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用于可视化表达上皮细胞黏附分子(EpCAM)的肺癌的设计锚蛋白重复蛋白[锝]Tc(CO)-(HE)-Ec1的I期临床评估

Phase I Clinical Evaluation of Designed Ankyrin Repeat Protein [Tc]Tc(CO)-(HE)-Ec1 for Visualization of EpCAM-Expressing Lung Cancer.

作者信息

Zelchan Roman, Chernov Vladimir, Medvedeva Anna, Rybina Anastasia, Bragina Olga, Mishina Elizaveta, Larkina Mariia, Varvashenya Ruslan, Fominykh Anastasia, Schulga Alexey, Konovalova Elena, Vorobyeva Anzhelika, Orlova Anna, Tashireva Liubov, Deyev Sergey M, Tolmachev Vladimir

机构信息

Department of Nuclear Medicine, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, 634055 Tomsk, Russia.

Research Centrum for Oncotheranostics, Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, 634050 Tomsk, Russia.

出版信息

Cancers (Basel). 2024 Aug 10;16(16):2815. doi: 10.3390/cancers16162815.

Abstract

A high level of EpCAM overexpression in lung cancer makes this protein a promising target for targeted therapy. Radionuclide visualization of EpCAM expression would facilitate the selection of patients potentially benefiting from such treatment. Single-photon computed tomography (SPECT) using Tc-labeled engineered scaffold protein DARPin Ec1 has shown its effectiveness in imaging tumors with overexpression of EpCAM in preclinical studies, providing high contrast just a few hours after injection. This first-in-human study aimed to evaluate the safety and distribution of [Tc]Tc(CO)-(HE)-Ec1 in patients with primary lung cancer. Twelve lung cancer patients were injected with 300.7 ± 103.2 MBq of [Tc]Tc(CO)-(HE)-Ec1. Whole-body planar imaging (at 2, 4, 6 and 24 h after injection) and SPECT/CT of the lung (at 2, 4, and 6 h) were performed. The patients' vital signs and possible side effects were monitored up to 7 days after injection. The patients tolerated the injection of [Tc]Tc(CO)-(HE)-Ec1 well, and their somatic condition remained normal during the entire follow-up period. There were no abnormalities in blood and urine tests after injection of [Tc]Tc(CO)-(HE)-Ec1. The highest absorbed doses were in the kidneys, liver, pancreas, thyroid, gallbladder wall, and adrenals. There was also a relatively high accumulation of [Tc]Tc(CO)-(HE)-Ec1 in the small and large intestines, pancreas and thyroid. According to the SPECT/CT, accumulation of [Tc]Tc(CO)-(HE)-Ec1 in the lung tumor was found in all patients included in the study. Intensive accumulation of [Tc]Tc(CO)-(HE)-Ec1 was also noted in regional metastases. [Tc]Tc(CO)-(HE)-Ec1 can potentially be considered a diagnostic tracer for imaging EpCAM expression in lung cancer patients and other tumors with overexpression of EpCAM.

摘要

肺癌中高水平的上皮细胞黏附分子(EpCAM)过表达使得该蛋白成为靶向治疗的一个有前景的靶点。EpCAM表达的放射性核素显像将有助于选择可能从这种治疗中获益的患者。在临床前研究中,使用锝(Tc)标记的工程支架蛋白DARPin Ec1的单光子计算机断层扫描(SPECT)已显示出其在成像EpCAM过表达肿瘤方面的有效性,在注射后仅几小时就能提供高对比度。这项首次人体研究旨在评估[Tc]Tc(CO)-(HE)-Ec1在原发性肺癌患者中的安全性和分布情况。12例肺癌患者注射了300.7±103.2兆贝可的[Tc]Tc(CO)-(HE)-Ec1。进行了全身平面显像(注射后2、4、6和24小时)以及肺部的SPECT/CT(注射后2、4和6小时)。在注射后长达7天的时间里监测患者的生命体征和可能的副作用。患者对[Tc]Tc(CO)-(HE)-Ec1的注射耐受性良好,并且在整个随访期间其身体状况保持正常。注射[Tc]Tc(CO)-(HE)-Ec1后血液和尿液检查未发现异常。最高吸收剂量出现在肾脏、肝脏、胰腺、甲状腺、胆囊壁和肾上腺。[Tc]Tc(CO)-(HE)-Ec1在小肠、大肠、胰腺和甲状腺中也有相对较高的蓄积。根据SPECT/CT,在该研究纳入的所有患者中均发现[Tc]Tc(CO)-(HE)-Ec1在肺肿瘤中蓄积。在区域转移灶中也观察到[Tc]Tc(CO)-(HE)-Ec1的强烈蓄积。[Tc]Tc(CO)-(HE)-Ec1有可能被视为一种诊断性示踪剂,用于成像肺癌患者以及其他EpCAM过表达肿瘤中的EpCAM表达情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0f3/11353007/2b774f37942e/cancers-16-02815-g001.jpg

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