Department of Medical Oncology, The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Osaka University Hospital, Osaka, Japan.
Invest New Drugs. 2020 Aug;38(4):1056-1066. doi: 10.1007/s10637-019-00844-x. Epub 2019 Aug 14.
Locally advanced or metastatic urothelial cancer is an aggressive form of cancer with high recurrence rates and low survival. Nectin-4 is a cell adhesion molecule commonly expressed in several tumors, including high expression in urothelial cancer. Enfortumab vedotin is an antibody-drug conjugate composed of an anti-Nectin-4 humanized monoclonal antibody linked to the microtubule disrupting agent, monomethyl auristatin E. In this phase I study (NCT03070990), Japanese patients with locally advanced/metastatic urothelial cancer treated with prior chemotherapy, or ineligible for cisplatin, were randomized 1:1 to receive 1.0 mg/kg (Arm A) or 1.25 mg/kg (Arm B) enfortumab vedotin on Days 1, 8, and 15 of each 28-day cycle. Assessing the pharmacokinetic and safety/tolerability profiles of enfortumab vedotin were primary objectives; investigator-assessed antitumor activity (RECIST v1.1) was a secondary objective. Seventeen patients (n = 9, Arm A; n = 8, Arm B) received treatment. Pharmacokinetic data suggest a dose-dependent increase in enfortumab vedotin maximum concentration and area under the concentration-time curve at Day 7. Enfortumab vedotin was well tolerated across both doses. Dysgeusia and alopecia (n = 9 each) were the most common treatment-related adverse events. Regardless of attribution, grade ≥ 3 adverse events occurring in ≥2 patients were anemia and hypertension (n = 2 each). One patient achieved a confirmed complete response (Arm A) and five achieved confirmed partial responses (n = 3, Arm A; n = 2, Arm B). Objective response and disease control rates were 35.3% and 76.5%, respectively. In Japanese patients with locally advanced/metastatic urothelial cancer, enfortumab vedotin is well tolerated with preliminary antitumor activity and a pharmacokinetic profile consistent with prior reports.
局部晚期或转移性尿路上皮癌是一种侵袭性癌症,复发率高,生存率低。Nectin-4 是一种细胞黏附分子,在几种肿瘤中均有高表达,包括尿路上皮癌。Enfortumab vedotin 是一种抗体药物偶联物,由与人 Nectin-4 结合的单克隆抗体和微管破坏剂单甲基澳瑞他汀 E 组成。在这项 I 期研究(NCT03070990)中,先前接受过化疗或不适合顺铂治疗的局部晚期/转移性尿路上皮癌日本患者,按 1:1 随机分配接受 1.0mg/kg(A 组)或 1.25mg/kg(B 组)enfortumab vedotin,每 28 天周期的第 1、8 和 15 天给药。评估 enfortumab vedotin 的药代动力学和安全性/耐受性特征是主要目标;研究者评估的抗肿瘤活性(RECIST v1.1)是次要目标。17 名患者(n=9,A 组;n=8,B 组)接受了治疗。药代动力学数据表明,在第 7 天,enfortumab vedotin 的最大浓度和浓度-时间曲线下面积呈剂量依赖性增加。两种剂量下的 enfortumab vedotin 均具有良好的耐受性。味觉障碍和脱发(n=9)是最常见的与治疗相关的不良事件。无论归因如何,发生≥2 例的≥3 级不良事件为贫血和高血压(n=2)。1 例患者达到确认的完全缓解(A 组),5 例患者达到确认的部分缓解(n=3,A 组;n=2,B 组)。客观缓解率和疾病控制率分别为 35.3%和 76.5%。在局部晚期/转移性尿路上皮癌的日本患者中,enfortumab vedotin 具有良好的耐受性,具有初步抗肿瘤活性,药代动力学特征与既往报道一致。