Abstract
The convergence of digital pathology and computer vision is increasingly enabling computers to perform tasks performed by humans. As a result, artificial intelligence (AI) is having an astoundingly positive effect on the field of pathology, including breast pathology. Research using machine learning and the development of algorithms that learn patterns from labeled digital data based on “deep learning” neural networks and feature-engineered approaches to analyze histology images have recently provided promising results. Thus far, image analysis and more complex AI-based tools have demonstrated excellent success performing tasks such as the quantification of breast biomarkers and Ki67, mitosis detection, lymph node metastasis recognition, tissue segmentation for diagnosing breast carcinoma, prognostication, computational assessment of tumor-infiltrating lymphocytes, and prediction of molecular expression as well as treatment response and benefit of therapy from routine H&E images. This review critically examines the literature regarding these applications of AI in the area of breast pathology.
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References
Hamet P, Tremblay J (2017) Artificial intelligence in medicine. Metabolism 69:S36–S40. https://doi.org/10.1016/j.metabol.2017.01.011
Holzinger A (2019) Introduction to MAchine Learning & Knowledge Extraction (MAKE). Mach Learn Knowl Extr 1:1–20. https://doi.org/10.3390/make1010001
Basavanhally A, Feldman M, Shih N et al (2011) Multi-field-of-view strategy for image-based outcome prediction of multi-parametric estrogen receptor-positive breast cancer histopathology: comparison to Oncotype DX. J Pathol Inform 2:S1. https://doi.org/10.4103/2153-3539.92027
LeCun Y, Bengio Y, Hinton G (2015) Deep learning. Nature 521:436–444. https://doi.org/10.1038/nature14539
Janowczyk A, Madabhushi A (2016) Deep learning for digital pathology image analysis: a comprehensive tutorial with selected use cases. J Pathol Inform 7:29. https://doi.org/10.4103/2153-3539.186902
Krizhevsky A, Sutskever I, Hinton GE (2017) ImageNet classification with deep convolutional neural networks. Commun ACM 60:84–90. https://doi.org/10.1145/3065386
Bejnordi BE, Zuidhof G, Balkenhol M et al (2017) Context-aware stacked convolutional neural networks for classification of breast carcinomas in whole-slide histopathology images. J Med Imaging Bellingham Wash 4:044504. https://doi.org/10.1117/1.JMI.4.4.044504
Madabhushi A, Agner S, Basavanhally A et al (2011) Computer-aided prognosis: predicting patient and disease outcome via quantitative fusion of multi-scale, multi-modal data. Comput Med Imaging Graph Off J Comput Med Imaging Soc 35:506–514. https://doi.org/10.1016/j.compmedimag.2011.01.008
Lu MY, Williamson DFK, Chen TY et al (2021) Data-efficient and weakly supervised computational pathology on whole-slide images. Nat Biomed Eng 5:555–570. https://doi.org/10.1038/s41551-020-00682-w
Tellez D, Balkenhol M, Otte-Höller I et al (2018) Whole-slide mitosis detection in H E breast histology using PHH3 as a reference to train distilled stain-invariant convolutional networks. IEEE Trans Med Imaging 37:2126–2136. https://doi.org/10.1109/TMI.2018.2820199
Romo-Bucheli D, Janowczyk A, Gilmore H et al (2017) A deep learning based strategy for identifying and associating mitotic activity with gene expression derived risk categories in estrogen receptor positive breast cancers. Cytom Part J Int Soc Anal Cytol 91:566–573. https://doi.org/10.1002/cyto.a.23065
