Department of Surgery, Radboud University Nijmegen Medical Center, Nijmegen, the Netherlands.
Cancer. 2010 Feb 15;116(4 Suppl):1111-7. doi: 10.1002/cncr.24799.
Antibody-based imaging agents are available commercially, but their success has been limited, mainly because of low contrast and the emergence of 2-fluoro-2-deoxy-D-glucose-positron emission tomography (FDG-PET) scanning. In pretargeting, administration of the radionuclide is separated from the antibody, thereby enhancing image contrast and allowing detection at earlier time points after injection.
The authors conducted an open-label, single-arm trial that assessed a pretargeting procedure in which an anticarcinoembryonic antigen x (anti-CEA x) anti-diethylenetriaminepentaacetic acid (anti-DTPA)-indum (In) antibody was used in combination with a (111)In-labeled di-DTPA peptide for the diagnostic imaging of CEA-expressing colorectal cancer. Three patients received the (111)In peptide alone to investigate tumor targeting, organ distribution, and clearance of the peptide. Thereafter, 11 patients received the bispecific antibody (bsAb) (5 mg) to pretarget the tumor. After 3 to 5 days, patients were injected with 185 megabecquerels of (111)In-labeled peptide to assess the optimal interval for best image quality.
Fourteen patients with primary colorectal cancer were enrolled. One of 3 patients who received (111)In peptide alone had low-level tumor uptake. In 9 of 11 other patients, tumors were observed. In 1 patient, FDG-PET-positive lymph nodes were observed clearly with pretargeted immunoscintigraphy. Peptide pharmacokinetics revealed enhanced circulating levels of (111)In-labeled peptide in patients in the 3-day interval cohort compared with the other cohorts. Tumor-to-background ratios ranged from 3.5 to 6.4 in the 3-day interval group, from 5.1 to 14.2 in the 4-day interval group, and from 3.5 to 3.9 in the 5-day interval group. The best images were acquired with a 4-day interval at 24 hours after injection of the radiolabeled peptide. Grade 1 adverse events were observed in 2 patients.
Imaging of colorectal cancer using a 2-step, pretargeting system produced the best imaging results 24 hours after peptide administration using a 4-day interval between injection of the bsAb and the peptide.
已有商业化的抗体类成像剂,但由于对比度低以及 2-氟-2-脱氧-D-葡萄糖正电子发射断层扫描(FDG-PET)的出现,其应用受到限制。在预靶向中,放射性核素的给药与抗体分离,从而提高了图像对比度,并允许在注射后更早的时间点进行检测。
作者进行了一项开放标签、单臂试验,评估了一种预靶向程序,该程序中使用抗癌胚抗原 x(抗-CEA x)抗二乙三胺五乙酸(抗-DTPA)-铟(In)抗体与(111)In 标记的二-DTPA 肽联合用于诊断表达癌胚抗原的结直肠癌。3 名患者单独接受(111)In 肽以研究肿瘤靶向、器官分布和肽的清除。此后,11 名患者接受双特异性抗体(bsAb)(5mg)进行肿瘤预靶向。3 至 5 天后,患者接受 185MBq 的(111)In 标记肽以评估获得最佳图像质量的最佳时间间隔。
共纳入 14 名原发性结直肠癌患者。单独接受(111)In 肽的 3 名患者中有 1 名肿瘤摄取水平低。在其他 11 名患者中的 9 名中观察到肿瘤。在 1 名患者中,用预靶向免疫闪烁成像清楚地观察到 FDG-PET 阳性的淋巴结。肽药代动力学显示,与其他队列相比,在 3 天间隔组的患者中,(111)In 标记肽的循环水平更高。在 3 天间隔组中,肿瘤与背景的比值范围为 3.5 至 6.4,在 4 天间隔组中为 5.1 至 14.2,在 5 天间隔组中为 3.5 至 3.9。在注射放射性标记肽后 24 小时,最佳图像在 4 天间隔获得。2 名患者发生 1 级不良事件。
使用两步预靶向系统对结直肠癌进行成像,在注射 bsAb 和肽之间间隔 4 天,在注射后 24 小时使用肽,可获得最佳的成像结果。