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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-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Bioscientifica Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6240143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
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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