1 Department of Surgery, Massachusetts General Hospital , Boston, Massachusetts.
2 Institute for Technology Assessment, Massachusetts General Hospital , Boston, Massachusetts.
Thyroid. 2018 Mar;28(3):328-339. doi: 10.1089/thy.2017.0322. Epub 2018 Feb 27.
BRAF is the most common mutation in papillary thyroid carcinoma (PTC) and can be associated with aggressive disease. Previously, a highly sensitive blood RNA-based BRAF assay was reported. The objective of this study was to assess the correlation of BRAF circulating tumor RNA levels with surgical and medical treatment.
Circulating BRAF levels were assessed in (i) a murine model of undifferentiated (anaplastic) thyroid carcinoma with known BRAF mutation undergoing BRAF-inhibitor (BRAFi) treatment, and (ii) in 111 patients enrolled prior to thyroidectomy (n = 86) or treatment of advanced recurrent or metastatic PTC (n = 25). Blood samples were drawn for BRAF analysis before and after treatment. Testing characteristics were assessed and positivity criteria optimized. Changes in blood BRAF values were assessed and compared to clinical characteristics and response to therapy.
In a murine model of anaplastic thyroid carcinoma with BRAF mutation, blood BRAF RNA correlated with tumor volume in animals treated with BRAFi. In tissue BRAF-positive (n = 36) patients undergoing initial surgery for PTC, blood BRAF levels declined postoperatively (median 370.0-178.5 fg/ng; p = 0.002). In four patients with metastatic or poorly differentiated thyroid carcinoma receiving targeted therapies, blood BRAF declined following therapy and corresponded with radiographic evidence of partial response or stable disease.
This study shows the correlation of blood BRAF levels in response to treatment in both an established animal model of thyroid cancer and in patients with BRAF-positive tumors with all stages of disease. This assay represents an alternative biomarker in patients with positive thyroglobulin antibodies, and tumors, which do not express thyroglobulin.
BRAF 是甲状腺乳头状癌(PTC)中最常见的突变,并且可能与侵袭性疾病相关。此前,有报道称一种高度敏感的基于血液 RNA 的 BRAF 检测方法。本研究的目的是评估 BRAF 循环肿瘤 RNA 水平与手术和药物治疗的相关性。
在(i)已知 BRAF 突变的未分化(间变性)甲状腺癌的小鼠模型中以及(ii)在 111 例甲状腺切除术(n=86)或治疗晚期复发性或转移性 PTC(n=25)之前入组的患者中评估循环 BRAF 水平。在治疗前后采集血液样本进行 BRAF 分析。评估了检测特征,并优化了阳性标准。评估了血液 BRAF 值的变化,并与临床特征和治疗反应进行了比较。
在具有 BRAF 突变的间变性甲状腺癌的小鼠模型中,血液 BRAF RNA 与接受 BRAFi 治疗的动物的肿瘤体积相关。在组织 BRAF 阳性(n=36)接受 PTC 初始手术的患者中,术后血液 BRAF 水平下降(中位数 370.0-178.5 fg/ng;p=0.002)。在接受靶向治疗的四名患有转移性或低分化甲状腺癌的患者中,血液 BRAF 在治疗后下降,与部分缓解或疾病稳定的放射学证据相对应。
本研究显示了在已建立的甲状腺癌动物模型以及 BRAF 阳性肿瘤患者中,治疗反应中血液 BRAF 水平的相关性,这些患者处于疾病的所有阶段。该检测方法代表了对具有阳性甲状腺球蛋白抗体和不表达甲状腺球蛋白的肿瘤的替代生物标志物。