Endocr Pract. 2018 Jan;24(1):21-26. doi: 10.4158/EP-2017-0080. Epub 2017 Nov 16.
Papillary thyroid cancer (PTC) harboring a BRAF gene mutation has been shown to exhibit aggressive tumor behavior and carries higher risks of recurrence and disease-specific death. In this systematic review and meta-analysis, we examined published evidence related to the accuracy of fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) in detection of residual disease in patients with BRAF mutated thyroid cancer.
We extracted data from PUBMED/MEDLINE and EMBASE published between January 1995 and March 2017. We included studies that compared FDG PET standardized uptake values (SUVs) between BRAF-positive and BRAF-negative subjects, as well as those that evaluated the odds of having FDG avidity between BRAF-positive and -negative patients with thyroid cancer.
There were a total of 12 studies in the systematic review. Seven studies qualified for the analysis for calculating the pooled odds ratio (OR). The pooled cohort with binary data had 1,144 patients out of which 843 were BRAF positive and 301 were BRAF negative. Those with a BRAF mutation had a significantly greater likelihood of having FDG-avid lesions. The pooled OR was 2.12 (confidence interval [CI] 1.53-3.00, P<.01). The pooled mean SUV (cohort of 315 patients) was significantly higher in BRAF-positive compared to BRAF negative patients, with a pooled mean difference of 5.1 (CI 4.3-5.8).
Our meta-analysis shows that presence of BRAF mutation in PTC confers a higher likelihood of FDG PET avidity and is associated with higher SUV uptake values compared to BRAF-mutation negative status.
BRAF = B-Raf proto-oncogene, serine/threonine kinase; CI = confidence interval; CT = computed tomography; DTC = differentiated thyroid cancer; FDG = fluorodeoxyglucose; PET = positron emission tomography; PTC = papillary thyroid cancer; SUV = standardized uptake value.
研究表明,携带 BRAF 基因突变的甲状腺乳头状癌(PTC)具有侵袭性肿瘤行为,并且复发和疾病特异性死亡的风险更高。在本系统评价和荟萃分析中,我们检查了有关氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG PET/CT)检测 BRAF 突变型甲状腺癌患者残留疾病的准确性的已发表证据。
我们从 1995 年 1 月至 2017 年 3 月期间在 PUBMED/MEDLINE 和 EMBASE 上提取数据。我们纳入了比较 BRAF 阳性和 BRAF 阴性受试者之间 FDG 标准化摄取值(SUV)的研究,以及评估 BRAF 阳性和阴性甲状腺癌患者之间 FDG 摄取可能性的研究。
系统评价共纳入 12 项研究。有 7 项研究符合分析标准,可计算汇总优势比(OR)。有二进制数据的汇总队列共有 1144 例患者,其中 843 例为 BRAF 阳性,301 例为 BRAF 阴性。具有 BRAF 突变的患者更有可能存在 FDG 摄取病灶。汇总 OR 为 2.12(置信区间[CI] 1.53-3.00,P<.01)。与 BRAF 阴性患者相比,BRAF 阳性患者的 FDG 摄取 SUV(315 例患者的队列)明显更高,汇总平均差异为 5.1(CI 4.3-5.8)。
我们的荟萃分析表明,PTC 中 BRAF 突变的存在使 FDG PET 摄取的可能性更高,并与 BRAF 突变阴性状态相比,与更高的 SUV 摄取值相关。
BRAF = B-Raf 原癌基因,丝氨酸/苏氨酸激酶;CI = 置信区间;CT = 计算机断层扫描;DTC = 分化型甲状腺癌;FDG = 氟脱氧葡萄糖;PET = 正电子发射断层扫描;PTC = 甲状腺乳头状癌;SUV = 标准化摄取值。