Evidence map›Paper›PMID 42260747›Full record

ArticleCancer medicine2026

Preoperative Co-Mutation of BRAF

Chang Deng, Yijia Cao, Yuping Deng, Lin Chun, Su Xinliang

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Chang DengDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID https://orcid.org/0000-0002-1108-9624
Yijia CaoDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID https://orcid.org/0009-0007-6998-9397
Yuping DengDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID https://orcid.org/0009-0009-9402-804X
Lin ChunDepartment of Thyroid and Breast Surgery, Guangyuan Central Hospital, Guangyuan, China.ORCID https://orcid.org/0009-0002-6569-8211
Su XinliangDepartment of Breast and Thyroid Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.ORCID https://orcid.org/0000-0001-5792-1407

Funding

Chongqing Municipal Education Commission KJQN202501121
6 · The paper itself

Abstract

backgroundThe individual prognostic impacts of BRAF

objectiveTo evaluate the clinicopathological features and recurrence risk associated with the combined BRAF

methodsThis retrospective study included 756 PTC patients. Mutations were detected from preoperative fine-needle aspiration (FNA) samples. Patients were stratified into three groups: double wild-type (BRAF-/TERT-, n = 121), BRAF-mutant only (BRAF+/TERT-, n = 606), and both-mutant (BRAF+/TERT+, n = 27). Clinicopathological comparisons used appropriate statistical tests. Risk factors for extrathyroidal extension (ETE) and high nodal burden (NLNM ≥ 5) were analyzed via univariate and multivariate logistic regression. Recurrence-free survival (RFS) was assessed by Kaplan-Meier analysis and log-rank test.

resultsThe BRAF+/TERT+ group exhibited the most aggressive phenotype: older age (mean 55.2 vs. 41.9-42.7 years, p < 0.001), larger tumors (median 20.0 vs. 8.7-9.3 mm, p < 0.001), highest rates of ETE (85.2% vs. 10.7%-14.0%, p < 0.001), and heaviest nodal burden (NLNM ≥ 5: 63.0% vs. 25.4%-31.4%, p < 0.001). In multivariate analysis, the double-mutant status was the strongest independent risk factor for both ETE (OR = 11.35; p < 0.001) and NLNM ≥ 5 (OR = 8.02; p = 0.044). With a median follow-up of 27 months, Kaplan-Meier analysis revealed a significantly inferior RFS for the BRAF+/TERT+ group compared to the others (log-rank p < 0.001). In contrast, the only BRAF-mutant group exhibited fewer aggressive features, primarily associated with a higher body mass index (BMI) and lower prevalence of Hashimoto's thyroiditis.

conclusionBRAF

Indexed as

MutationPromoter Regions, GeneticProto-Oncogene Proteins B-rafTelomeraseThyroid Cancer, PapillaryThyroid NeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalPrognosisRetrospective StudiesBRAF protein, humanProto-Oncogene Proteins B-rafTelomeraseTERT protein, humanBRAF mutationextrathyroidal extensionlymph nodes metastasispapillary thyroid carcinomarecurrence‐free survivalTERT promoter mutation

Identifiers

PMID42260747
PMCPMC13247126

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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.