Hyperspectral imaging of Kaposi's Sarcoma for disease assessment and treatment monitoring

D. Hattery, Moinuddin Hassan, S. Demos, A. Gandjbakhche
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引用次数: 15

Abstract

Light spectroscopic methods are critical to advances in molecular characterization of disease processes. However, these methods have been limited to in-vitro or cell culture studies. In fact, strong scattering in almost all tissue types causes dispersion of the photons paths which results in poor localization and resolution. Hence, quantitative analysis of spectral data obtained from structures below the tissue surface requires accounting for scattering which affects both the penetration of the photons and the path length over which the photons will be subject to molecularly specific absorption. The goal of much current research is to non-invasively obtain diagnostically useful molecular information from embedded sites. We have designed and built a six-band multi-spectral NIR imaging system which we have used on patients with highly vascularized tumors in the skin called Kaposi's Sarcoma. The imaged lesions are undergoing treatment with experimental anti-angiogenesis drugs that are designed to reduce bloodflow and hence growth of the tumors. The NIR data is combined with both 3-5 micron and 8-12 micron infrared images, obtained of the same tumors, which are used to identify thermal signatures of blood volume, as well as three-band visible wavelength data which show the visible extent of the lesions. We have developed a layered model of the skin in which specific analytes exist in specific layers. The spectral signatures of analytes such as oxy- and deoxy-hemoglobin are known. To obtain information on the concentration of those analytes in the tissue, however, the diffuse reflectance NIR images from the patients must be corrected for scattering. The scattering is modeled using analytical solutions developed from a random walk model of photon migration in turbid media. When the hyperspectral patient data is fit to the model, physiologically related parameters, such as to blood volume and oxygenation, are obtained. This provides clinically important data that may be used by the physician for evaluations of drug effectiveness, disease assessment and patient treatment monitoring.
卡波西肉瘤的高光谱成像用于疾病评估和治疗监测
光谱学方法对疾病过程分子表征的进展至关重要。然而,这些方法仅限于体外或细胞培养研究。事实上,几乎所有组织类型中的强散射都会导致光子路径的色散,从而导致较差的定位和分辨率。因此,从组织表面以下的结构中获得的光谱数据的定量分析需要考虑散射,它既影响光子的穿透,也影响光子被分子特异性吸收的路径长度。目前许多研究的目标是从嵌入的位点非侵入性地获得诊断有用的分子信息。我们设计并建造了一个六波段多光谱近红外成像系统,我们已经将其用于皮肤上高度血管化肿瘤的患者,称为卡波西肉瘤。成像的病变正在接受实验性抗血管生成药物的治疗,这种药物旨在减少血液流动,从而抑制肿瘤的生长。近红外数据与同一肿瘤获得的3-5微米和8-12微米红外图像相结合,用于识别血容量的热特征,以及显示病变可见范围的三波段可见波长数据。我们开发了一种皮肤的分层模型,其中特定的分析物存在于特定的层中。分析物如氧血红蛋白和脱氧血红蛋白的光谱特征是已知的。然而,为了获得组织中这些分析物浓度的信息,必须对患者的漫反射近红外图像进行散射校正。散射是用在浑浊介质中光子迁移的随机游走模型上的解析解来模拟的。当高光谱患者数据与模型拟合时,可以获得生理相关参数,如血容量和氧合。这提供了临床上重要的数据,可用于医生评估药物有效性,疾病评估和患者治疗监测。
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