Lu C, Romo-Bucheli D, Wang X et al (2018) Nuclear shape and orientation features from H&E images predict survival in early-stage estrogen receptor-positive breast cancers. Lab Investig J Tech Methods Pathol 98:1438–1448. https://doi.org/10.1038/s41374-018-0095-7
Allison KH, Hammond MEH, Dowsett M et al (2020) Estrogen and progesterone receptor testing in breast cancer: ASCO/CAP guideline update. J Clin Oncol Off J Am Soc Clin Oncol 38:1346–1366. https://doi.org/10.1200/JCO.19.02309
Peck M, Moffat D, Latham B, Badrick T (2018) Review of diagnostic error in anatomical pathology and the role and value of second opinions in error prevention. J Clin Pathol 71:995–1000. https://doi.org/10.1136/jclinpath-2018-205226
Rimm DL, Leung SCY, McShane LM et al (2019) An international multicenter study to evaluate reproducibility of automated scoring for assessment of Ki67 in breast cancer. Mod Pathol Off J U S Can Acad Pathol Inc 32:59–69. https://doi.org/10.1038/s41379-018-0109-4
Rexhepaj E, Brennan DJ, Holloway P et al (2008) Novel image analysis approach for quantifying expression of nuclear proteins assessed by immunohistochemistry: application to measurement of oestrogen and progesterone receptor levels in breast cancer. Breast Cancer Res BCR 10:R89. https://doi.org/10.1186/bcr2187
Tuominen VJ, Ruotoistenmäki S, Viitanen A et al (2010) ImmunoRatio: a publicly available web application for quantitative image analysis of estrogen receptor (ER), progesterone receptor (PR), and Ki-67. Breast Cancer Res BCR 12:R56. https://doi.org/10.1186/bcr2615
Masmoudi H, Hewitt SM, Petrick N et al (2009) Automated quantitative assessment of HER-2/neu immunohistochemical expression in breast cancer. IEEE Trans Med Imaging 28:916–925. https://doi.org/10.1109/TMI.2009.2012901
Hall BH, Ianosi-Irimie M, Javidian P et al (2008) Computer-assisted assessment of the human epidermal growth factor receptor 2 immunohistochemical assay in imaged histologic sections using a membrane isolation algorithm and quantitative analysis of positive controls. BMC Med Imaging 8:11. https://doi.org/10.1186/1471-2342-8-11
Bolton KL, Garcia-Closas M, Pfeiffer RM et al (2010) Assessment of automated image analysis of breast cancer tissue microarrays for epidemiologic studies. Cancer Epidemiol Prev Biomark 19:992–999. https://doi.org/10.1158/1055-9965.EPI-09-1023
Hartage R, Li A, Hammond S, Parwani A (2020) A validation study of human epidermal growth factor receptor 2 immunohistochemistry digital imaging analysis and its correlation with human epidermal growth factor receptor 2 fluorescence In situ hybridization results in breast carcinoma. J Pathol Inform 11:2. https://doi.org/10.4103/jpi.jpi_52_19
Pantanowitz L, Liu C, Huang Y et al (2017) Impact of altering various image parameters on human epidermal growth factor receptor 2 image analysis data quality. J Pathol Inform 8:39. https://doi.org/10.4103/jpi.jpi_46_17
Bui MM, Riben MW, Allison KH et al (2019) Quantitative image analysis of human epidermal growth factor receptor 2 immunohistochemistry for breast cancer: guideline from the College of American Pathologists. Arch Pathol Amp Lab Med 143:1180–1196. https://doi.org/10.5858/arpa.2018-0378-CP
Longacre TA, Ennis M, Quenneville LA et al (2006) Interobserver agreement and reproducibility in classification of invasive breast carcinoma: an NCI breast cancer family registry study. Mod Pathol 19:195–207. https://doi.org/10.1038/modpathol.3800496
Elmore JG, Longton GM, Carney PA et al (2015) Diagnostic concordance among pathologists interpreting breast biopsy specimens. JAMA 313:1122–1132. https://doi.org/10.1001/jama.2015.1405
