Evidence map›Paper›PMID 36816095›Full record

ArticleIEEE journal of translational engineering in health and medicine2023

Automated Molecular Subtyping of Breast Carcinoma Using Deep Learning Techniques.

S Niyas, Ramya Bygari, Rachita Naik, Bhavishya Viswanath, Dhananjay Ugwekar, Tojo Mathew, J Kavya, Jyoti R Kini, Jeny Rajan

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Article in IEEE journal of translational engineering in health and medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

S NiyasDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.ORCID 0000-0001-7319-7156
Ramya BygariDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.
Rachita NaikDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.
Bhavishya ViswanathDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.
Dhananjay UgwekarDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.ORCID 0000-0002-2403-9095
Tojo MathewDepartment of Computer Science and EngineeringThe National Institute of Engineering Mysuru 570008 India.ORCID 0000-0002-7687-9184
J KavyaDepartment of Pathology, Kasturba Medical College, MangaloreManipal Academy of Higher Education Manipal 576104 India.
Jyoti R KiniDepartment of Pathology, Kasturba Medical College, MangaloreManipal Academy of Higher Education Manipal 576104 India.ORCID 0000-0002-3351-9517
Jeny RajanDepartment of Computer Science and EngineeringNational Institute of Technology Karnataka Surathkal 575025 India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMolecular subtyping is an important procedure for prognosis and targeted therapy of breast carcinoma, the most common type of malignancy affecting women. Immunohistochemistry (IHC) analysis is the widely accepted method for molecular subtyping. It involves the assessment of the four molecular biomarkers namely estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and antigen Ki67 using appropriate antibody reagents. Conventionally, these biomarkers are assessed manually by a pathologist, who finally combines individual results to identify the molecular subtype. Molecular subtyping necessitates the status of all the four biomarkers together, and to the best of our knowledge, no such automated method exists. This paper proposes a novel deep learning framework for automatic molecular subtyping of breast cancer from IHC images. METHODS AND PROCEDURES: A modified LadderNet architecture is proposed to segment the immunopositive elements from ER, PR, HER2, and Ki67 biomarker slides. This architecture uses long skip connections to pass encoder feature space from different semantic levels to the decoder layers, allowing concurrent learning with multi-scale features. The entire architecture is an ensemble of multiple fully convolutional neural networks, and learning pathways are chosen adaptively based on input data. The segmentation stage is followed by a post-processing stage to quantify the extent of immunopositive elements to predict the final status for each biomarker.

resultsThe performance of segmentation models for each IHC biomarker is evaluated qualitatively and quantitatively. Furthermore, the biomarker prediction results are also evaluated. The results obtained by our method are highly in concordance with manual assessment by pathologists. CLINICAL IMPACT: Accurate automated molecular subtyping can speed up this pathology procedure, reduce pathologists' workload and associated costs, and facilitate targeted treatment to obtain better outcomes.

Indexed as

Breast NeoplasmsDeep LearningFemaleHumansImmunohistochemistryKi-67 AntigenReceptors, EstrogenKi-67 AntigenReceptors, Estrogenbreast cancerdeep learningimage segmentationMolecular subtyping

Identifiers

PMID36816095
PMCPMC9924555

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.