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用 (90)Y-DOTATOC 进行神经内分泌肿瘤的肽受体放射性核素治疗:(68)Ga-DOTATOC 的预治疗摄取能否预测治疗反应?

Peptide receptor radionuclide therapy of neuroendocrine tumors with (90)Y-DOTATOC: is treatment response predictable by pre-therapeutic uptake of (68)Ga-DOTATOC?

机构信息

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.

出版信息

Diagn Interv Imaging. 2014 Mar;95(3):289-300. doi: 10.1016/j.diii.2013.07.006. Epub 2013 Sep 12.

Abstract

PURPOSE

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).

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

患者和方法

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。

结果

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。

结论

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。

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