van Baardwijk A, Bosmans G, Boersma L et al (2007) PET-CT–based auto-contouring in non–small-cell lung cancer correlates with pathology and reduces interobserver variability in the delineation of the primary tumor and involved nodal volumes. Int J Radiat Oncol Biol Phys 68:771–778. https://doi.org/10.1016/j.ijrobp.2006.12.067
Weaver DL (2010) Pathology evaluation of sentinel lymph nodes in breast cancer: protocol recommendations and rationale. Mod Pathol Off J U S Can Acad Pathol Inc 23(Suppl 2):S26–32. https://doi.org/10.1038/modpathol.2010.36
Aresta G, Araújo T, Kwok S et al (2019) BACH: grand challenge on breast cancer histology images. Med Image Anal 56:122–139. https://doi.org/10.1016/j.media.2019.05.010
Polónia A, Campelos S, Ribeiro A et al (2020) Artificial Intelligence improves the accuracy in histologic classification of breast lesions. Am J Clin Pathol. https://doi.org/10.1093/ajcp/aqaa151
Bejnordi BE, Balkenhol M, Litjens G et al (2016) Automated detection of DCIS in whole-slide H E stained breast histopathology images. IEEE Trans Med Imaging 35:2141–2150. https://doi.org/10.1109/TMI.2016.2550620
Radiya-Dixit E, Zhu D, Beck AH (2017) Automated classification of benign and malignant proliferative breast lesions. Sci Rep 7:9900. https://doi.org/10.1038/s41598-017-10324-y
Dong F, Irshad H, Oh E-Y et al (2014) Computational pathology to discriminate benign from malignant intraductal proliferations of the breast. PLoS ONE 9:e114885. https://doi.org/10.1371/journal.pone.0114885
Wetstein SC, Stathonikos N, Pluim JPW et al (2021) Deep learning-based grading of ductal carcinoma in situ in breast histopathology images. Lab Investig J Tech Methods Pathol 101:525–533. https://doi.org/10.1038/s41374-021-00540-6
Cruz-Roa A, Gilmore H, Basavanhally A et al (2017) Accurate and reproducible invasive breast cancer detection in whole-slide images: a deep learning approach for quantifying tumor extent. Sci Rep 7:46450. https://doi.org/10.1038/srep46450
van Rijthoven M, Balkenhol M, Siliņa K et al (2021) HookNet: multi-resolution convolutional neural networks for semantic segmentation in histopathology whole-slide images. Med Image Anal 68:101890. https://doi.org/10.1016/j.media.2020.101890
Kashyap A, Jain M, Shukla S, Andley M (2017) Study of nuclear morphometry on cytology specimens of benign and malignant breast lesions: a study of 122 cases. J Cytol 34:10–15. https://doi.org/10.4103/0970-9371.197591
Osareh A, Shadgar B (2010) Machine learning techniques to diagnose breast cancer. In: 2010 5th International Symposium on Health Informatics and Bioinformatics. IEEE, Ankara, pp 114–120. https://doi.org/10.1109/HIBIT.2010.5478895
Dey P, Logasundaram R, Joshi K (2013) Artificial neural network in diagnosis of lobular carcinoma of breast in fine-needle aspiration cytology. Diagn Cytopathol 41:102–106. https://doi.org/10.1002/dc.21773
Subbaiah RM, Dey P, Nijhawan R (2014) Artificial neural network in breast lesions from fine-needle aspiration cytology smear: ANN of Breast Carcinoma. Diagn Cytopathol 42:218–224. https://doi.org/10.1002/dc.23026
Filipczuk P, Fevens T, Krzyzak A, Monczak R (2013) Computer-aided breast cancer diagnosis based on the analysis of cytological images of fine needle biopsies. IEEE Trans Med Imaging 32:2169–2178. https://doi.org/10.1109/TMI.2013.2275151
Bloom HJ, Richardson WW (1957) Histological grading and prognosis in breast cancer; a study of 1409 cases of which 359 have been followed for 15 years. Br J Cancer 11:359–377. https://doi.org/10.1038/bjc.1957.43
