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Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples

Human tissue consists of complex structures that display a diversity of morphologies, forming a tissue microenvironment that is, by nature, three-dimensional (3D). However, the current standard-of-care involves slicing 3D tissue specimens into two-dimensional (2D) sections and selecting a few for mi...

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Autores principales: Song, Andrew H., Williams, Mane, Williamson, Drew F. K., Jaume, Guillaume, Zhang, Andrew, Chen, Bowen, Serafin, Robert, Liu, Jonathan T. C., Baras, Alex, Parwani, Anil V., Mahmood, Faisal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornell University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402184/
https://www.ncbi.nlm.nih.gov/pubmed/37547660
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author Song, Andrew H.
Williams, Mane
Williamson, Drew F. K.
Jaume, Guillaume
Zhang, Andrew
Chen, Bowen
Serafin, Robert
Liu, Jonathan T. C.
Baras, Alex
Parwani, Anil V.
Mahmood, Faisal
author_facet Song, Andrew H.
Williams, Mane
Williamson, Drew F. K.
Jaume, Guillaume
Zhang, Andrew
Chen, Bowen
Serafin, Robert
Liu, Jonathan T. C.
Baras, Alex
Parwani, Anil V.
Mahmood, Faisal
author_sort Song, Andrew H.
collection PubMed
description Human tissue consists of complex structures that display a diversity of morphologies, forming a tissue microenvironment that is, by nature, three-dimensional (3D). However, the current standard-of-care involves slicing 3D tissue specimens into two-dimensional (2D) sections and selecting a few for microscopic evaluation(1,2), with concomitant risks of sampling bias and misdiagnosis(3–6). To this end, there have been intense efforts to capture 3D tissue morphology and transition to 3D pathology, with the development of multiple high-resolution 3D imaging modalities(7–18). However, these tools have had little translation to clinical practice as manual evaluation of such large data by pathologists is impractical and there is a lack of computational platforms that can efficiently process the 3D images and provide patient-level clinical insights. Here we present Modality-Agnostic Multiple instance learning for volumetric Block Analysis (MAMBA), a deep-learning-based platform for processing 3D tissue images from diverse imaging modalities and predicting patient outcomes. Archived prostate cancer specimens were imaged with open-top light-sheet microscopy(12–14) or microcomputed tomography(15,16) and the resulting 3D datasets were used to train risk-stratification networks based on 5-year biochemical recurrence outcomes via MAMBA. With the 3D block-based approach, MAMBA achieves an area under the receiver operating characteristic curve (AUC) of 0.86 and 0.74, superior to 2D traditional single-slice-based prognostication (AUC of 0.79 and 0.57), suggesting superior prognostication with 3D morphological features. Further analyses reveal that the incorporation of greater tissue volume improves prognostic performance and mitigates risk prediction variability from sampling bias, suggesting that there is value in capturing larger extents of spatially heterogeneous 3D morphology. With the rapid growth and adoption of 3D spatial biology and pathology techniques by researchers and clinicians, MAMBA provides a general and efficient framework for 3D weakly supervised learning for clinical decision support and can help to reveal novel 3D morphological biomarkers for prognosis and therapeutic response.
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spelling pubmed-104021842023-08-05 Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples Song, Andrew H. Williams, Mane Williamson, Drew F. K. Jaume, Guillaume Zhang, Andrew Chen, Bowen Serafin, Robert Liu, Jonathan T. C. Baras, Alex Parwani, Anil V. Mahmood, Faisal ArXiv Article Human tissue consists of complex structures that display a diversity of morphologies, forming a tissue microenvironment that is, by nature, three-dimensional (3D). However, the current standard-of-care involves slicing 3D tissue specimens into two-dimensional (2D) sections and selecting a few for microscopic evaluation(1,2), with concomitant risks of sampling bias and misdiagnosis(3–6). To this end, there have been intense efforts to capture 3D tissue morphology and transition to 3D pathology, with the development of multiple high-resolution 3D imaging modalities(7–18). However, these tools have had little translation to clinical practice as manual evaluation of such large data by pathologists is impractical and there is a lack of computational platforms that can efficiently process the 3D images and provide patient-level clinical insights. Here we present Modality-Agnostic Multiple instance learning for volumetric Block Analysis (MAMBA), a deep-learning-based platform for processing 3D tissue images from diverse imaging modalities and predicting patient outcomes. Archived prostate cancer specimens were imaged with open-top light-sheet microscopy(12–14) or microcomputed tomography(15,16) and the resulting 3D datasets were used to train risk-stratification networks based on 5-year biochemical recurrence outcomes via MAMBA. With the 3D block-based approach, MAMBA achieves an area under the receiver operating characteristic curve (AUC) of 0.86 and 0.74, superior to 2D traditional single-slice-based prognostication (AUC of 0.79 and 0.57), suggesting superior prognostication with 3D morphological features. Further analyses reveal that the incorporation of greater tissue volume improves prognostic performance and mitigates risk prediction variability from sampling bias, suggesting that there is value in capturing larger extents of spatially heterogeneous 3D morphology. With the rapid growth and adoption of 3D spatial biology and pathology techniques by researchers and clinicians, MAMBA provides a general and efficient framework for 3D weakly supervised learning for clinical decision support and can help to reveal novel 3D morphological biomarkers for prognosis and therapeutic response. Cornell University 2023-07-27 /pmc/articles/PMC10402184/ /pubmed/37547660 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Song, Andrew H.
Williams, Mane
Williamson, Drew F. K.
Jaume, Guillaume
Zhang, Andrew
Chen, Bowen
Serafin, Robert
Liu, Jonathan T. C.
Baras, Alex
Parwani, Anil V.
Mahmood, Faisal
Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title_full Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title_fullStr Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title_full_unstemmed Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title_short Weakly Supervised AI for Efficient Analysis of 3D Pathology Samples
title_sort weakly supervised ai for efficient analysis of 3d pathology samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402184/
https://www.ncbi.nlm.nih.gov/pubmed/37547660
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