Fluorescent Diagnosis of Bladder Cancer by Hexasens as a Drug

Slovokhodov Egor Konstantinovich, Ivanova-Radkevich Veronika Igorevna, Brodsky Ilya Borisovich
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引用次数: 2

Abstract

This study was performed as a clinical trial conducted in Russia concerning the diagnostic efficacy of Hexasens drug. The photosensitizer based on hexyl ester of 5-aminolevulinic acid was used for the fluorescence diagnosis of bladder cancer. The study was conducted in 2015-2016 on the basis of the City Clinical Hospital No. 40 (Moscow, Russia). 53 patients were involved into study and were diagnosed as bladder cancer in T1N0M0 stage. Fluorescence diagnosis was carried out for 1 hour after the intravesical induction of 0.2% solution (50 mL or 100 mg) of Hexasens drug (FSUE "SSC NIOPIK", Russia). The results of the fluorescence diagnosis were compared with the results of the standard routine cystoscopy. The found results showed that the performance of fluorescent diagnostics (FD) led to improve diagnostic sensitivity as 13.2% compared to standard cystoscopy (from 86.8% to 100%); the diagnosis accuracy increased as 8.8% (from 91.2% to 100%) and a negative predictive value increased as 20.9% (from 79.1% to 100%). During the carrying out of fluorescence diagnosis, 8 patients (15.0%) out of 53 ones also revealed 14 fluorescing foci that not identified in white light, in which the tumorous process in them was confirmed during morphological study. The induction of Hexasens solution into a bladder and the carrying out of a fluorescent diagnosis was not accompanied by the development of any adverse reactions. Patients showed a subjective discomfort only during a prolonged exposure of the drug solution in a bladder (up to 2 hours). The developed diagnosis methods is recommended for the applying in advanced clinical diagnosis.
Hexasens作为药物的荧光诊断膀胱癌
本研究是在俄罗斯进行的一项关于Hexasens药物诊断疗效的临床试验。以5-氨基乙酰丙酸己基酯为基础的光敏剂用于膀胱癌的荧光诊断。该研究于2015-2016年在莫斯科第40市临床医院(俄罗斯)进行。53例膀胱癌患者被诊断为T1N0M0期。用0.2% Hexasens药物溶液(50 mL或100 mg) (FSUE“SSC NIOPIK”,俄罗斯)膀胱诱导1小时后进行荧光诊断。荧光诊断结果与标准常规膀胱镜检查结果进行比较。结果表明,与标准膀胱镜检查相比,荧光诊断(FD)的诊断灵敏度提高了13.2%(从86.8%提高到100%);诊断正确率提高了8.8%(从91.2%提高到100%),阴性预测值提高了20.9%(从79.1%提高到100%)。在进行荧光诊断时,53例患者中有8例(15.0%)还发现了14个白光下未发现的荧光灶,形态学研究证实了其肿瘤进程。将Hexasens溶液导入膀胱并进行荧光诊断,未出现任何不良反应。患者仅在药物溶液长期暴露于膀胱(长达2小时)时才表现出主观不适。所建立的诊断方法可用于临床高级诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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