Afreen Karimkhan MD, Rong Xia MD, PhD, DeAnna Diaz DO, Abigail Wald PhD, Steven Hodak MD, Babak Givi MD, Samer Khader MD, Liron Pantanowitz MD, PhD, MHA, Xiaoying Liu MD, MS, Tamar C. Brandler MD, MS
{"title":"Bethesda III/IV甲状腺细胞学样本中的DICER1突变:一项多中心观察研究","authors":"Afreen Karimkhan MD, Rong Xia MD, PhD, DeAnna Diaz DO, Abigail Wald PhD, Steven Hodak MD, Babak Givi MD, Samer Khader MD, Liron Pantanowitz MD, PhD, MHA, Xiaoying Liu MD, MS, Tamar C. Brandler MD, MS","doi":"10.1002/cncy.70045","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Mutations in <i>DICER1</i> are uncommon, poorly understood, and infrequently found in thyroid nodules.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>The objective of this study was to investigate category III/IV thyroid nodules according to The Bethesda System for Reporting Thyroid Cytopathology with <i>DICER1</i> gene mutations detected in fine-needle aspiration cytology samples using ThyroSeq v3 molecular testing, with a focus on an exploration of the clinical and histopathologic outcomes of these nodules. In this multicenter study spanning more than 6 years, nodules were retrospectively analyzed for patient demographics, clinical course, cytologic features, and histopathology, where available.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>In total, 88 patients with somatic <i>DICER1</i> mutations were included, with a mean age of 39.6 years and a female predominance. All mutations were in the somatic hotspot region, most commonly at the codon 5437 site. Most excised nodules showed benign histologic features (65.9%). Interestingly, the rate of malignancy was higher in this cohort compared with that in the national average.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p><i>DICER1</i> mutations appear to confer a higher risk of malignancy, but are not associated with any specific cytological or histopathological distinguishing features.</p>\n </section>\n </div>","PeriodicalId":9410,"journal":{"name":"Cancer Cytopathology","volume":"133 10","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"DICER1 mutations in Bethesda III/IV thyroid cytology samples: A multicenter observational study\",\"authors\":\"Afreen Karimkhan MD, Rong Xia MD, PhD, DeAnna Diaz DO, Abigail Wald PhD, Steven Hodak MD, Babak Givi MD, Samer Khader MD, Liron Pantanowitz MD, PhD, MHA, Xiaoying Liu MD, MS, Tamar C. Brandler MD, MS\",\"doi\":\"10.1002/cncy.70045\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Mutations in <i>DICER1</i> are uncommon, poorly understood, and infrequently found in thyroid nodules.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>The objective of this study was to investigate category III/IV thyroid nodules according to The Bethesda System for Reporting Thyroid Cytopathology with <i>DICER1</i> gene mutations detected in fine-needle aspiration cytology samples using ThyroSeq v3 molecular testing, with a focus on an exploration of the clinical and histopathologic outcomes of these nodules. In this multicenter study spanning more than 6 years, nodules were retrospectively analyzed for patient demographics, clinical course, cytologic features, and histopathology, where available.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>In total, 88 patients with somatic <i>DICER1</i> mutations were included, with a mean age of 39.6 years and a female predominance. All mutations were in the somatic hotspot region, most commonly at the codon 5437 site. Most excised nodules showed benign histologic features (65.9%). 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DICER1 mutations in Bethesda III/IV thyroid cytology samples: A multicenter observational study
Background
Mutations in DICER1 are uncommon, poorly understood, and infrequently found in thyroid nodules.
Methods
The objective of this study was to investigate category III/IV thyroid nodules according to The Bethesda System for Reporting Thyroid Cytopathology with DICER1 gene mutations detected in fine-needle aspiration cytology samples using ThyroSeq v3 molecular testing, with a focus on an exploration of the clinical and histopathologic outcomes of these nodules. In this multicenter study spanning more than 6 years, nodules were retrospectively analyzed for patient demographics, clinical course, cytologic features, and histopathology, where available.
Results
In total, 88 patients with somatic DICER1 mutations were included, with a mean age of 39.6 years and a female predominance. All mutations were in the somatic hotspot region, most commonly at the codon 5437 site. Most excised nodules showed benign histologic features (65.9%). Interestingly, the rate of malignancy was higher in this cohort compared with that in the national average.
Conclusions
DICER1 mutations appear to confer a higher risk of malignancy, but are not associated with any specific cytological or histopathological distinguishing features.
期刊介绍:
Cancer Cytopathology provides a unique forum for interaction and dissemination of original research and educational information relevant to the practice of cytopathology and its related oncologic disciplines. The journal strives to have a positive effect on cancer prevention, early detection, diagnosis, and cure by the publication of high-quality content. The mission of Cancer Cytopathology is to present and inform readers of new applications, technological advances, cutting-edge research, novel applications of molecular techniques, and relevant review articles related to cytopathology.