Genestie C, Zafrani B, Asselain B et al (1998) Comparison of the prognostic value of Scarff-Bloom-Richardson and Nottingham histological grades in a series of 825 cases of breast cancer: major importance of the mitotic count as a component of both grading systems. Anticancer Res 18:571–576
Gurcan MN, Boucheron LE, Can A et al (2009) Histopathological image analysis: a review. IEEE Rev Biomed Eng 2:147–171. https://doi.org/10.1109/RBME.2009.2034865
Roux L, Racoceanu D, Loménie N et al (2013) Mitosis detection in breast cancer histological images An ICPR 2012 contest. J Pathol Inform 4.https://doi.org/10.4103/2153-3539.112693
Wang H, Cruz-Roa A, Basavanhally A et al (2014) Mitosis detection in breast cancer pathology images by combining handcrafted and convolutional neural network features. J Med Imaging Bellingham Wash 1:034003. https://doi.org/10.1117/1.JMI.1.3.034003
Veta M, Heng YJ, Stathonikos N et al (2019) Predicting breast tumor proliferation from whole-slide images: the TUPAC16 challenge. Med Image Anal 54:111–121. https://doi.org/10.1016/j.media.2019.02.012
Veta M, van Diest PJ, Willems SM et al (2015) Assessment of algorithms for mitosis detection in breast cancer histopathology images. Med Image Anal 20:237–248. https://doi.org/10.1016/j.media.2014.11.010
Balkenhol MCA, Tellez D, Vreuls W et al (2019) Deep learning assisted mitotic counting for breast cancer. Lab Investig J Tech Methods Pathol 99:1596–1606. https://doi.org/10.1038/s41374-019-0275-0
Pantanowitz L, Hartman D, Qi Y et al (2020) Accuracy and efficiency of an artificial intelligence tool when counting breast mitoses. Diagn Pathol 15:80. https://doi.org/10.1186/s13000-020-00995-z
Criscitiello C, Disalvatore D, De Laurentiis M et al (2014) High Ki-67 score is indicative of a greater benefit from adjuvant chemotherapy when added to endocrine therapy in luminal B HER2 negative and node-positive breast cancer. Breast Edinb Scotl 23:69–75. https://doi.org/10.1016/j.breast.2013.11.007
Polley M-YC, Leung SCY, Gao D et al (2015) An international study to increase concordance in Ki67 scoring. Mod Pathol Off J U S Can Acad Pathol Inc 28:778–786. https://doi.org/10.1038/modpathol.2015.38
Nielsen TO, Leung SCY, Rimm DL et al (2021) Assessment of Ki67 in breast cancer: updated recommendations from the International Ki67 in Breast Cancer Working Group. JNCI J Natl Cancer Inst 113:808–819. https://doi.org/10.1093/jnci/djaa201
Leung SCY, Nielsen TO, Zabaglo L et al (2016) Analytical validation of a standardized scoring protocol for Ki67: phase 3 of an international multicenter collaboration. NPJ Breast Cancer 2:16014. https://doi.org/10.1038/npjbcancer.2016.14
Koopman T, Buikema HJ, Hollema H et al (2018) Digital image analysis of Ki67 proliferation index in breast cancer using virtual dual staining on whole tissue sections: clinical validation and inter-platform agreement. Breast Cancer Res Treat 169:33–42. https://doi.org/10.1007/s10549-018-4669-2
Acs B, Pelekanou V, Bai Y et al (2019) Ki67 reproducibility using digital image analysis: an inter-platform and inter-operator study. Lab Investig J Tech Methods Pathol 99:107–117. https://doi.org/10.1038/s41374-018-0123-7
Plancoulaine B, Laurinaviciene A, Herlin P et al (2015) A methodology for comprehensive breast cancer Ki67 labeling index with intra-tumor heterogeneity appraisal based on hexagonal tiling of digital image analysis data. Virchows Arch Int J Pathol. https://doi.org/10.1007/s00428-015-1865-x
