Evidence map›Paper›PMID 39985045›Full record

ArticleDiagnostic pathology2025

Annotation-free genetic mutation estimation of thyroid cancer using cytological slides from multi-centers.

Siping Xiong, Shuguang Liu, Wei Zhang, Chao Zeng, Degui Liao, Tian Tang, Shimin Wang, Yimin Guo

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Article in Diagnostic pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Siping Xiong *Department of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China.
Shuguang Liu *Department of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China.
Wei Zhang *Department of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China.
Chao ZengDepartment of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China.
Degui LiaoDepartment of Pathology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510000, Guangdong, China.
Tian TangDepartment of Pathology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510000, Guangdong, China. tt9772888@126.com.
Shimin WangDepartment of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China. wangshm35@mail.sysu.edu.cn.
Yimin GuoDepartment of Pathology, The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518000, Guangdong, China. guoym35@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thyroid cancer is the most common form of endocrine malignancy and fine needle aspiration (FNA) cytology is a reliable method for clinical diagnosis. Identification of genetic mutation status has been proved efficient for accurate diagnosis and prognostic risk stratification. In this study, a dataset with thyroid cytological images of 310 indeterminate (TBS3 or 4) and 392 PTC (TBS5 or 6) was collected. We introduced a multimodal cascaded network framework to estimate BARF V600E and RAS mutations directly from thyroid cytological slides. The area under the curve in the external testing set achieved 0.902 ± 0.063 and 0.801 ± 0.137 AUCs for BRAF, and RAS, respectively. The results demonstrated that deep neural networks have the potential in cytologically predicting valuable diagnosis and comprehensive genetic status.

Indexed as

MutationProto-Oncogene Proteins B-rafThyroid Cancer, PapillaryThyroid NeoplasmsAdultBiomarkers, TumorBiopsy, Fine-NeedleDNA Mutational AnalysisFemaleHumansMaleMiddle AgedNeural Networks, ComputerProto-Oncogene Proteins p21(ras)Biomarkers, TumorBRAF protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)Annotation-freeDeep convolutional networkFine needle aspiration cytologyGene mutation estimationThyroid cancer

Identifiers

PMID39985045
PMCPMC11846261

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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.