Cargando…

Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis

Prostate cancer treatment planning is largely dependent upon examination of core-needle biopsies. The microscopic architecture of the prostate glands forms the basis for prognostic grading by pathologists. Interpretation of these convoluted three-dimensional (3D) glandular structures via visual insp...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Weisi, Reder, Nicholas P., Koyuncu, Can, Leo, Patrick, Hawley, Sarah, Huang, Hongyi, Mao, Chenyi, Postupna, Nadia, Kang, Soyoung, Serafin, Robert, Gao, Gan, Han, Qinghua, Bishop, Kevin W., Barner, Lindsey A., Fu, Pingfu, Wright, Jonathan L., Keene, C. Dirk, Vaughan, Joshua C., Janowczyk, Andrew, Glaser, Adam K., Madabhushi, Anant, True, Lawrence D., Liu, Jonathan T.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803395/
https://www.ncbi.nlm.nih.gov/pubmed/34853071
http://dx.doi.org/10.1158/0008-5472.CAN-21-2843
_version_ 1784642859935203328
author Xie, Weisi
Reder, Nicholas P.
Koyuncu, Can
Leo, Patrick
Hawley, Sarah
Huang, Hongyi
Mao, Chenyi
Postupna, Nadia
Kang, Soyoung
Serafin, Robert
Gao, Gan
Han, Qinghua
Bishop, Kevin W.
Barner, Lindsey A.
Fu, Pingfu
Wright, Jonathan L.
Keene, C. Dirk
Vaughan, Joshua C.
Janowczyk, Andrew
Glaser, Adam K.
Madabhushi, Anant
True, Lawrence D.
Liu, Jonathan T.C.
author_facet Xie, Weisi
Reder, Nicholas P.
Koyuncu, Can
Leo, Patrick
Hawley, Sarah
Huang, Hongyi
Mao, Chenyi
Postupna, Nadia
Kang, Soyoung
Serafin, Robert
Gao, Gan
Han, Qinghua
Bishop, Kevin W.
Barner, Lindsey A.
Fu, Pingfu
Wright, Jonathan L.
Keene, C. Dirk
Vaughan, Joshua C.
Janowczyk, Andrew
Glaser, Adam K.
Madabhushi, Anant
True, Lawrence D.
Liu, Jonathan T.C.
author_sort Xie, Weisi
collection PubMed
description Prostate cancer treatment planning is largely dependent upon examination of core-needle biopsies. The microscopic architecture of the prostate glands forms the basis for prognostic grading by pathologists. Interpretation of these convoluted three-dimensional (3D) glandular structures via visual inspection of a limited number of two-dimensional (2D) histology sections is often unreliable, which contributes to the under- and overtreatment of patients. To improve risk assessment and treatment decisions, we have developed a workflow for nondestructive 3D pathology and computational analysis of whole prostate biopsies labeled with a rapid and inexpensive fluorescent analogue of standard hematoxylin and eosin (H&E) staining. This analysis is based on interpretable glandular features and is facilitated by the development of image translation–assisted segmentation in 3D (ITAS3D). ITAS3D is a generalizable deep learning–based strategy that enables tissue microstructures to be volumetrically segmented in an annotation-free and objective (biomarker-based) manner without requiring immunolabeling. As a preliminary demonstration of the translational value of a computational 3D versus a computational 2D pathology approach, we imaged 300 ex vivo biopsies extracted from 50 archived radical prostatectomy specimens, of which, 118 biopsies contained cancer. The 3D glandular features in cancer biopsies were superior to corresponding 2D features for risk stratification of patients with low- to intermediate-risk prostate cancer based on their clinical biochemical recurrence outcomes. The results of this study support the use of computational 3D pathology for guiding the clinical management of prostate cancer. SIGNIFICANCE: An end-to-end pipeline for deep learning–assisted computational 3D histology analysis of whole prostate biopsies shows that nondestructive 3D pathology has the potential to enable superior prognostic stratification of patients with prostate cancer.
