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arXiv 2406.07061eess.IVcs.CV

通过2.5D多实例学习对3D病理数据进行分诊以指导病理学家评估

Triage of 3D pathology data via 2.5D multiple-instance learning to guide pathologist assessments

University of Washington(华盛顿大学);Mass General Brigham(麻省总医院布里格姆医疗系统);Harvard University(哈佛大学)

Gan Gao, Andrew H. Song, Fiona Wang, David Brenes, Rui Wang, Sarah S. L. Chow, Kevin W. Bishop, Lawrence D. True, Faisal Mahmood, Jonathan T. C. Liu

AI总结:

本文提出CARP3D深度学习方法,通过2.5D多实例学习自动识别3D活检中的高风险2D切片,在前列腺癌风险分层中AUC达90.4%,可辅助病理学家高效审查。

摘要:

当前临床实践中,病理学家仅评估从3D体积组织中切取的数量有限的薄2D组织切片,这阻碍了基于人体组织活检的准确患者诊断。非破坏性3D病理学的最新进展,如开放式顶板光片显微镜,能够对空间异质性组织形态进行全面成像,为提高诊断确定性提供了可行性。3D病理学临床采用的一条潜在早期途径是依靠病理学家基于查看3D数据集中熟悉的2D H&E样图像切片来做出最终诊断。然而,人工检查海量3D病理数据集是不可行的。为解决这一问题,我们提出了CARP3D,一种深度学习分诊方法,可自动识别3D体积活检中风险最高的2D切片,从而使病理学家能够进行时间高效的审查。对于活检中的给定切片,我们通过对每个切片内的2D图像块进行基于注意力的聚合来估计其风险,然后对相邻切片进行池化以计算上下文感知的2.5D风险评分。在前列腺癌风险分层中,CARP3D在切片分诊方面实现了90.4%的曲线下面积(AUC),优于依赖2D切片独立分析的方法(AUC=81.3%)。这些结果表明,整合额外的深度上下文增强了模型的判别能力。总之,CARP3D有潜力通过在大体积3D病理数据集中准确分诊高风险切片来改进病理学家的诊断。

英文摘要:

Accurate patient diagnoses based on human tissue biopsies are hindered by current clinical practice, where pathologists assess only a limited number of thin 2D tissue slices sectioned from 3D volumetric tissue. Recent advances in non-destructive 3D pathology, such as open-top light-sheet microscopy, enable comprehensive imaging of spatially heterogeneous tissue morphologies, offering the feasibility to improve diagnostic determinations. A potential early route towards clinical adoption for 3D pathology is to rely on pathologists for final diagnosis based on viewing familiar 2D H&E-like image sections from the 3D datasets. However, manual examination of the massive 3D pathology datasets is infeasible. To address this, we present CARP3D, a deep learning triage approach that automatically identifies the highest-risk 2D slices within 3D volumetric biopsy, enabling time-efficient review by pathologists. For a given slice in the biopsy, we estimate its risk by performing attention-based aggregation of 2D patches within each slice, followed by pooling of the neighboring slices to compute a context-aware 2.5D risk score. For prostate cancer risk stratification, CARP3D achieves an area under the curve (AUC) of 90.4% for triaging slices, outperforming methods relying on independent analysis of 2D sections (AUC=81.3%). These results suggest that integrating additional depth context enhances the model's discriminative capabilities. In conclusion, CARP3D has the potential to improve pathologist diagnosis via accurate triage of high-risk slices within large-volume 3D pathology datasets.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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