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Fluorescence spectroscopy incorporating a ratiometric approach for the diagnosis and classification of urothelial carcinoma

机译:荧光光谱掺入尿路上皮癌的诊断和分类的比例方法

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The current most popular clinical method for the screening of urothelial carcinoma is white light cystoscopy. This method has inherent disadvantages making a strong genesis towards developing more powerful diagnostic techniques. Laser induced intrinsic fluorescence spectroscopy has been studied as an adjunct to current methods for the detection of tumors. This technique allows real time results based on the changes in spectral profile between normal and tumor tissues. We conducted a pilot study based on fluorescence spectroscopy at two wavelengths 378 and 445 nm excitation for the differentiation of urothelial carcinoma. At both the excitation wavelengths, the measured fluorescence signal showed an increased intensity at wavelengths greater than 520 nm. In addition, the emission profile showed modulation at 580 nm which is due to the reabsorption of emitted fluorescence due to hemoglobin. Additionally, we developed a tissue characterizing algorithm, based on fluorescence intensity ratios, F510/F600 and F520/F580 at 378 and 445 nm excitation wavelengths respectively. Further, the results were correlated with the pathologists assessment of urothelial carcinoma. This ratiometric classification algorithm yielded 81% sensitivity and 83% specificity at 378 nm and while at 445 nm excitation we achieved a sensitivity and specificity of 85% and 86% for classifying normal and tumor bladder tissues. In this study we have demonstrated the potential of a simple ratiometric algorithm based on fluorescence spectroscopy could be an alternative tool to tissue biopsy. Furthermore, this technique based fiber-based fluorescence spectroscopy could be integrated into an endoscopy system for use in the operating room.
机译:目前最受欢迎的筛查尿路上皮癌的临床方法是白光膀胱镜检查。这种方法具有固有的缺点,使得强烈的成因促进更强大的诊断技术。激光诱导的内在荧光光谱研究已被研究作为检测肿瘤的当前方法的辅助方法。该技术允许基于正常和肿瘤组织之间的光谱分布的变化来实时结果。我们在两个波长378和445nm激发中基于荧光光谱进行了试验研究,用于分化尿路上皮癌。在激发波长的两个中,测量的荧光信号显示出大于520nm的波长的增加的强度。此外,发射曲线显示为580nm的调节,这是由于血红蛋白引起的发射荧光的重吸收。另外,我们分别在378和445nm激发波长下基于荧光强度比,F510 / F600和F520 / F580进行组织表征算法。此外,结果与尿路上皮癌的病理学家评估相关。该比例分类算法在378nm处产生81%的灵敏度和83%的特异性,而在445nm激发下,我们达到了对正常和肿瘤膀胱组织进行了85%和86%的敏感性和特异性。在该研究中,我们已经证明了一种基于荧光光谱的简单比例算法的潜力可以是组织活检的替代工具。此外,该技术基于纤维基荧光光谱可以集成到内窥镜系统中以用于手术室。

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