NTRK Fusion in a Cohort of BRAF p. V600E Wild-Type Papillary Thyroid Carcinomas

被引:6
|
作者
Lee, Seung Eun [1 ]
Lee, Mi-Sook [2 ,3 ]
Bang, Heejin [1 ]
Kim, Mi Young [4 ]
Choi, Yoon-La [2 ,3 ,5 ]
Oh, Young Lyun [5 ]
机构
[1] Konkuk Univ, Konkuk Univ Med Ctr, Dept Pathol, Sch Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Samsung Med Ctr, Lab Mol Pathol & Theranost, Sch Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Dept Hlth Sci & Technol, SAIHST, Seoul, South Korea
[4] Konkuk Univ, Konkuk Univ Med Ctr, Dept Radiol, Sch Med, Seoul, South Korea
[5] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol & Translat Genom, Sch Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
NTRK fusion; pan-TRK immunohistochemistry; papillary thyroid carcinoma (PTC); TRK inhibitors; RNA-based NGS assay; HIGH PREVALENCE; ONCOGENES; LANDSCAPE; EFFICACY;
D O I
10.1016/j.modpat.2023.100180
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Owing to the availability of a potent tropomyosin receptor kinase (TRK) inhibitor, it is necessary to develop an effective strategy to identify an enriched population of NTRK fusions in papillary thyroid carcinoma (PTC) in routine diagnostic practice. The reported prevalence of NTRK fusion in a large cohort of PTC is similar to 3%. We performed an analysis to refine the characteristic histologic features of PTCs harboring NTRK fusions and further validate the diagnostic utility of pan-TRK immunohistochemistry as a screening tool. In this study, 450 PTCs known to harbor no BRAF p. V600E mutations were screened by pan-TRK immunohistochemistry, and the cases with TRK expression were confirmed by RNA-based next-generation sequencing assay. Eleven NTRK fusion cases were detected (2.4%), and all PTCs were classical subtypes. NTRK1 and NTRK3 were involved in the fusion with 9 different partner genes. Most cases showed similar characteristic histologic findings. Nodular permeative border, multinodular growth with a predominantly follicular pattern, extensive lymphatic invasion, and prominent internodular and intratumoral fibrosis were the characteristic histologic features of NTRK-rearranged PTCs. The ill-defined margins in the ultrasonography findings, which could not be clearly distinguished from the adjacent nontumorous thyroid tissue, were nodular permeative margins in histologic findings. Therefore, preoperative ultrasonographic findings in nodule margins were consistent with the final histologic findings. NTRK1/3 fusion in PTCs showed an overall sensitivity of 100% (95% CI, 71.51%-100%) and specificity of 100% (95% CI, 71.51%-10 0%) in the 22 cases examined, as confirmed with next-generation sequencing. Our study provides an integrative report of the preoperative ultrasonographic, histologic, immunohistochemical, and molecular features of NTRK-rearranged PTCs. Based on these findings, we propose an algorithmic approach for the stepwise assessment of NTRK fusions in PTCs.(c) 2023 United States & Canadian Academy of Pathology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] BRAF V600E in Pediatric Papillary Thyroid Carcinomas
    Paulson, V. A.
    Hollowell, M. L.
    Huang, S. A.
    Barletta, J. A.
    LABORATORY INVESTIGATION, 2014, 94 : 157A - 157A
  • [2] BRAF V600E in Pediatric Papillary Thyroid Carcinomas
    Paulson, V. A.
    Hollowell, M. L.
    Huang, S. A.
    Barletta, J. A.
    MODERN PATHOLOGY, 2014, 27 : 157A - 157A
  • [3] BRAF overexpression is associated with BRAF V600E mutation in papillary thyroid carcinomas
    da Silva, R. C.
    de Paula, H. S. C.
    Leal, C. B. Q. S.
    Cunha, B. C. R.
    de Paula, E. C.
    Alencar, R. C. G.
    Meneghini, A. J.
    Silva, A. M. T. C.
    Gontijo, A. P.
    Wastowski, I. J.
    Saddi, V. A.
    GENETICS AND MOLECULAR RESEARCH, 2015, 14 (02) : 5065 - 5075
  • [4] The landscape and genomic characteristics in BRAF V600E wild type papillary thyroid carcinoma
    Fang, M-Y.
    Xu, C.
    Wang, W-X.
    Wu, M-J.
    Chen, G.
    Ge, M-H.
    ANNALS OF ONCOLOGY, 2018, 29 : 120 - 120
  • [5] Diagnostic significance of the BRAF V600E mutation in conventional papillary thyroid carcinomas
    Zhang, Bo
    Xu, Chun-Wei
    Wu, Yong-Fang
    Man, Qiu-Hong
    Song, Ye-Ying
    Wang, Jing-Jing
    Wang, Huai-Tao
    Wang, Hai-Yan
    Li, Xiao-Bing
    Zhang, Hao
    Ye, Ting
    Zhang, Zhe
    Cai, Cong-Li
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2016, 9 (05): : 8296 - 8303
  • [6] Papillary thyroid carcinomas with and without BRAF? V600E mutations are morphologically distinct
    Finkelstein, Alexander
    Levy, Gillian H.
    Hui, Pei
    Prasad, Avinash
    Virk, Renu
    Chhieng, David C.
    Carling, Tobias
    Roman, Sanziana A.
    Sosa, Julie A.
    Udelsman, Robert
    Theoharis, Constantine G.
    Prasad, Manju L.
    HISTOPATHOLOGY, 2012, 60 (07) : 1052 - 1059
  • [7] Identification of differentially expressed proteins in papillary thyroid carcinomas with V600E mutation of BRAF
    Puxeddu, Efisio
    Susta, Federica
    Orvietani, Pier Luigi
    Chiasserini, Davide
    Barbi, Flavia
    Moretti, Sonia
    Cavaliere, Antonio
    Santeusanio, Fausto
    Avenia, Nicola
    Binaglia, Luciano
    PROTEOMICS CLINICAL APPLICATIONS, 2007, 1 (07) : 672 - 680
  • [8] P53 protein expression, BRAF(V600E) mutation and their clinicopathologic significance in papillary thyroid carcinomas
    Shin, Mi Kyung
    Kim, Jeong Won
    Min, Soo Kee
    Lee, Dong Jin
    Kim, Jin Hwan
    Lee, Seung Chul
    Chung, Bong Wha
    Ju, Young Su
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2014, 34 : S44 - S44
  • [9] BRAF V600E Mutation and Papillary Thyroid Cancer Reply
    Cappola, Anne R.
    Mandel, Susan J.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2013, 310 (05): : 535 - 536
  • [10] BRAF(V600E) mutation and the biology of papillary thyroid cancer
    Frasca, F.
    Nucera, C.
    Pellegriti, G.
    Gangemi, P.
    Attard, M.
    Stella, M.
    Loda, M.
    Vella, V.
    Giordano, C.
    Trimarchi, F.
    Mazzon, E.
    Belfiore, A.
    Vigneri, R.
    ENDOCRINE-RELATED CANCER, 2008, 15 (01) : 191 - 205