Morikawa Toshiharu, Naiki Taku, Sugiyama Yosuke, Naiki-Ito Aya, Nagai Takashi, Etani Toshiki, Iida Keitaro, Isobe Teruki, Noda Yusuke, Shimizu Nobuhiko, Aoki Maria, Gonda Masakazu, Banno Rika, Kubota Hiroki, Ando Ryosuke, Umemoto Yukihiro, Kawai Noriyasu, Yasui Takahiro
Department of Nephro-Urology, Graduate School of Medical Sciences, Nagoya City University, Nagoya 467-8601, Japan.
Department of Urology, Nagoya City University West Medical Center, Nagoya 467-8601, Japan.
Cancers (Basel). 2024 Apr 28;16(9):1725. doi: 10.3390/cancers16091725.
In the EV-301 trial, enfortumab vedotin prolonged survival in patients with locally advanced or metastatic urothelial carcinoma previously treated with platinum-based therapy and programmed cell death 1/programmed death-ligand 1 inhibitor. However, real-world Asian data are limited, and potential prognostic markers are non-existent. We aimed to investigate potential prognostic markers for enfortumab vedotin therapy in Asian patients.
We retrospectively enrolled 61 Japanese patients treated with enfortumab vedotin therapy at our hospital and affiliated hospitals between January 2019 and September 2023.
Enrolled patients (38 men, 23 women; median age 74 [IQR: 68-79] years) had bladder cancer (26 patients) or upper-tract urothelial carcinoma (35 patients). Fifty-four patients reported adverse events (grade >3 in 12). Skin disorders, pruritus, and neuropathy were common adverse effects. The median overall survival was 17.1 months (95% confidence interval: 10.0-not applicable). In multivariate analysis, the C-reactive protein level was an independent marker predicting favorable overall survival with enfortumab vedotin. Patient characteristics did not differ between C-reactive protein-high and -low groups.
Our study provides real-world data showing that enfortumab vedotin prolonged survival in Asian patients similar to the EV-301 trial. Additionally, the C-reactive protein level might be considered a prognostic marker of enfortumab vedotin therapy in such patients.
在EV-301试验中,恩杂鲁胺延长了先前接受铂类疗法和程序性细胞死亡1/程序性死亡配体1抑制剂治疗的局部晚期或转移性尿路上皮癌患者的生存期。然而,真实世界的亚洲数据有限,且不存在潜在的预后标志物。我们旨在研究亚洲患者接受恩杂鲁胺治疗的潜在预后标志物。
我们回顾性纳入了2019年1月至2023年9月期间在我院及附属医院接受恩杂鲁胺治疗的61例日本患者。
入组患者(38例男性,23例女性;中位年龄74岁[四分位间距:68-79岁])患有膀胱癌(26例患者)或上尿路尿路上皮癌(35例患者)。54例患者报告了不良事件(12例为3级以上)。皮肤疾病、瘙痒和神经病变是常见的不良反应。中位总生存期为17.1个月(95%置信区间:10.0-不可用)。在多变量分析中,C反应蛋白水平是预测恩杂鲁胺治疗总体生存期良好的独立标志物。C反应蛋白高和低的组间患者特征无差异。
我们的研究提供了真实世界的数据,表明恩杂鲁胺在亚洲患者中延长生存期的情况与EV-301试验相似。此外,C反应蛋白水平可能被视为这类患者接受恩杂鲁胺治疗的预后标志物。