Classic Architecture with Multicentricity and Local Recurrence, and Absence of TERT Promoter Mutations are Correlates of BRAF(V600E) Harboring Pediatric Papillary Thyroid Carcinomas

Onder S., Sari S. O., Yegen G., Sormaz I. C., Yilmaz I., Poyrazoglu S., ...Daha Fazla

ENDOCRINE PATHOLOGY, cilt.27, sa.2, ss.153-161, 2016 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 27 Sayı: 2
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1007/s12022-016-9420-0
  • Dergi Adı: ENDOCRINE PATHOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.153-161
  • Anahtar Kelimeler: Pediatric thyroid cancer, BRAF(V600E), TERT, Papillary thyroid carcinoma, Well differentiated thyroid carcinoma, BRAF V600E, MANAGEMENT GUIDELINES, ADULT PATIENTS, CANCER, FEATURES, CHILDREN, ASSOCIATION, NODULES, DISEASE, RATES
  • İstanbul Üniversitesi Adresli: Evet

Özet

This study is aimed to investigate the BRAF(V600E) and TERT promoter mutation profile of 50 pediatric papillary thyroid carcinomas (PTCs) to refine their clinicopathological correlates. The median age at the time of surgery was 16 years (range, 6-18). No TERT promoter mutations were identified in this series. The BRAF(V600E) mutation was present in 15 (30 %) tumors. From genotype-histologic variant correlation perspective, 13 of 24 classic variant PTCs and 2 of 7 diffuse sclerosing variant PTCs were found to harbor BRAF(V600E) mutation. One cribriform-morular variant, 3 solid variant, and 15 follicular variant PTCs were BRAF wild type. While tumors with distant metastasis were BRAF wild type, two of five tumors with extrathyroidal extension (ETE) harbored BRAF(V600E) mutation. Nine of 15 BRAF(V600E) harboring tumors had central lymph node metastases. There was no significant correlation with BRAF(V600E) mutation and age, gender, tumor size, ETE, central lymph node metastasis, the status of pT, pN1a-b, and distant metastasis. An adverse correlation between BRAF(V600E) mutation and disease-free survival (DFS) was noted in the entire cohort; however, the predictive value of BRAF(V600E) mutation disappeared within the group of tumors displaying classic architecture as well as classic variant PTCs. The present cohort identifies that the classic architecture with multicentricity and local recurrence are correlates of BRAF(V600E) harboring pediatric PTCs. While the small size of this cohort is one of the limitations, neither the BRAF mutation status nor the classic tumor architecture does seem to be an independent prognosticator of DFS in this series. Evidence also suggests that TERT promoter mutations do not seem to play a major role in the pathogenesis of pediatric PTCs.