Evidence map›Paper›PMID 36768841›Full record

ArticleInternational journal of molecular sciences2023

Annotation-Free Deep Learning-Based Prediction of Thyroid Molecular Cancer Biomarker BRAF (V600E) from Cytological Slides.

Ching-Wei Wang, Hikam Muzakky, Yu-Ching Lee, Yi-Jia Lin, Tai-Kuang Chao

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ching-Wei WangGraduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.ORCID 0000-0001-9992-6863
Hikam MuzakkyGraduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.
Yu-Ching LeeGraduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.ORCID 0000-0002-9233-1223
Yi-Jia LinDepartment of Pathology, Tri-Service General Hospital, Taipei 106335, Taiwan.ORCID 0000-0002-8073-8659
Tai-Kuang ChaoDepartment of Pathology, Tri-Service General Hospital, Taipei 106335, Taiwan.ORCID 0000-0001-8219-6382

Funding

Ministry of Science and Technology, Taiwan MOST 109-2221-E-011-018-MY3, MOST 111-2321-B-016-003National Taiwan University of Science and Technology - Tri-Service General Hospital NTUST-TSGH-112-02Tri-Service General Hospital, Taipei, Taiwan TSGH-D-110036, TSGH-A-111010, and TSGH-A-112008
6 · The paper itself

Abstract

Thyroid cancer is the most common endocrine cancer. Papillary thyroid cancer (PTC) is the most prevalent form of malignancy among all thyroid cancers arising from follicular cells. Fine needle aspiration cytology (FNAC) is a non-invasive method regarded as the most cost-effective and accurate diagnostic method of choice in diagnosing PTC. Identification of BRAF (V600E) mutation in thyroid neoplasia may be beneficial because it is specific for malignancy, implies a worse prognosis, and is the target for selective BRAF inhibitors. To the authors' best knowledge, this is the first automated precision oncology framework effectively predict BRAF (V600E) immunostaining result in thyroidectomy specimen directly from Papanicolaou-stained thyroid fine-needle aspiration cytology and ThinPrep cytological slides, which is helpful for novel targeted therapies and prognosis prediction. The proposed deep learning (DL) framework is evaluated on a dataset of 118 whole slide images. The results show that the proposed DL-based technique achieves an accuracy of 87%, a precision of 94%, a sensitivity of 91%, a specificity of 71% and a mean of sensitivity and specificity at 81% and outperformed three state-of-the-art deep learning approaches. This study demonstrates the feasibility of DL-based prediction of critical molecular features in cytological slides, which not only aid in accurate diagnosis but also provide useful information in guiding clinical decision-making in patients with thyroid cancer. With the accumulation of data and the continuous advancement of technology, the performance of DL systems is expected to be improved in the near future. Therefore, we expect that DL can provide a cost-effective and time-effective alternative tool for patients in the era of precision oncology.

Indexed as

Carcinoma, PapillaryDeep LearningThyroid NeoplasmsBiomarkers, TumorDNA Mutational AnalysisHumansMutationPrecision MedicineProto-Oncogene Proteins B-rafThyroid Cancer, PapillaryBiomarkers, TumorBRAF protein, humanProto-Oncogene Proteins B-rafBRAF (V600E) predictionCLAMdeep learningfine needle aspiration cytologymultiple instance learningpapillary thyroid cancerprecision oncologyweakly supervised

Identifiers

PMID36768841
PMCPMC9916807

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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.