Division of Abdominal Imaging and Intervention, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
J Vasc Interv Radiol. 2011 Mar;22(3):354-60. doi: 10.1016/j.jvir.2010.11.027.
To determine if tumor fluorine-18 fluorodeoxyglucose ((18)F-FDG) activity is dissipated by radiofrequency (RF) ablation or cryoablation during tumor ablation guided by positron emission tomography/computed tomography (PET/CT).
This prospective study enrolled 12 patients (9 women and 3 men, 39-65 years old), each with at least one (18)F-FDG-avid liver, perihepatic, or lung tumor. Six patients (experimental group) underwent percutaneous PET/CT-guided RF ablation (n = 3) or cryoablation (n = 3). Six patients (control group) underwent diagnostic PET/CT-guided percutaneous biopsy. At a mean time of 103.5 minutes after a single intravenous (18)F-FDG dose, preprocedure and postprocedure PET/CT scans, separated by a mean time interval of 83.4 minutes, were obtained in all patients. Target tumor maximum standardized uptake value (TSUVmax) and ratio (SUVratio) of TSUVmax to normal liver average standardized uptake value (LSUVavg) were measured on all scans. Percentage changes in TSUVmax and SUVratio from preprocedure to postprocedure scans were compared for both groups and analyzed using the Student t test (P < .05 considered statistically significant).
For all patients in both groups, TSUVmax and SUVratio increased from preprocedure to postprocedure PET/CT scans without statistically significant differences. The mean percentage increase in TSUVmax for the ablation group was 32.5% (range 8.2%-46.7%) and for the biopsy group was 24.6% (3.7%-42.4%; P = .45). The mean percentage increase in SUVratio for the ablation group was 47.9% (18.8%-69.6%) and for the biopsy group was 37.6% (9.4%-65%; P = .37).
Tumor (18)F-FDG activity is not dissipated by percutaneous RF ablation or cryoablation. When performing (18)F-FDG PET/CT-guided RF ablation or cryoablation, changes in target tumor (18)F-FDG activity cannot be used to monitor treatment effects.
在正电子发射断层扫描/计算机断层扫描 (PET/CT) 引导下,通过射频 (RF) 消融或冷冻消融对肿瘤进行消融时,确定肿瘤氟-18 氟脱氧葡萄糖 ((18)F-FDG) 活性是否会消散。
本前瞻性研究纳入了 12 名患者(9 名女性和 3 名男性,年龄 39-65 岁),每位患者均至少有一个 (18)F-FDG 摄取的肝、肝周或肺肿瘤。6 名患者(实验组)接受了经皮 PET/CT 引导下的 RF 消融(n = 3)或冷冻消融(n = 3)。6 名患者(对照组)接受了诊断性 PET/CT 引导下的经皮活检。所有患者在静脉注射 (18)F-FDG 剂量后平均 103.5 分钟,在平均间隔 83.4 分钟后分别获得术前和术后 PET/CT 扫描。所有扫描均测量靶肿瘤最大标准化摄取值 (TSUVmax) 和 TSUVmax 与正常肝平均标准化摄取值 (LSUVavg) 的比值 (SUVratio)。使用学生 t 检验比较两组患者术前与术后扫描的 TSUVmax 和 SUVratio 的百分比变化,并进行统计学分析(P <.05 认为具有统计学意义)。
两组所有患者的 TSUVmax 和 SUVratio 均在术前和术后 PET/CT 扫描中升高,无统计学差异。消融组 TSUVmax 的平均百分比增加为 32.5%(范围 8.2%-46.7%),活检组为 24.6%(3.7%-42.4%;P =.45)。消融组 SUVratio 的平均百分比增加为 47.9%(18.8%-69.6%),活检组为 37.6%(9.4%-65%;P =.37)。
经皮 RF 消融或冷冻消融不会消散肿瘤 (18)F-FDG 活性。在进行 (18)F-FDG PET/CT 引导下的 RF 消融或冷冻消融时,靶肿瘤 (18)F-FDG 活性的变化不能用于监测治疗效果。