Uchimoto Taizo, Iwatsuki Kengo, Komura Kazumasa, Fukuokaya Wataru, Adachi Takahiro, Hirasawa Yosuke, Hashimoto Takeshi, Yoshizawa Atsuhiko, Saruta Masanobu, Hashimoto Mamoru, Minami Takafumi, Yamamoto Yutaka, Yamazaki Shogo, Takai Tomoaki, Sakamoto Moritoshi, Nakajima Yuki, Nishimura Kazuki, Maenosono Ryoichi, Tsujino Takuya, Nakamura Ko, Fukushima Tatsuo, Nishio Kyosuke, Yoshikawa Yuki, Yamamoto Shutaro, Iwatani Kosuke, Urabe Fumihiko, Mori Keiichiro, Yanagisawa Takafumi, Tsuduki Shunsuke, Takahara Kiyoshi, Fujita Kazutoshi, Kimura Takahiro, Ohno Yoshio, Shiroki Ryoichi, Azuma Haruhito
Department of Urology, Osaka Medical and Pharmaceutical University, 2-7 Daigaku-Machi, Takatsuki City, Osaka, 569-8686, Japan.
Department of Urology, The Jikei University School of Medicine, 3-25-8, Nishi-shimbashi, Minato-ku, Tokyo, 105-8461, Japan.
Int J Clin Oncol. 2025 Apr;30(4):761-769. doi: 10.1007/s10147-025-02709-1. Epub 2025 Jan 31.
Enfortumab vedotin (EV), an antibody-drug conjugate (ADC) targeting Nectin-4, has been available as standard care for metastatic urothelial carcinoma (mUC) patients who have progressed after platinum-based chemotherapy and checkpoint inhibitors (CPIs). However, the association between body mass index (BMI) and clinical outcomes for EV remains unknown.
We analyzed the records of 123 mUC patients who received EV. The cohort was divided into low BMI (< 22, n = 65) and high BMI (≥ 22, n = 58) groups. Propensity score matching was performed to reduce clinical bias between the two groups.
In the total cohort (n = 123), the objective response rate (ORR) and disease control rate (DCR) were 46% and 68%, respectively. The ORR was significantly higher in the higher BMI group (62%, n = 58) compared to the lower BMI group (32%, n = 65). Among the pair-matched cohort (n = 100), despite reducing potential bias, the ORR remained significantly higher in the higher BMI group than in the lower BMI group (64% vs. 32%, p = 0.002). Both overall survival (OS) and radiographic progression-free survival (r-PFS) were longer in the higher BMI group compared to the lower BMI group (median OS: not reached vs. 8 months, p = 0.035; median r-PFS: 10 vs. 4 months, p < 0.001). On multivariate analyses, a higher BMI (≥ 22) was an independent predictor for achieving objective response and favorable OS in mUC patients treated with EV.
The findings of this study suggest a potential association between high BMI and improved tumor response to EV in mUC patients with disease progression after platinum-based chemotherapy and CPIs.
恩沃利单抗(EV)是一种靶向Nectin-4的抗体药物偶联物(ADC),已作为铂类化疗和检查点抑制剂(CPI)治疗后进展的转移性尿路上皮癌(mUC)患者的标准治疗药物。然而,体重指数(BMI)与EV临床结局之间的关联尚不清楚。
我们分析了123例接受EV治疗的mUC患者的记录。该队列分为低BMI组(<22,n = 65)和高BMI组(≥22,n = 58)。进行倾向评分匹配以减少两组之间的临床偏倚。
在整个队列(n = 123)中,客观缓解率(ORR)和疾病控制率(DCR)分别为46%和68%。高BMI组(n = 58)的ORR显著高于低BMI组(n = 65)(62% vs 32%)。在配对匹配队列(n = 100)中,尽管减少了潜在偏倚,但高BMI组的ORR仍显著高于低BMI组(64% vs 32%,p = 0.002)。高BMI组的总生存期(OS)和影像学无进展生存期(r-PFS)均长于低BMI组(中位OS:未达到 vs 8个月,p = 0.035;中位r-PFS:10个月 vs 4个月,p < 0.001)。多因素分析显示,较高的BMI(≥22)是接受EV治疗的mUC患者实现客观缓解和良好OS的独立预测因素。
本研究结果表明,在铂类化疗和CPI治疗后疾病进展的mUC患者中,高BMI与肿瘤对EV的反应改善之间可能存在关联。