Département d'Imagerie Médicale, Hôpital neuchâtelois, Maladière 45, 2000 Neuchâtel, Switzerland; Department of Nuclear Medicine, Tübingen University Hospital, Otfried-Müller-Strasse 14, 72076 Tübingen, Germany.
Department of Radiology and Nuclear Medicine, Basel University Hospital, Petersgraben 4, 4031 Basel, Switzerland.
Diagn Interv Imaging. 2014 Mar;95(3):289-300. doi: 10.1016/j.diii.2013.07.006. Epub 2013 Sep 12.
PET with (68)Ga-DOTATOC allows for imaging and quantitative assessment of somatostatin receptor expression in neuroendocrine tumors (NET). The aim of this retrospective study was to analyze whether pre-therapeutic (68)Ga-DOTATOC PET/CT is able to predict response to Peptide Receptor Radionuclide Therapy (PRRT).
Forty patients with advanced stage NET were treated with a fixed dose of (90)Y-DOTATOC (5550 or 3700MBq). Prior to PRRT, each patient received (68)Ga-DOTATOC PET/CT. Treatment results were evaluated after 3months by CT, tumor marker levels and clinical course and correlated with (68)Ga-DOTATOC uptake (SUVmax) and the assumed uptake of (90)Y-DOTATOC in tumor manifestations (MBq/g). ROC analysis and pairwise comparison of area under the curve (AUC) were performed with pre-treatment uptake of (68)Ga-DOTATOC, assumed uptake of (90)Y-DOTATOC and treatment activity alone and in relation to body weight as continuous variables, and response/no response as classification variable.
According to conventional criteria (tumor shrinkage, decrease of tumor markers, improved or stable clinical condition), 20 patients were classified as responders, 16 as non-responders and in four patients findings were equivocal. Using a SUV more than 17.9 as cut-off for favorable outcome, PET was able to predict treatment response of all responders and 15 out of 16 non-responders. All four patients with equivocal findings showed SUV less than or equal to 17.9 and soon experienced tumor progression. The assumed uptake of (90)Y-DOTATOC in tumor manifestations using a cut-off more than 1.26MBq/g as predictor of response was able to correctly classify 19 out of 20 responders, and 14 out of 16 non-responders. In all patients with equivocal findings, the assumed uptake of (90)Y-DOTATOC was below 1.26MBq/g.
Pre-therapeutic (68)Ga-DOTATOC tumor uptake as well as assumed uptake of (90)Y-DOTATOC are strongly associated with the results of subsequent PRRT. The defined cut-off values should be confirmed by prospective studies and may then provide the rationale for individual dosing and selecting patients with high likelihood of favorable treatment outcome.
采用 (68)Ga-DOTATOC 正电子发射断层扫描术(PET)可以对神经内分泌肿瘤(NET)中的生长抑素受体表达进行成像和定量评估。本回顾性研究旨在分析治疗前 (68)Ga-DOTATOC PET/CT 是否能够预测肽受体放射性核素治疗(PRRT)的反应。
40 例晚期 NET 患者接受固定剂量的 (90)Y-DOTATOC(5550 或 3700MBq)治疗。在 PRRT 之前,每位患者均接受 (68)Ga-DOTATOC PET/CT 检查。治疗 3 个月后,通过 CT、肿瘤标志物水平和临床过程进行治疗效果评估,并与肿瘤表现中(68)Ga-DOTATOC 摄取(SUVmax)和假设的 (90)Y-DOTATOC 摄取(MBq/g)相关。采用治疗前摄取(68)Ga-DOTATOC、假设摄取(90)Y-DOTATOC 和治疗活性作为连续变量,以及作为分类变量的体重,对 ROC 分析和曲线下面积(AUC)的两两比较进行了分析。
根据常规标准(肿瘤缩小、肿瘤标志物下降、临床状况改善或稳定),20 例患者被归类为有反应者,16 例为无反应者,4 例患者结果不确定。使用 SUV 大于 17.9 作为有利结局的截止值,PET 能够预测所有反应者和 16 名无反应者中的 15 名的治疗反应。4 名结果不确定的患者 SUV 均小于或等于 17.9,且很快出现肿瘤进展。使用假设摄取 (90)Y-DOTATOC 大于 1.26MBq/g 作为反应预测指标,可以正确分类 20 名有反应者中的 19 名和 16 名无反应者中的 14 名。所有结果不确定的患者,(90)Y-DOTATOC 的假设摄取均低于 1.26MBq/g。
治疗前(68)Ga-DOTATOC 肿瘤摄取以及假设摄取(90)Y-DOTATOC 与随后 PRRT 的结果密切相关。所定义的截止值应通过前瞻性研究进行验证,然后可为个体剂量提供依据,并选择具有良好治疗效果可能性的患者。