Department of Urology, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Intuitive Surgical, Sunnyvale, CA, USA.
Eur Urol Oncol. 2024 Feb;7(1):63-72. doi: 10.1016/j.euo.2023.07.004. Epub 2023 Jul 27.
Men with high-risk prostate cancer undergoing surgery likely recur due to failure to completely excise regional and/or local disease.
The first-in-human evaluation of safety, pharmacokinetics, and exploratory efficacy of IS-002, a novel near-infrared prostate-specific membrane antigen (PSMA)-targeted fluorescence imaging agent, designed for intraoperative prostate cancer visualization.
DESIGN, SETTING, AND PARTICIPANTS: A phase 1, single-center, dose-escalation study was conducted in 24 men with high-risk prostate cancer scheduled for robotic-assisted radical prostatectomy with (extended) pelvic lymph node dissection using the da Vinci surgical system.
Adverse events (AEs), vital signs, complete blood count, complete metabolic panel, urinalysis, and electrocardiogram were assessed over a 14-d period and compared with baseline. The pharmacokinetic profile of IS-002 was determined. Diagnostic accuracy was assessed for exploratory efficacy.
AEs predominantly included discoloration of urine (n = 22/24; expected, related, grade 1). There were no grade ≥2 AEs. IS-002 C and area under the curve increased with increasing dose. Plasma concentrations declined rapidly in a biphasic manner, with the median terminal half-lives ranging from 5.0 to 7.6 h, independent of dose and renal function. At 25 μg/kg, the exploratory efficacy readouts for the negative and positive predictive values were, 97% and 45% for lymph nodes, and 100% and 80% for residual/locoregional disease detection, respectively.
IS-002 is safe and well tolerated, and has the potential to enable intraoperative tumor detection that could not be identified using standard imaging.
IS-002 is a new imaging agent that specifically targets the prostate-specific membrane antigen receptor. In this study, we tested IS-002 for the first time in men with high-risk prostate cancer undergoing surgery and found that IS-002 is safe, is cleared from the body quickly, and potentially allows identification of prostate cancer in areas that would not be identified by conventional white light imaging.
接受手术的高危前列腺癌男性可能会因未能完全切除局部和/或区域疾病而复发。
首次评估新型近红外前列腺特异性膜抗原(PSMA)靶向荧光成像剂 IS-002 的安全性、药代动力学和探索性疗效,该药物旨在术中可视化前列腺癌。
设计、地点和参与者:在一项单中心、剂量递增的 24 名高危前列腺癌男性的 1 期临床试验中,使用达芬奇手术系统进行机器人辅助根治性前列腺切除术(扩大)盆腔淋巴结清扫术。
不良反应(AE)主要包括尿液变色(24/24;预期、相关、1 级)。无 2 级以上 AE。IS-002 的 C 和曲线下面积随剂量增加而增加。血浆浓度呈双相快速下降,中位终末半衰期范围为 5.0 至 7.6 小时,与剂量和肾功能无关。在 25μg/kg 时,用于检测淋巴结的阴性和阳性预测值的探索性疗效读数分别为 97%和 45%,用于检测残留/局部疾病的分别为 100%和 80%。
IS-002安全且耐受良好,具有潜在能力实现术中肿瘤检测,而这是标准成像无法识别的。
IS-002 是一种新型成像剂,专门针对前列腺特异性膜抗原受体。在这项研究中,我们首次在接受手术的高危前列腺癌男性中测试了 IS-002,发现 IS-002是安全的,能快速从体内清除,并有可能识别常规白光成像无法识别的前列腺癌区域。