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Reproducibility of an Imaging Based Prostate Cancer Prognostic Assay

机译:基于影像学的前列腺癌预后分析的可重复性

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The Prostate Px⊕ prognostic assay offered by Aureon Biosciences is designed to predict progression post primary treatment for prostate cancer patients based on their diagnostic biopsy specimen. The assay is driven by the automated image analysis of biological specimens. Three different histological sections are analyzed for morphometric as well as immunofluorescence protein expression properties within areas of tumor digitally masked by expert pathologists. The assay was developed on a multi-institution cohort of up to 9 images from each of 1027 patients. The variation in histological sections, staining, pathologist tumor masking and the region of image acquisition all have the potential to significantly impact imaging features and consequently the reproducibility of the assay's results for the same patient. This study analyzed the reproducibility of the assay in 50 patients who were re-processed within 3 months in a blinded fashion as de-novo patients. The key assay results reported were in agreement in 94% of the cases. The two independent endpoints of risk classification reproduced results in 90% and 92% of the predictions. This work presents one of the first assessments of the reproducibility of a commercial assay's results given the inherent variations in images and quantitative imaging characteristics in a commercial setting.
机译:Aureon Biosciences提供的ProstatePx⊕预后测定旨在根据诊断性活检标本预测前列腺癌患者初次治疗后的进展。该测定是由生物样本的自动图像分析驱动的。分析了三个不同的组织学切片,以了解由专业病理学家数位掩盖的肿瘤区域内的形态学以及免疫荧光蛋白表达特性。该分析是在多机构队列中开发的,该队列最多包含1027位患者中每位患者的9张图像。组织切片的变化,染色,病理学家的肿瘤掩盖和图像采集区域都有可能显着影响成像特征,因此对同一患者的测定结果具有可重复性。这项研究分析了50例患者的检测方法的可重复性,这些患者在3个月内以盲法重新接受了de-novo患者的治疗。报告的关键检测结果在94%的病例中一致。风险分类的两个独立端点重现了90%和92%的预测结果。鉴于在商业环境中图像和定量成像特性的固有差异,这项工作提出了对商业化验结果可重复性的第一批评估之一。

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