Evidence map›Paper›PMID 42260972›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2026

BRAF Mutation and Tumor Growth Kinetics during Active Surveillance of Papillary Thyroid Microcarcinoma: A Single-Center Retrospective Study.

Jinyoung Kim, Min Kyoung Lee, Tae-Jung Kim, Dong-Jun Lim, Ki-Hyun Baek

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Article in Endocrinology and metabolism (Seoul, Korea), 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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5 · Who and what money

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5 authors.

Jinyoung Kim *Division of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Min Kyoung Lee *Department of Radiology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Tae-Jung KimDepartment of Hospital Pathology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Dong-Jun LimDivision of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Ki-Hyun BaekDivision of Endocrinology and Metabolism, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. drbkh@catholic.ac.kr.

Funding

Ministry of Education RS-2023-00245534National Research Foundation of Korea
6 · The paper itself

Abstract

backgruoundWe investigated tumor volume doubling time (TVDT) during active surveillance of papillary thyroid microcarcinoma (PTMC) and reviewed clinical factors including BRAF mutation associated with tumor progression.

methodsPatients with PTMC who deferred surgery for more than 1 year after diagnosis between 2014 and 2021 and were followed until 2023 were enrolled. Inclusion criteria were papillary thyroid carcinoma confirmed by fine needle aspiration cytology (Bethesda categories V-VI), maximal tumor diameter ≤1 cm, and available BRAF mutation testing.

resultsA total of 85 patients were included. The median age was 49 years, and 63 patients (74%) were female. The positivity rate for BRAF mutation was 51% in the study cohort, and 16 patients (19%) showed rapid-growing disease, defined by a TVDT of less than 5 years. The median follow-up duration was 4.4 years, and 23 patients (27%) underwent surgery after a median of 3.2 years. When TVDT groups were analyzed using logistic regression, sonographic features with microcalcification were associated with tumor growth in binary regression (odds ratio for the group combining slowly and rapid-growing disease was 4.34; 95% confidence interval [CI], 1.41 to 13.35; P=0.010), and BRAF mutation was associated with rapid-growing disease in multinomial regression (odds ratio for rapid-growing disease was 4.48; 95% CI, 1.08 to 18.51; P=0.038).

conclusionBRAF mutation is presumed to be associated with tumor progression and may predict growth of PTMC. Genetic testing including BRAF testing may help distinguishing rapid-growing thyroid cancer.

Indexed as

Carcinoma, PapillaryMutationProto-Oncogene Proteins B-rafThyroid NeoplasmsWatchful WaitingAdultAgedDisease ProgressionFemaleHumansMaleMiddle AgedRetrospective StudiesTumor BurdenBRAF protein, humanProto-Oncogene Proteins B-rafActive surveillanceBRAF mutationPapillary thyroid cancerTumor volume doubling time

Identifiers

PMID42260972
PMCPMC13341190

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