Scheffel Rafael Selbach, de Cristo Ana Patrícia, Romitti Mirian, Vargas Carla Vaz Ferreira, Ceolin Lucieli, Zanella André B, Dora Jose Miguel, Maia Ana Luiza
Unidade de Tireoide, Hospital de Clínicas de Porto Alegre, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil.
Departamento de Farmacologia, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil.
Arch Endocrinol Metab. 2021 May 18;64(6):751-757. doi: 10.20945/2359-3997000000285.
Although the prognostic role of BRAF mutation in papillary thyroid carcinoma (PTC) is controversial, the American Thyroid Association (ATA) includes the mutational status in their risk stratification system. To evaluate the impact of the BRAF mutation status on PTC risk stratification.
PTC patients attending a university-based hospital who had the analysis of the BRAF mutation were included. Persistent disease was defined as the presence of biochemical or structural disease. The performance of the ATA risk stratification system on predicting persistent disease with or without the BRAF mutation status information was evaluated.
Of the 134 patients evaluated, 44 (32.8%) carried BRAF mutation. The median tumor size was 1.7 cm (P25-75 1.0-3.0), 64 (47.8%) patients had lymph node, and 11 (8.2%) distant metastases. According to the ATA risk stratification system, patients were classified as low, intermediate, and high risk in 55 (41%), 59 (44%), and 20 (14%) patients, respectively. The data on BRAF mutation reclassified 12 (8.9%) patients from low to intermediate risk. After a median follow-up of 8.5 years, the prevalence of persistent disease was similar in patients with and without BRAF mutation (P = 0.42). Multivariate analysis failed to demonstrate an association between the BRAF mutation and persistent disease status (RR 0.96; 95%CI 0.47-1.94). Notably, none of the patients reclassified from low to intermediate risk showed persistent disease on follow-up.
Inclusion of BRAF mutational status has a limited impact on risk stratification and does not add to the prediction of outcomes in PTC patients.
尽管BRAF突变在甲状腺乳头状癌(PTC)中的预后作用存在争议,但美国甲状腺协会(ATA)将突变状态纳入其风险分层系统。旨在评估BRAF突变状态对PTC风险分层的影响。
纳入在一家大学附属医院接受BRAF突变分析的PTC患者。持续性疾病定义为存在生化或结构性疾病。评估了ATA风险分层系统在有无BRAF突变状态信息的情况下预测持续性疾病的性能。
在评估的134例患者中,44例(32.8%)携带BRAF突变。肿瘤中位大小为1.7 cm(P25 - 75 1.0 - 3.0),64例(47.8%)患者有淋巴结转移,11例(8.2%)有远处转移。根据ATA风险分层系统,患者分别被分类为低风险、中风险和高风险,各有55例(41%)、59例(44%)和20例(14%)。BRAF突变数据将12例(8.9%)患者从低风险重新分类为中风险。中位随访8.5年后,有BRAF突变和无BRAF突变患者的持续性疾病患病率相似(P = 0.42)。多因素分析未能证明BRAF突变与持续性疾病状态之间存在关联(风险比0.96;95%置信区间0.47 - 1.94)。值得注意的是,从低风险重新分类为中风险的患者在随访中均未出现持续性疾病。
纳入BRAF突变状态对风险分层的影响有限,且不能增加对PTC患者预后的预测。