<i>TERT</i> promoter–mutated thyroid carcinomas: prognostic and histologic insights according to <scp>the WHO</scp> 2022 classification

AIMS: TERT promoter mutations are late molecular events associated with tumour dedifferentiation and aggressive behaviour in thyroid carcinomas (TCs). Although certain adverse histologic features, particularly tall cell morphology, are enriched in TERT promoter-mutated papillary thyroid carcinoma (PTC), their independent prognostic significance within the American Thyroid Association (ATA) high-risk group remains uncertain. This study aimed to assess its prognostic relevance and characterize the histologic spectrum of TERT promoter-mutated TCs, including differentiated high-grade thyroid carcinoma (DHGTC), to refine risk stratification. METHODS AND RESULTS: We retrospectively analysed 151 TCs harbouring TERT promoter mutations, reclassified according to the WHO 2022 classification, which includes newly defined DHGTC. The low frequency of TERT promoter mutations in PTC (2.4%) likely reflects the reclassification of cases previously diagnosed as PTC to DHGTC. Tall cell morphology remained strongly associated with TERT promoter mutations but did not confer additional prognostic significance within this ATA high-risk group. Furthermore, applying the stricter WHO criteria for TC-PTC (≥3× height criteria) did not enhance risk stratification. Importantly, histologic features indicative of tumour progression, including loss of polarity/cohesiveness and early necrotic change, were frequently observed and significantly associated with aggressive clinicopathologic features. Accordingly, tumours exhibiting these features may not only reflect progression toward high-grade disease but also serve as surrogate histologic indicators of underlying TERT promoter mutations. CONCLUSIONS: Our study provides valuable insights into TERT promoter-mutated TCs, broadening their recognized morphologic spectrum and highlighting the importance of incorporating such features into routine evaluation to improve risk stratification and better identify aggressive tumours.

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Publication Details

Journal
Histopathology
Published
2026-04-17
DOI
https://doi.org/10.1111/his.70152
Primary Topic
Thyroid Cancer Diagnosis and Treatment
Type
article
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article

TERT promoter–mutated thyroid carcinomas: prognostic and histologic insights according to the WHO 2022 classification

Young Lyun Oh, Jung‐Sun Kim, Seung Eun Lee, Bogyeong Han
Histopathology
Thyroid Cancer Diagnosis and Treatment
article

TERT promoter–mutated thyroid carcinomas: prognostic and histologic insights according to the WHO 2022 classification

Young Lyun Oh, Jung‐Sun Kim, Seung Eun Lee, Bogyeong Han
article en

Abstract

AIMS: TERT promoter mutations are late molecular events associated with tumour dedifferentiation and aggressive behaviour in thyroid carcinomas (TCs). Although certain adverse histologic features, particularly tall cell morphology, are enriched in TERT promoter-mutated papillary thyroid carcinoma (PTC), their independent prognostic significance within the American Thyroid Association (ATA) high-risk group remains uncertain. This study aimed to assess its prognostic relevance and characterize the histologic spectrum of TERT promoter-mutated TCs, including differentiated high-grade thyroid carcinoma (DHGTC), to refine risk stratification. METHODS AND RESULTS: We retrospectively analysed 151 TCs harbouring TERT promoter mutations, reclassified according to the WHO 2022 classification, which includes newly defined DHGTC. The low frequency of TERT promoter mutations in PTC (2.4%) likely reflects the reclassification of cases previously diagnosed as PTC to DHGTC. Tall cell morphology remained strongly associated with TERT promoter mutations but did not confer additional prognostic significance within this ATA high-risk group. Furthermore, applying the stricter WHO criteria for TC-PTC (≥3× height criteria) did not enhance risk stratification. Importantly, histologic features indicative of tumour progression, including loss of polarity/cohesiveness and early necrotic change, were frequently observed and significantly associated with aggressive clinicopathologic features. Accordingly, tumours exhibiting these features may not only reflect progression toward high-grade disease but also serve as surrogate histologic indicators of underlying TERT promoter mutations. CONCLUSIONS: Our study provides valuable insights into TERT promoter-mutated TCs, broadening their recognized morphologic spectrum and highlighting the importance of incorporating such features into routine evaluation to improve risk stratification and better identify aggressive tumours.

Histopathology
Samsung Medical Center (KR), Konkuk University Medical Center (KR)
Openalex Percentile: Top 16%
Thyroid Cancer Diagnosis and Treatment
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