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Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma

The majority of papillary thyroid carcinoma (PTC) cases comprise classic papillary (C-PTC) and follicular variant (FV-PTC) histologic sub-types. Historically, clinical equivalency was assumed, but recent data suggest C-PTC may have poorer outcomes. However, large single-institution series with long-...

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Autores principales: Henke, Lauren E, Pfeifer, John D, Baranski, Thomas J, DeWees, Todd, Grigsby, Perry W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240143/
https://www.ncbi.nlm.nih.gov/pubmed/30352402
http://dx.doi.org/10.1530/EC-18-0264
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author Henke, Lauren E
Pfeifer, John D
Baranski, Thomas J
DeWees, Todd
Grigsby, Perry W
author_facet Henke, Lauren E
Pfeifer, John D
Baranski, Thomas J
DeWees, Todd
Grigsby, Perry W
author_sort Henke, Lauren E
collection PubMed
description The majority of papillary thyroid carcinoma (PTC) cases comprise classic papillary (C-PTC) and follicular variant (FV-PTC) histologic sub-types. Historically, clinical equivalency was assumed, but recent data suggest C-PTC may have poorer outcomes. However, large single-institution series with long-term outcomes of C-PTC and FV-PTC, using modern pathologic criteria for FV-PTC, are needed. Our objective was to compare prevalence and impact of clinicopathologic factors, including BRAF mutation status, on long-term outcomes of C-PTC and FV-PTC. We hypothesized that patients with C-PTC would have higher risk disease features and worse survival outcomes. This retrospective study included 1293 patients treated at a single, US academic institution between 1943 and 2009 with mean follow-up of 8.6 years. All patients underwent either partial or total thyroidectomy and had invasive C-PTC or FV-PTC per modern pathology criteria. Primary study measurements included differences in recurrence-free survival (RFS), disease-specific survival (DSS) and associations with clinicopathologic factors including the BRAF mutation. Compared to FV-PTC, C-PTC was associated with multiple features of high-risk disease (P < 0.05) and significantly reduced RFS and DSS. Survival differences were consistent across univariate, multivariate and Kaplan–Meier analyses. BRAF mutations were more common in C-PTC (P = 0.002). However, on Kaplan–Meier analysis, mutational status did not significantly impact RFS or DSS for patients with either histologic sub-type. C-PTC therefore indicates higher-risk disease and predicts for significantly poorer long-term outcomes when compared to FV-PTC. The nature of this difference in outcome is not explained by traditional histopathologic findings or by the BRAF mutation.
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spelling pubmed-62401432018-11-21 Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma Henke, Lauren E Pfeifer, John D Baranski, Thomas J DeWees, Todd Grigsby, Perry W Endocr Connect Research The majority of papillary thyroid carcinoma (PTC) cases comprise classic papillary (C-PTC) and follicular variant (FV-PTC) histologic sub-types. Historically, clinical equivalency was assumed, but recent data suggest C-PTC may have poorer outcomes. However, large single-institution series with long-term outcomes of C-PTC and FV-PTC, using modern pathologic criteria for FV-PTC, are needed. Our objective was to compare prevalence and impact of clinicopathologic factors, including BRAF mutation status, on long-term outcomes of C-PTC and FV-PTC. We hypothesized that patients with C-PTC would have higher risk disease features and worse survival outcomes. This retrospective study included 1293 patients treated at a single, US academic institution between 1943 and 2009 with mean follow-up of 8.6 years. All patients underwent either partial or total thyroidectomy and had invasive C-PTC or FV-PTC per modern pathology criteria. Primary study measurements included differences in recurrence-free survival (RFS), disease-specific survival (DSS) and associations with clinicopathologic factors including the BRAF mutation. Compared to FV-PTC, C-PTC was associated with multiple features of high-risk disease (P < 0.05) and significantly reduced RFS and DSS. Survival differences were consistent across univariate, multivariate and Kaplan–Meier analyses. BRAF mutations were more common in C-PTC (P = 0.002). However, on Kaplan–Meier analysis, mutational status did not significantly impact RFS or DSS for patients with either histologic sub-type. C-PTC therefore indicates higher-risk disease and predicts for significantly poorer long-term outcomes when compared to FV-PTC. The nature of this difference in outcome is not explained by traditional histopathologic findings or by the BRAF mutation. Bioscientifica Ltd 2018-10-08 /pmc/articles/PMC6240143/ /pubmed/30352402 http://dx.doi.org/10.1530/EC-18-0264 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Henke, Lauren E
Pfeifer, John D
Baranski, Thomas J
DeWees, Todd
Grigsby, Perry W
Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title_full Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title_fullStr Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title_full_unstemmed Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title_short Long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
title_sort long-term outcomes of follicular variant vs classic papillary thyroid carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240143/
https://www.ncbi.nlm.nih.gov/pubmed/30352402
http://dx.doi.org/10.1530/EC-18-0264
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