Zilenaite D, Rasmusson A, Augulis R et al (2020) Independent prognostic value of intratumoral heterogeneity and immune response features by automated digital immunohistochemistry analysis in early hormone receptor-positive breast carcinoma. Front Oncol 10:950. https://doi.org/10.3389/fonc.2020.00950
Laurinavicius A, Plancoulaine B, Rasmusson A et al (2016) Bimodality of intratumor Ki67 expression is an independent prognostic factor of overall survival in patients with invasive breast carcinoma. Virchows Arch 468:493–502. https://doi.org/10.1007/s00428-016-1907-z
TNM Classification of Malignant Tumours, 7th edn, Wiley. In: Wiley.com. https://www.wiley.com/en-us/TNM+Classification+of+Malignant+Tumours%2C+7th+Edition-p-9781444358964. Accessed 19 Feb 2021
Vestjens JHMJ, Pepels MJ, de Boer M et al (2012) Relevant impact of central pathology review on nodal classification in individual breast cancer patients. Ann Oncol Off J Eur Soc Med Oncol 23:2561–2566. https://doi.org/10.1093/annonc/mds072
Litjens G, Sánchez CI, Timofeeva N et al (2016) Deep learning as a tool for increased accuracy and efficiency of histopathological diagnosis. Sci Rep 6:26286. https://doi.org/10.1038/srep26286
Ehteshami Bejnordi B, Veta M, Johannes van Diest P et al (2017) Diagnostic assessment of deep learning algorithms for detection of lymph node metastases in women with breast cancer. JAMA 318:2199–2210. https://doi.org/10.1001/jama.2017.14585
Liu Y, Kohlberger T, Norouzi M et al (2019) Artificial intelligence-based breast cancer nodal metastasis detection: insights into the black box for pathologists. Arch Pathol Lab Med 143:859–868. https://doi.org/10.5858/arpa.2018-0147-OA
Bandi P, Geessink O, Manson Q et al (2019) From detection of individual metastases to classification of lymph node status at the patient level: The CAMELYON17 challenge. IEEE Trans Med Imaging 38:550–560. https://doi.org/10.1109/TMI.2018.2867350
Steiner DF, MacDonald R, Liu Y et al (2018) Impact of deep learning assistance on the histopathologic review of lymph nodes for metastatic breast cancer. Am J Surg Pathol 42:1636–1646. https://doi.org/10.1097/PAS.0000000000001151
Wiegand T, Krishnamurthy R, Kuglitsch M et al (2019) WHO and ITU establish benchmarking process for artificial intelligence in health. The Lancet 394:9–11. https://doi.org/10.1016/S0140-6736(19)30762-7
Savas P, Salgado R, Denkert C et al (2016) Clinical relevance of host immunity in breast cancer: from TILs to the clinic. Nat Rev Clin Oncol 13:228–241. https://doi.org/10.1038/nrclinonc.2015.215
Adams S, Diamond JR, Hamilton EP et al (2016) Phase Ib trial of atezolizumab in combination with nab-paclitaxel in patients with metastatic triple-negative breast cancer (mTNBC). J Clin Oncol 34:1009–1009. https://doi.org/10.1200/JCO.2016.34.15_suppl.1009
Nanda R, Chow LQM, Dees EC et al (2016) Pembrolizumab in patients with advanced triple-negative breast cancer: phase Ib KEYNOTE-012 study. J Clin Oncol Off J Am Soc Clin Oncol 34:2460–2467. https://doi.org/10.1200/JCO.2015.64.8931
Denkert C, Loibl S, Noske A et al (2010) Tumor-associated lymphocytes as an independent predictor of response to neoadjuvant chemotherapy in breast cancer. J Clin Oncol Off J Am Soc Clin Oncol 28:105–113. https://doi.org/10.1200/JCO.2009.23.7370
Amgad M, Elfandy H, Hussein H et al (2019) Structured crowdsourcing enables convolutional segmentation of histology images. Bioinformatics 35:3461–3467. https://doi.org/10.1093/bioinformatics/btz083
Amgad M, Sarkar A, Srinivas C et al (2019) Joint region and nucleus segmentation for characterization of tumor infiltrating lymphocytes in breast cancer. Proc SPIE-- Int Soc Opt Eng 10956:109560M. https://doi.org/10.1117/12.2512892