format Online
Article
Text
id pubmed-8803395
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Association for Cancer Research
record_format MEDLINE/PubMed
spelling pubmed-88033952022-01-31 Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis Xie, Weisi Reder, Nicholas P. Koyuncu, Can Leo, Patrick Hawley, Sarah Huang, Hongyi Mao, Chenyi Postupna, Nadia Kang, Soyoung Serafin, Robert Gao, Gan Han, Qinghua Bishop, Kevin W. Barner, Lindsey A. Fu, Pingfu Wright, Jonathan L. Keene, C. Dirk Vaughan, Joshua C. Janowczyk, Andrew Glaser, Adam K. Madabhushi, Anant True, Lawrence D. Liu, Jonathan T.C. Cancer Res Convergence and Technologies Prostate cancer treatment planning is largely dependent upon examination of core-needle biopsies. The microscopic architecture of the prostate glands forms the basis for prognostic grading by pathologists. Interpretation of these convoluted three-dimensional (3D) glandular structures via visual inspection of a limited number of two-dimensional (2D) histology sections is often unreliable, which contributes to the under- and overtreatment of patients. To improve risk assessment and treatment decisions, we have developed a workflow for nondestructive 3D pathology and computational analysis of whole prostate biopsies labeled with a rapid and inexpensive fluorescent analogue of standard hematoxylin and eosin (H&E) staining. This analysis is based on interpretable glandular features and is facilitated by the development of image translation–assisted segmentation in 3D (ITAS3D). ITAS3D is a generalizable deep learning–based strategy that enables tissue microstructures to be volumetrically segmented in an annotation-free and objective (biomarker-based) manner without requiring immunolabeling. As a preliminary demonstration of the translational value of a computational 3D versus a computational 2D pathology approach, we imaged 300 ex vivo biopsies extracted from 50 archived radical prostatectomy specimens, of which, 118 biopsies contained cancer. The 3D glandular features in cancer biopsies were superior to corresponding 2D features for risk stratification of patients with low- to intermediate-risk prostate cancer based on their clinical biochemical recurrence outcomes. The results of this study support the use of computational 3D pathology for guiding the clinical management of prostate cancer. SIGNIFICANCE: An end-to-end pipeline for deep learning–assisted computational 3D histology analysis of whole prostate biopsies shows that nondestructive 3D pathology has the potential to enable superior prognostic stratification of patients with prostate cancer. American Association for Cancer Research 2022-01-15 2021-12-01 /pmc/articles/PMC8803395/ /pubmed/34853071 http://dx.doi.org/10.1158/0008-5472.CAN-21-2843 Text en ©2021 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Convergence and Technologies
Xie, Weisi
Reder, Nicholas P.
Koyuncu, Can
Leo, Patrick
Hawley, Sarah
Huang, Hongyi
Mao, Chenyi
Postupna, Nadia
Kang, Soyoung
Serafin, Robert
Gao, Gan
Han, Qinghua
Bishop, Kevin W.
Barner, Lindsey A.
Fu, Pingfu
Wright, Jonathan L.
Keene, C. Dirk
Vaughan, Joshua C.
Janowczyk, Andrew
Glaser, Adam K.
Madabhushi, Anant
True, Lawrence D.
Liu, Jonathan T.C.
Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title_full Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title_fullStr Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title_full_unstemmed Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title_short Prostate Cancer Risk Stratification via Nondestructive 3D Pathology with Deep Learning–Assisted Gland Analysis
title_sort prostate cancer risk stratification via nondestructive 3d pathology with deep learning–assisted gland analysis
topic Convergence and Technologies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8803395/
https://www.ncbi.nlm.nih.gov/pubmed/34853071
http://dx.doi.org/10.1158/0008-5472.CAN-21-2843
work_keys_str_mv AT xieweisi prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT redernicholasp prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT koyuncucan prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT leopatrick prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT hawleysarah prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT huanghongyi prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT maochenyi prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT postupnanadia prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT kangsoyoung prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT serafinrobert prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT gaogan prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT hanqinghua prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT bishopkevinw prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT barnerlindseya prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT fupingfu prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT wrightjonathanl prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT keenecdirk prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT vaughanjoshuac prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT janowczykandrew prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT glaseradamk prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT madabhushianant prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT truelawrenced prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis
AT liujonathantc prostatecancerriskstratificationvianondestructive3dpathologywithdeeplearningassistedglandanalysis