Predicting Metastasis Risk in Pancreatic Neuroendocrine Tumors Using Deep Learning Image Analysis

被引:20
作者
Klimov, Sergey [1 ,2 ]
Xue, Yue [3 ]
Gertych, Arkadiusz [4 ,5 ,6 ]
Graham, Rondell P. [7 ]
Jiang, Yi [2 ]
Bhattarai, Shristi [1 ]
Pandol, Stephen J. [8 ]
Rakha, Emad A. [9 ]
Reid, Michelle D. [10 ]
Aneja, Ritu [1 ]
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30302 USA
[2] Georgia State Univ, Dept Math & Stat, Atlanta, GA 30303 USA
[3] Northwestern Univ, Dept Pathol, Chicago, IL 60611 USA
[4] Cedars Sinai Med Ctr, Dept Surg, Los Angeles, CA 90048 USA
[5] Cedars Sinai Med Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90048 USA
[6] Silesian Tech Univ, Fac Biomed Engn, Zabrze, Poland
[7] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[8] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
[9] Univ Nottingham, Dept Cellular Pathol, Nottingham, England
[10] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
来源
FRONTIERS IN ONCOLOGY | 2021年 / 10卷
关键词
metastasis risk assessment; deep learning; histological image analysis; pancreatic neuroendocrine tumors; computational pathology;
D O I
10.3389/fonc.2020.593211
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The prognosis of patients with pancreatic neuroendocrine tumors (PanNET), the second most common type of pancreatic cancer, varies significantly, and up to 15% of patients develop metastasis. Although certain morphological characteristics of PanNETs have been associated with patient outcome, there are no available morphology-based prognostic markers. Given that current clinical histopathology markers are unable to identify high-risk PanNET patients, the development of accurate prognostic biomarkers is needed. Here, we describe a novel machine learning, multiclassification pipeline to predict the risk of metastasis using morphological information from whole tissue slides. Methods Digital images from surgically resected tissues from 89 PanNET patients were used. Pathologist-annotated regions were extracted to train a convolutional neural network (CNN) to identify tiles consisting of PanNET, stroma, normal pancreas parenchyma, and fat. Computationally annotated cancer or stroma tiles and patient metastasis status were used to train CNN to calculate a region based metastatic risk score. Aggregation of the metastatic probability scores across the slide was performed to predict the risk of metastasis. Results The ability of CNN to discriminate different tissues was high (per-tile accuracy >95%; whole slide cancer regions Jaccard index = 79%). Cancer and stromal tiles with high evaluated probability provided F1 scores of 0.82 and 0.69, respectively, when we compared tissues from patients who developed metastasis and those who did not. The final model identified low-risk (n = 76) and high-risk (n = 13) patients, as well as predicted metastasis-free survival (hazard ratio: 4.71) after adjusting for common clinicopathological variables, especially in grade I/II patients. Conclusion Using slides from surgically resected PanNETs, our novel, multiclassification, deep learning pipeline was able to predict the risk of metastasis in PanNET patients. Our results suggest the presence of prognostic morphological patterns in PanNET tissues, and that these patterns may help guide clinical decision making.
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页数:10
相关论文
共 49 条
  • [11] Neuroendocrine Tumors of the Pancreas
    Ehehalt, Florian
    Saeger, Hans D.
    Schmidt, C. Max
    Gruetzmann, Robert
    [J]. ONCOLOGIST, 2009, 14 (05) : 456 - 467
  • [12] Prognostic Factors and Survival in 324 Patients with Pancreatic Endocrine Tumor Treated at a Single Institution
    Ekeblad, Sara
    Skogseid, Britt
    Dunder, Kristina
    Oberg, Kjell
    Eriksson, Barbro
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (23) : 7798 - 7803
  • [13] Fischer L, 2008, BRIT J SURG, V95, P627, DOI 10.1002/bjs.6051
  • [14] Novel recurrence risk stratification of resected pancreatic neuroendocrine tumor
    Gao, Heli
    Liu, Liang
    Wang, Wenquan
    Xu, Huaxiang
    Jin, Kaizhou
    Wu, Chuntao
    Qi, Zihao
    Zhang, Shirong
    Liu, Chen
    Xu, Jinzhi
    Ni, Quanxing
    Yu, Xianjun
    [J]. CANCER LETTERS, 2018, 412 : 188 - 193
  • [15] Convolutional neural networks can accurately distinguish four histologic growth patterns of lung adenocarcinoma in digital slides
    Gertych, Arkadiusz
    Swiderska-Chadaj, Zaneta
    Ma, Zhaoxuan
    Ing, Nathan
    Markiewicz, Tomasz
    Cierniak, Szczepan
    Salemi, Hootan
    Guzman, Samuel
    Walts, Ann E.
    Knudsen, Beatrice S.
    [J]. SCIENTIFIC REPORTS, 2019, 9 (1)
  • [16] Pancreatic Neuroendocrine Tumors
    Hill, Joshua S.
    McPhee, James T.
    McDade, Theodore P.
    Zhou, Zheng
    Sullivan, Mary E.
    Whalen, Giles F.
    Tseng, Jennifer F.
    [J]. CANCER, 2009, 115 (04) : 741 - 751
  • [17] Predicting Prognosis in Gastroentero-Pancreatic Neuroendocrine Tumors: An Overview and the Value of Ki-67 Immunostaining
    Jamali, Mina
    Chetty, Runjan
    [J]. ENDOCRINE PATHOLOGY, 2008, 19 (04) : 282 - 288
  • [18] Stain Normalization using Sparse AutoEncoders (StalloSA): Application to digital pathology
    Janowczyk, Andrew
    Basavanhally, Ajay
    Madabhushi, Anant
    [J]. COMPUTERIZED MEDICAL IMAGING AND GRAPHICS, 2017, 57 : 50 - 61
  • [19] Cadherin 17 is frequently expressed by 'sclerosing variant' pancreatic neuroendocrine tumour
    Johnson, Adam
    Wright, Jesse P.
    Zhao, Zhiguo
    Komaya, Tatsuki
    Parikh, Alexander
    Merchant, Nipun
    Shi, Chanjuan
    [J]. HISTOPATHOLOGY, 2015, 66 (02) : 225 - 233
  • [20] Pan-cancer image-based detection of clinically actionable genetic alterations
    Kather, Jakob Nikolas
    Heij, Lara R.
    Grabsch, Heike I.
    Loeffler, Chiara
    Echle, Amelie
    Muti, Hannah Sophie
    Krause, Jeremias
    Niehues, Jan M.
    Sommer, Kai A. J.
    Bankhead, Peter
    Kooreman, Loes F. S.
    Schulte, Jefree J.
    Cipriani, Nicole A.
    Buelow, Roman D.
    Boor, Peter
    Ortiz-Bruechle, Nadina
    Hanby, Andrew M.
    Speirs, Valerie
    Kochanny, Sara
    Patnaik, Akash
    Srisuwananukorn, Andrew
    Brenner, Hermann
    Hoffmeister, Michael
    van den Brandt, Piet A.
    Jaeger, Dirk
    Trautwein, Christian
    Pearson, Alexander T.
    Luedde, Tom
    [J]. NATURE CANCER, 2020, 1 (08) : 789 - +