Amgad M, Stovgaard ES, Balslev E et al (2020) Report on computational assessment of Tumor Infiltrating Lymphocytes from the International Immuno-Oncology Biomarker Working Group. NPJ Breast Cancer 6:16. https://doi.org/10.1038/s41523-020-0154-2
Basavanhally AN, Ganesan S, Agner S et al (2010) Computerized image-based detection and grading of lymphocytic infiltration in HER2+ breast cancer histopathology. IEEE Trans Biomed Eng 57:642–653. https://doi.org/10.1109/TBME.2009.2035305
Luen S, Virassamy B, Savas P et al (2016) The genomic landscape of breast cancer and its interaction with host immunity. Breast Edinb Scotl 29:241–250. https://doi.org/10.1016/j.breast.2016.07.015
Rasmusson A, Zilenaite D, Nestarenkaite A et al (2020) Immunogradient indicators for antitumor response assessment by automated tumor-stroma interface zone detection. Am J Pathol 190:1309–1322. https://doi.org/10.1016/j.ajpath.2020.01.018
Saltz J, Gupta R, Hou L et al (2018) Spatial organization and molecular correlation of tumor-infiltrating lymphocytes using deep learning on pathology images. Cell Rep 23:181-193.e7. https://doi.org/10.1016/j.celrep.2018.03.086
Heindl A, Sestak I, Naidoo K et al (2018) Relevance of spatial heterogeneity of immune infiltration for predicting risk of recurrence after endocrine therapy of ER+ breast cancer. JNCI J Natl Cancer Inst 110:166–175. https://doi.org/10.1093/jnci/djx137
Maley CC, Koelble K, Natrajan R et al (2015) An ecological measure of immune-cancer colocalization as a prognostic factor for breast cancer. Breast Cancer Res BCR 17:131. https://doi.org/10.1186/s13058-015-0638-4
Klein ME, Dabbs DJ, Shuai Y et al (2013) Prediction of the Onco type DX recurrence score: use of pathology-generated equations derived by linear regression analysis. Mod Pathol 26:658–664. https://doi.org/10.1038/modpathol.2013.36
Basavanhally A, Jun Xu, Madabhushi A, Ganesan S (2009) Computer-aided prognosis of ER+ breast cancer histopathology and correlating survival outcome with Oncotype DX assay. In: 2009 IEEE International Symposium on Biomedical Imaging: From Nano to Macro. IEEE, Boston, MA, pp 851–854. https://doi.org/10.1109/ISBI.2009.5193186
Romo-Bucheli D, Janowczyk A, Gilmore H et al (2016) Automated tubule nuclei quantification and correlation with oncotype DX risk categories in ER+ Breast Cancer Whole Slide Images. Sci Rep 6:32706. https://doi.org/10.1038/srep32706
Whitney J, Corredor G, Janowczyk A et al (2018) Quantitative nuclear histomorphometry predicts oncotype DX risk categories for early stage ER+ breast cancer. BMC Cancer 18:610. https://doi.org/10.1186/s12885-018-4448-9
Xu Z, Verma A, Naveed U et al (2021) Deep learning predicts chromosomal instability from histopathology images. iScience 24:102394. https://doi.org/10.1016/j.isci.2021.102394
Meti N, Saednia K, Lagree A et al (2021) Machine learning frameworks to predict neoadjuvant chemotherapy response in breast cancer using clinical and pathological features. JCO Clin Cancer Inform 5:66–80. https://doi.org/10.1200/CCI.20.00078
Qu Y, Zhu H, Cao K et al (2020) Prediction of pathological complete response to neoadjuvant chemotherapy in breast cancer using a deep learning (DL) method. Thorac Cancer 11:651–658. https://doi.org/10.1111/1759-7714.13309
Samek W, Müller K-R (2019) Towards explainable artificial intelligence. In: Samek W, Montavon G, Vedaldi A et al (eds) Explainable AI: Interpreting, Explaining and Visualizing Deep Learning. Springer International Publishing, Cham, pp 5–22
