From the *Department of Urology, Academic Medical Center, Amsterdam, the Netherlands; †Bracco Suisse SA, Geneva Research Centre and Manufacturing Site, Plan-les-Ouates, Switzerland; ‡Advice-US Consulting, Nernier, France; and §Department of Pathology, Academic Medical Center, Amsterdam, the Netherlands.
Invest Radiol. 2017 Jul;52(7):419-427. doi: 10.1097/RLI.0000000000000362.
BR55, a vascular endothelial growth factor receptor 2 (VEGFR2)-specific ultrasound molecular contrast agent (MCA), has shown promising results in multiple preclinical models regarding cancer imaging. In this first-in-human, phase 0, exploratory study, we investigated the feasibility and safety of the MCA for the detection of prostate cancer (PCa) in men using clinical standard technology.
Imaging with the MCA was performed in 24 patients with biopsy-proven PCa scheduled for radical prostatectomy using a clinical ultrasound scanner at low acoustic power. Safety monitoring was done by physical examination, blood pressure and heart rate measurements, electrocardiogram, and blood sampling. As first-in-human study, MCA dosing and imaging protocol were necessarily fine-tuned along the enrollment to improve visualization. Imaging data were correlated with radical prostatectomy histopathology to analyze the detection rate of ultrasound molecular imaging with the MCA.
Imaging with MCA doses of 0.03 and 0.05 mL/kg was adequate to obtain contrast enhancement images up to 30 minutes after administration. No serious adverse events or clinically meaningful changes in safety monitoring data were identified during or after administration. BR55 dosing and imaging were fine-tuned in the first 12 patients leading to 12 subsequent patients with an improved MCA dosing and imaging protocol. Twenty-three patients underwent radical prostatectomy. A total of 52 lesions were determined to be malignant by histopathology with 26 (50%) of them seen during BR55 imaging. In the 11 patients that were scanned with the improved protocol and underwent radical prostatectomy, a total of 28 malignant lesions were determined: 19 (68%) were seen during BR55 ultrasound molecular imaging, whereas 9 (32%) were not identified.
Ultrasound molecular imaging with BR55 is feasible with clinical standard technology and demonstrated a good safety profile. Detectable levels of the MCA can be reached in patients with PCa opening the way for further clinical trials.
BR55 是一种血管内皮生长因子受体 2(VEGFR2)特异性超声分子对比剂(MCA),在多种临床前模型中对癌症成像的研究显示出了良好的效果。在这项首次人体、探索性、0 期临床试验中,我们使用临床标准技术研究了 MCA 用于检测前列腺癌(PCa)的可行性和安全性。
在 24 名经活检证实患有 PCa 并计划接受根治性前列腺切除术的患者中,使用临床超声扫描仪在低声功率下进行 MCA 成像。通过体格检查、血压和心率测量、心电图和血液采样进行安全性监测。由于这是一项首次人体研究,MCA 的给药剂量和成像方案在招募过程中进行了必要的调整,以提高可视化效果。将成像数据与根治性前列腺切除术的组织病理学相关联,以分析 MCA 超声分子成像的检测率。
MCA 剂量为 0.03 和 0.05 mL/kg 时,可以获得足够的对比增强图像,在给药后 30 分钟内均可进行。在给药期间或之后,未发现严重不良事件或安全性监测数据的有临床意义的变化。在最初的 12 名患者中对 BR55 给药剂量和成像方案进行了调整,随后对 12 名后续患者进行了调整,改进了 MCA 的给药剂量和成像方案。23 名患者接受了根治性前列腺切除术。组织病理学共确定 52 个病灶为恶性,其中 26 个(50%)在 BR55 成像时可见。在接受改良方案扫描并接受根治性前列腺切除术的 11 名患者中,共确定 28 个恶性病灶:19 个(68%)在 BR55 超声分子成像时可见,而 9 个(32%)未识别。
使用临床标准技术进行 BR55 的超声分子成像具有可行性,并显示出良好的安全性。可以在患有 PCa 的患者中达到 MCA 的可检测水平,为进一步的临床试验开辟了道路。