Department of Colorectal Surgery, Advent Health, 2415 N Orange Ave Ste 300, Orlando, FL, 32804, USA.
Astellas Pharma Global Development, Inc., Northbrook, IL, USA.
Surg Endosc. 2023 Sep;37(9):7336-7347. doi: 10.1007/s00464-023-10193-9. Epub 2023 Jul 20.
Intraoperative ureteral injury, a serious complication of abdominopelvic surgeries, can be avoided through ureter visualization. Near-infrared fluorescence imaging offers real-time anatomical visualization of ureters during surgery. Pudexacianinium (ASP5354) chloride is an indocyanine green derivative under investigation for intraoperative ureter visualization during colorectal or gynecologic surgery in adult and pediatric patients.
In this phase 2 study (NCT04238481), adults undergoing laparoscopic colorectal surgery were randomized to receive one intravenous dose of pudexacianinium 0.3 mg, 1.0 mg, or 3.0 mg. The primary endpoint was successful intraoperative ureter visualization, defined as observation of ureter fluorescence 30 min after pudexacianinium administration and at end of surgery. Safety and pharmacokinetics were also assessed.
Participants received pudexacianinium 0.3 mg (n = 3), 1.0 mg (n = 6), or 3.0 mg (n = 3). Most participants were female (n = 10; 83.3%); median age was 54 years (range 24-69) and median BMI was 29.3 kg/m (range 18.7-38.1). Successful intraoperative ureter visualization occurred in 2/3, 5/6, and 3/3 participants who received pudexacianinium 0.3 mg, 1.0 mg, or 3.0 mg, respectively. Median intensity values per surgeon assessment were 1 (mild) with the 0.3-mg dose, 2 (moderate) with the 1.0-mg dose, and 3 (strong) with the 3.0-mg dose. A correlation was observed between qualitative (surgeon's recognition/identification of the ureter during surgery) and quantitative (video recordings of the surgeries after study completion) assessment of fluorescence intensity. Two participants experienced serious adverse events, none of which were drug-related toxicities. One adverse event (grade 1 proteinuria) was related to pudexacianinium. Plasma pudexacianinium concentrations were dose-dependent and the mean (± SD) percent excreted into urine during surgery was 22.3% ± 8.0% (0.3-mg dose), 15.6% ± 10.0% (1.0-mg dose), and 39.5% ± 12.4% (3.0-mg dose).
In this study, 1.0 and 3.0 mg pudexacianinium provided ureteral visualization for the duration of minimally invasive, laparoscopic colorectal procedures and was safe and well tolerated.
术中输尿管损伤是腹部和盆腔手术的严重并发症,可以通过输尿管可视化来避免。近红外荧光成像是一种实时解剖可视化技术,可在手术过程中观察输尿管。Pudexacianinium(ASP5354)氯化物是一种正在研究的吲哚菁绿衍生物,用于在成人和儿科患者的结直肠或妇科手术中进行术中输尿管可视化。
在这项 2 期研究(NCT04238481)中,接受腹腔镜结直肠手术的成年人被随机分配接受静脉注射 pudexacianinium 0.3mg、1.0mg 或 3.0mg。主要终点是术中输尿管可视化成功,定义为 pudexacianinium 给药后 30 分钟和手术结束时观察到输尿管荧光。还评估了安全性和药代动力学。
参与者接受了 pudexacianinium 0.3mg(n=3)、1.0mg(n=6)或 3.0mg(n=3)。大多数参与者为女性(n=10;83.3%);中位年龄为 54 岁(范围 24-69),中位 BMI 为 29.3kg/m(范围 18.7-38.1)。接受 pudexacianinium 0.3mg、1.0mg 或 3.0mg 的参与者分别有 2/3、5/6 和 3/3 名成功实现了术中输尿管可视化。根据每位外科医生的评估,中位数强度值分别为 1(轻度)、2(中度)和 3(强),与定量(研究完成后手术视频记录)评估荧光强度存在相关性。两名参与者经历了严重的不良事件,没有一个与药物相关的毒性。一种不良事件(1 级蛋白尿)与 pudexacianinium 有关。血浆 pudexacianinium 浓度与剂量相关,手术期间尿液中排泄的平均(±SD)百分比分别为 22.3%±8.0%(0.3mg 剂量)、15.6%±10.0%(1.0mg 剂量)和 39.5%±12.4%(3.0mg 剂量)。
在这项研究中,1.0mg 和 3.0mg 的 pudexacianinium 为微创腹腔镜结直肠手术期间的输尿管可视化提供了保障,且安全且耐受良好。