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

被引:15
|
作者
Henke, Lauren E. [1 ]
Pfeifer, John D. [2 ]
Baranski, Thomas J. [3 ]
DeWees, Todd [4 ]
Grigsby, Perry W. [1 ,5 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Internal Med, Div Endocrinol Diabet & Metab, St Louis, MO 63110 USA
[4] Mayo Clin, Div Biomed Stat & Informat, Scottsdale, AZ USA
[5] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, Div Nucl Med, St Louis, MO 63130 USA
来源
ENDOCRINE CONNECTIONS | 2018年 / 7卷 / 12期
关键词
classic papillary thyroid carcinoma; follicular variant of papillary thyroid carcinoma; BRAF mutation; C-PTC; FV-PTC; BRAF V600E MUTATION; BRAF(V600E) MUTATION; CANCER; ASSOCIATION; POPULATION; MANAGEMENT; SURVIVAL; FEATURES;
D O I
10.1530/EC-18-0264
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1226 / 1235
页数:10
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