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Supporting the stratification of non-small cell lung carcinoma for Anti PD-L1 immunotherapy with digital image registration

机译:通过数字图像配准支持非小细胞肺癌分层用于抗PD-L1免疫治疗

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The analysis of differently-stained pathology slides constitutes an important way of collecting both morphological and functional tissue-related information and is a widely used as a tool for stratification of the diagnosis of a wide range on oncological diseases. Due to deformations induced during the sectioning process and the need to view differently stained slides alternately, or using multiple microscopes, such combined analysis corresponds to an inefficient and prone to error process. In this work we propose a fast and semi-supervised algorithm which extends a multiresolution approach, adopted from methods in literature that firstly addressed the problem of combined analysis of tissue slides using intensity-based registration of whole-slide scanned images. Our method suggests that the inclusion of a supervised step substantially contributes to the complexity reduction of the registration problem, allowing to halve the number of resolutions used by the registration algorithm without compromising a rapid and accurate approximation of tissue slides alignment at a zoom level of 40x, thus representing a well-adapted solution for pathology labs.
机译:分析不同染色的病理切片是收集形态学和功能性组织相关信息的重要方式,并且被广泛用作对广泛的肿瘤疾病进行诊断的分层工具。由于在切片过程中引起的变形以及需要交替查看不同染色的载玻片或使用多个显微镜,这种组合分析对应于效率低下且易于出错的过程。在这项工作中,我们提出了一种快速和半监督的算法,该算法扩展了多分辨率方法,该方法从文献中的方法开始采用,该方法首先解决了使用基于强度的全玻片扫描图像配准对组织玻片进行组合分析的问题。我们的方法表明,包含监督步骤可极大地减少配准问题的复杂度,从而使配准算法使用的分辨率减少一半,而不会以40倍缩放级别影响组织切片的快速,准确近似。 ,因此代表了病理实验室的一种很好的解决方案。

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