Evidence map›Paper›PMID 38366204›Full record

ArticleVirchows Archiv : an international journal of pathology2024

Differentiating BRAF V600E- and RAS-like alterations in encapsulated follicular patterned tumors through histologic features: a validation study.

Chankyung Kim, Shipra Agarwal, Andrey Bychkov, Jen-Fan Hang, Agnes Stephanie Harahap, Mitsuyoshi Hirokawa, Kennichi Kakudo, Somboon Keelawat, Chih-Yi Liu, Zhiyan Liu and 5 more

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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  5. BRAF-activated ARSI suppressed EREG-mediated ferroptosis to promote BRAFInternational journal of biological sciences · 2025
    Article
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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

15 authors at 13 institutions in 10 countries.

Chankyung KimDepartment of Anatomical Pathology, SA Pathology, Adelaide, SA, Australia.ORCID https://orcid.org/0000-0001-6054-0605
Shipra AgarwalDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110029, India.ORCID https://orcid.org/0000-0001-7037-4444
Andrey BychkovDepartment of Pathology, Kameda Medical Center, Kamogawa City, Chiba 296-8602, Japan.ORCID https://orcid.org/0000-0002-4203-5696
Jen-Fan HangDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID https://orcid.org/0000-0003-4299-2784
Agnes Stephanie HarahapDepartment of Anatomical Pathology, Faculty of Medicine Universitas Indonesia - Dr. Cipto Mangunkusumo Hospital, Jakarta, Indonesia.ORCID https://orcid.org/0000-0001-8920-7873
Mitsuyoshi HirokawaDepartment of Diagnostic Pathology and Cytology, Kuma Hospital, Kobe, Japan.ORCID https://orcid.org/0000-0001-5558-7142
Kennichi KakudoDepartment of Pathology and Thyroid Disease Center, Izumi City General Hospital, Izumi, Japan.ORCID https://orcid.org/0000-0002-0347-7264
Somboon KeelawatDepartment of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-4180-7914
Chih-Yi LiuDivision of Pathology, Sijhih Cathay General Hospital, New Taipei City, Taiwan.ORCID https://orcid.org/0000-0002-3996-8452
Zhiyan LiuDepartment of Pathology, Sixth People's Hospital, Shanghai Jiao Tong University, Shanghai, China.ORCID https://orcid.org/0000-0001-9668-7756
Truong Phan-Xuan NguyenDepartment of Pathology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-6965-5863
Chanchal RanaDepartment of Pathology, King George Medical University, Lucknow, India.ORCID https://orcid.org/0000-0002-1783-7689
Huy Gia VuongDepartment of Pathology, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.ORCID https://orcid.org/0000-0001-6213-765X
Yun ZhuDepartment of Pathology, Jiangsu Institute of Nuclear Medicine, Wuxi, China.ORCID https://orcid.org/0000-0002-7867-5249
Chan Kwon JungDepartment of Hospital Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea. ckjung@catholic.ac.kr.ORCID http://orcid.org/0000-0001-6843-3708
Chulalongkorn University · THAll India Institute of Medical Sciences · INCathay General Hospital · TWIzumi City General Hospital · JPKameda Medical Center · JPKing George's Medical University · INKuma Hospital · JPShanghai Jiao Tong University · CNSouth Australia Pathology · AUSt. Mary's Hospital · USTaipei Veterans General Hospital · TWUniversity of Indonesia · IDUniversity of Iowa Hospitals and Clinics · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differentiating BRAF V600E- and RAS-altered encapsulated follicular-patterned thyroid tumors based on morphology remains challenging. This study aimed to validate an 8-score scale nuclear scoring system and investigate the importance of nuclear pseudoinclusions (NPIs) in aiding this differentiation. A cohort of 44 encapsulated follicular-patterned tumors with varying degrees of nuclear atypia and confirmed BRAF V600E or RAS alterations was studied. Nuclear parameters (area, diameter, and optical density) were analyzed using a deep learning model. Twelve pathologists from eight Asian countries visually assessed 22 cases after excluding the cases with any papillae. Eight nuclear features were applied, yielding a semi-quantitative score from 0 to 24. A threshold score of 14 was used to distinguish between RAS- and BRAF V600E-altered tumors. BRAF V600E-altered tumors typically demonstrated higher nuclear scores and notable morphometric alterations. Specifically, the nuclear area and diameter were significantly larger, and nuclear optical density was much lower compared to RAS-altered tumors. Observer accuracy varied, with two pathologists correctly identifying genotype of all cases. Observers were categorized into proficiency groups, with the highest group maintaining consistent accuracy across both evaluation methods. The lower group showed a significant improvement in accuracy upon utilizing the 8-score scale nuclear scoring system, with notably increased sensitivity and negative predictive value in BRAF V600E tumor detection. BRAF V600E-altered tumors had higher median total nuclear scores. Detailed reevaluation revealed NPIs in all BRAF V600E-altered cases, but in only 2 of 14 RAS-altered cases. These results could significantly assist pathologists, particularly those not specializing in thyroid pathology, in making a more accurate diagnosis.

Indexed as

Proto-Oncogene Proteins B-rafThyroid NeoplasmsAdenocarcinoma, FollicularAdultAgedBiomarkers, TumorCell NucleusDeep LearningDiagnosis, DifferentialFemaleHumansMaleMiddle AgedMutationObserver VariationPredictive Value of TestsBiomarkers, TumorBRAF protein, humanProto-Oncogene Proteins B-rafras ProteinsBRAFEncapsulated follicular-patterned tumorsMorphometric analysisNuclear featuresPapillary thyroid carcinomaRAS

Identifiers

PMID38366204
OpenAlexW4391885213

What OpenQuestion holds

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Registered trials

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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.