Binder A, Bockmayr M, Hägele M et al (2021) Morphological and molecular breast cancer profiling through explainable machine learning. Nat Mach Intell 3:355–366. https://doi.org/10.1038/s42256-021-00303-4
Ja R, Ml G, Pl F et al (2013) A call to standardize preanalytic data elements for biospecimens. Arch Pathol Lab Med 138:526–537. https://doi.org/10.5858/arpa.2013-0250-cp
Rawat RR, Ortega I, Roy P et al (2020) Deep learned tissue “fingerprints” classify breast cancers by ER/PR/Her2 status from H&E images. Sci Rep 10:7275. https://doi.org/10.1038/s41598-020-64156-4
Naik N, Madani A, Esteva A et al (2020) Deep learning-enabled breast cancer hormonal receptor status determination from base-level H&E stains. Nat Commun 11:5727. https://doi.org/10.1038/s41467-020-19334-3
Anand D, Kurian N, Dhage S et al (2020) Deep learning to estimate human epidermal growth factor receptor 2 status from hematoxylin and eosin-stained breast tissue images. J Pathol Inform 11:19. https://doi.org/10.4103/jpi.jpi_10_20
Shamai G, Binenbaum Y, Slossberg R et al (2019) Artificial intelligence algorithms to assess hormonal status from tissue microarrays in patients with breast cancer. JAMA Netw Open 2:e197700. https://doi.org/10.1001/jamanetworkopen.2019.7700
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The paper was conceived by Stuart Schnitt, outline developed by Liron Pantanowitz, first draft written by Mustafa Yousif, and all authors reviewed the draft and contributed equally to the final version of the paper.
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Paul J. van Diest serves on the scientific advisory of Sectra (non-paid). Arvydas Laurinavicius is an independent scientific advisor (non-paid) to the portal https://pathologynews.com/, and a co-author on international patent application (no commercial interest). Anant Madabhushi is an equity holder in Elucid Bioimaging and in Inspirata Inc. In addition, Madabhushi has served as a scientific advisory board member for Inspirata Inc., Astrazeneca, Bristol Meyers-Squibb, and Merck. Currently, he serves on the advisory board of Aiforia Inc., has sponsored research agreements with Philips, AstraZeneca, Boehringer-Ingelheim, and Bristol Meyers-Squibb. Madabhushi’s technology has been licensed to Elucid Bioimaging and he is also involved in a NIH U24 grant with PathCore Inc, and 3 different R01 grants with Inspirata Inc. Liron Pantanowitz is on the scientific advisory board for Ibex and NTP and serves as a consultant for Hamamatsu. David L. Rimm has served as an advisor for Astra Zeneca, Agendia, Amgen, BMS, Cell Signaling Technology, Cepheid, Danaher, Daiichi Sankyo, Konica Minolta, Merck, NanoString, PAIGE.AI, Perkin Elmer, Roche, Sanofi, Ventana, and Ultivue. Amgen, Cepheid, NavigateBP, NextCure, and Konica Minolta fund research in David L. Rimm’s lab. Stuart J. Schnitt is on the scientific advisory boards of PathAI and Ibex. Jeroen van der Laak is a member of the advisory boards of Philips, The Netherlands, and ContextVision, Sweden, and received research funding from Philips, The Netherlands; ContextVision, Sweden; and Sectra, Sweden in the last five years.
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Yousif, M., van Diest, P.J., Laurinavicius, A. et al. Artificial intelligence applied to breast pathology. Virchows Arch 480, 191–209 (2022). https://doi.org/10.1007/s00428-021-03213-3
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DOI: https://doi.org/10.1007/s00428-021-03213-3