Urabe Fumihiko, Tashiro Kojiro, Imai Yu, Iwatani Kosuke, Uchida Naoki, Taneda Yuki, Shibata Ken, Hashimoto Masaki, Kawano Shota, Takiguchi Yuki, Ohtsuka Takashi, Nakazono Minoru, Kayano Sotaro, Atsuta Mahito, Murakami Masaya, Tsuzuki Shunsuke, Yamamoto Toshihiro, Yamada Hiroki, Miki Jun, Kimura Takahiro
Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Department of Urology, Jikei the 3rd Hospital, Tokyo, Japan.
Int J Urol. 2025 Sep;32(9):1147-1156. doi: 10.1111/iju.70113. Epub 2025 May 15.
Few studies have provided a comprehensive analysis of sequential treatment strategies for locally advanced and metastatic urothelial carcinoma (la/mUC). This study assessed treatment patterns, prognostic factors, and optimal sequencing strategies in patients receiving first-line platinum-based chemotherapy (1 L-PBC).
This retrospective, multicenter study analyzed 212 la/mUC patients who initiated 1 L-PBC. Treatment sequences were categorized based on the therapy, including immune-oncology (IO) drug and enfortumab vedotin (EV) therapy. Multivariate logistic regression identified risk factors for failing to progress to EV therapy.
The median follow-up duration was 17 months. Of the 212 patients, 65 (38.9%) progressed to EV therapy, achieving the longest median overall survival (OS) of 41 months, compared to 25 months in the 1 L-PBC + IO group and 8 months in the 1 L-PBC group. Poor performance status (ECOG-PS ≥ 1), age ≥ 80 years, and elevated levels of C-reactive protein (≥ 1) were significant predictors of failing to reach EV therapy. Kaplan-Meier analysis indicated no survival difference based on avelumab use in patients with no risk factors, but patients with one or more risk factors receiving avelumab had significantly longer OS than patients who did not receive avelumab.
This study emphasizes the prognostic importance of achieving EV therapy and the role of maintenance avelumab in improving outcomes for la/mUC patients with one or more risk factors after 1 L-PBC. Combining EV with pembrolizumab is a promising first-line treatment, and 1 L-PBC remains a viable option for selected patients.
很少有研究对局部晚期和转移性尿路上皮癌(la/mUC)的序贯治疗策略进行全面分析。本研究评估了接受一线铂类化疗(1L-PBC)患者的治疗模式、预后因素和最佳序贯策略。
这项回顾性多中心研究分析了212例开始接受1L-PBC治疗的la/mUC患者。根据治疗方法对治疗顺序进行分类,包括免疫肿瘤(IO)药物和恩扎妥昔单抗(EV)治疗。多变量逻辑回归确定了未能进展至EV治疗的危险因素。
中位随访时间为17个月。在212例患者中,65例(38.9%)进展至EV治疗,中位总生存期(OS)最长达41个月,相比之下,1L-PBC + IO组为25个月,1L-PBC组为8个月。体能状态差(东部肿瘤协作组体能状态评分≥1)、年龄≥80岁和C反应蛋白水平升高(≥1)是未能接受EV治疗的显著预测因素。Kaplan-Meier分析表明,无危险因素的患者使用阿维鲁单抗与否在生存方面无差异,但有一个或多个危险因素且接受阿维鲁单抗治疗的患者OS明显长于未接受阿维鲁单抗治疗的患者。
本研究强调了接受EV治疗的预后重要性以及维持使用阿维鲁单抗在改善1L-PBC后有一个或多个危险因素的la/mUC患者结局中的作用。将EV与派姆单抗联合使用是一种有前景的一线治疗方法,1L-PBC对特定患者仍是一个可行的选择。