Department of Nuclear Medicine, the Second Hospital of Shandong University, Jinan, 250033, China.
Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250021, China.
Endocrine. 2024 Apr;84(1):160-170. doi: 10.1007/s12020-023-03564-8. Epub 2023 Oct 18.
The BRAF mutation is the universal genetic mutation in papillary thyroid microcarcinoma (PTMC). The present study is to estimate the role of the BRAF mutation in the clinical outcome of PTMC with intermediate to high recurrence risk after radioactive iodine (RAI) therapy, which is considered to be an indolent tumor.
We conducted a single-center retrospective study. Between May 2016 and March 2019, PTMC patients with known BRAF status who received RAI therapy were reviewed at the Second Hospital of Shandong University. Treatment and follow-up were defined according to criteria used in the 2015 ATA guidelines. The association between the BRAF mutation and clinicopathological characteristics, response to RAI therapy, and recurrence after a period of follow-up were analyzed. Propensity score matching (PSM) and logistic regression were used to control confounding variables.
Of the 322 patients with intermediate to high recurrence risk in PTMC, the mean age of the patients were 43.7 ± 12.2 years, and 72.1% were women. BRAF mutation was found in 64.9% (209/322). After PSM, 112 pairs of patients were matched, and except for multifocality (P = 0.001), extrathyroidal invasion (P = 0.003) and tumor size (P = 0.03), there was no significant difference in all baseline characteristics between the two groups. An excellent response (ER) to RAI therapy was observed in 273 patients (84.7%). At the end of the study, 17(5.2%) and 6(1.8%) patients showed structural incomplete response (SIR) and biochemical incomplete response (BIR) status. The proportion of patients who achieved ER status in the BRAF mutation positive and negative groups was 86.6% and 81.4%, respectively. Kaplan-Meier analyses showed that the BRAF mutation was not related to lower ER reached time. The median follow-up was 51 months.
We found the BRAF mutation was associated with multifocality, extrathyroidal invasion, and tumor size in papillary thyroid microcarcinoma. However, the BRAF mutation had no significant association with clinical outcomes in patients with intermediate to high recurrence risk after RAI therapy. Furthermore, the extra-thyroid uptake results and distant metastasis had been proven to be independent factor predicting the clinical response.
ChiCTR2200062911.
BRAF 突变是甲状腺微小乳头状癌(PTMC)的普遍遗传突变。本研究旨在评估 BRAF 突变在放射性碘(RAI)治疗后具有中高危复发风险的 PTMC 临床结局中的作用,因为这种肿瘤被认为是惰性肿瘤。
我们进行了一项单中心回顾性研究。2016 年 5 月至 2019 年 3 月期间,在山东大学第二医院对已知 BRAF 状态且接受 RAI 治疗的 PTMC 患者进行了回顾性研究。治疗和随访是根据 2015 年 ATA 指南中的标准定义的。分析了 BRAF 突变与临床病理特征、对 RAI 治疗的反应以及随访一段时间后的复发之间的关系。采用倾向评分匹配(PSM)和逻辑回归来控制混杂变量。
在 322 例具有中高危复发风险的 PTMC 患者中,患者的平均年龄为 43.7±12.2 岁,72.1%为女性。BRAF 突变阳性率为 64.9%(209/322)。经过 PSM 后,112 对患者匹配成功,除多灶性(P=0.001)、甲状腺外侵犯(P=0.003)和肿瘤大小(P=0.03)外,两组患者的所有基线特征均无显著差异。273 例(84.7%)患者对 RAI 治疗有良好反应(ER)。研究结束时,17 例(5.2%)和 6 例(1.8%)患者出现结构不完全缓解(SIR)和生化不完全缓解(BIR)状态。BRAF 突变阳性和阴性组患者达到 ER 状态的比例分别为 86.6%和 81.4%。Kaplan-Meier 分析表明,BRAF 突变与较低的 ER 达到时间无关。中位随访时间为 51 个月。
我们发现 BRAF 突变与甲状腺微小乳头状癌的多灶性、甲状腺外侵犯和肿瘤大小有关。然而,BRAF 突变与 RAI 治疗后中高危复发风险患者的临床结局无显著相关性。此外,甲状腺外摄取结果和远处转移已被证明是预测临床反应的独立因素。
ChiCTR2200062911。