prespecified creatinine clearance-based criteria. Tumor response, progression-free survival, overall survival, treatment-related adverse events, and individual treatment courses were evaluated descriptively.

Results: Among 40 patients, eight were classified as platinum ineligible. Tumor response was evaluable in six platinum-ineligible patients, of whom one achieved complete response and three achieved partial response. Median progression-free survival and overall survival were not reached in the platinum-ineligible subgroup. Grade ≥3 treatment-related adverse events were infrequent. The swimmer plot demonstrated heterogeneous clinical trajectories, including early discontinuation in some patients and prolonged treatment exposure or off-treatment disease control in others.

Conclusion: First-line enfortumab vedotin plus pembrolizumab showed encouraging clinical activity and acceptable tolerability in selected platinum-ineligible patients with advanced urothelial carcinoma. Given the small subgroup size, these findings should be interpreted as descriptive and hypothesis-generating.

一线Enfortumab Vedotin + Pembrolizumab治疗铂不合格晚期尿路上皮癌
背景/目的:不适合铂治疗的局部晚期或转移性尿路上皮癌患者是临床易感人群,治疗选择有限,历史预后不良。尽管一线的维多汀+派姆单抗已成为新的标准治疗,但在铂不合格患者中的证据仍然有限。该研究描述了连续队列中接受一线维多汀+派姆单抗治疗的铂不合格患者的真实临床过程。患者和方法:这项回顾性单中心研究纳入了40例连续的局部晚期或转移性尿路上皮癌患者,这些患者在2024年12月至2026年3月期间接受了一线维多汀+派姆单抗的治疗。使用预先指定的肌酐清除率标准确定铂金资格。描述性地评估肿瘤反应、无进展生存期、总生存期、治疗相关不良事件和个体治疗疗程。结果:40例患者中,8例为铂不合格。6例铂不合格患者的肿瘤反应可评估,其中1例达到完全缓解,3例达到部分缓解。在铂不合格亚组中,中位无进展生存期和总生存期未达到。≥3级治疗相关不良事件很少发生。游泳者图显示了不同的临床轨迹,包括一些患者早期停药,另一些患者延长治疗暴露或停止治疗疾病控制。结论:在选定的铂不合格晚期尿路上皮癌患者中,一线enfortumab vedotin联合派姆单抗显示出令人鼓舞的临床活性和可接受的耐受性。考虑到小的亚组规模,这些发现应该被解释为描述性和假设生成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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