Verburg Frederik A, Wiessmann Martin, Neuloh Georg, Mottaghy Felix M, Brockmann Marc-Alexander
Department of Nuclear Medicine, RWTH University Hospital Aachen.
Department of Nuclear Medicine, University Hospital Marburg.
Nuklearmedizin. 2019 Feb;58(1):23-27. doi: 10.1055/a-0802-5039. Epub 2019 Feb 15.
Here we describe the results of superselective intraarterial application of diagnostic Ga-68-DOTA0,Tyr3-octreotate (Ga-68-DOTATATE) in a series of patients with inoperable WHO grade II meningiomas which were no longer amenable to radiotherapy.
Four patients with inoperable WHO grade II meningioma underwent systemic venous infusion of Ga-68-DOTATATE followed by PET/CT. Ga-68-DOTATATE application was repeated intraarterially via transfemoral catheterization of vessels supplying the meningioma and another PET/CT was performed.
Selective arterial infusion of Ga-68-DOTATATE increased the median value for the maximum standardized uptake value (SUV) by 2.6-fold (median venous: 7.1, median arterial: 21.6; range 2.0-5.0) and the median value for mean SUV by 2.7-fold (median venous: 4.3, median arterial: 11.2; range 1.6-5.6) compared to systemic intravenous infusion. Arterial application was well tolerated by all patients without complications. When compared to liver uptake, intravenous tracer uptake was insufficient for PRRT, whereas tracer uptake after superselective intraarterial tracer injection was sufficient to allow for peptide receptor radionuclide therapy (PRRT) in all patients.
Insufficient tracer uptake in meningiomas after intravenous application of Ga-68-DOTATATE may be safely increased by a factor of 2-5 using transfemoral selective intraarterial tracer application.
在此我们描述了对一系列无法手术切除且不再适合放疗的世界卫生组织(WHO)二级脑膜瘤患者进行超选择性动脉内应用诊断性镓 - 68 - 多胺基多乙酸 - 0,酪胺酸3 - 奥曲肽(Ga - 68 - 多胺基多乙酸 - 奥曲肽)的结果。
4例无法手术切除的WHO二级脑膜瘤患者先进行Ga - 68 - 多胺基多乙酸 - 奥曲肽的全身静脉输注,随后进行PET/CT检查。通过经股动脉插管对供应脑膜瘤的血管进行动脉内重复应用Ga - 68 - 多胺基多乙酸 - 奥曲肽,之后再进行一次PET/CT检查。
与全身静脉输注相比,Ga - 68 - 多胺基多乙酸 - 奥曲肽的选择性动脉内输注使最大标准化摄取值(SUV)的中位数增加了2.6倍(静脉输注中位数:7.1,动脉输注中位数:21.6;范围2.0 - 5.0),平均SUV的中位数增加了2.7倍(静脉输注中位数:4.3,动脉输注中位数:11.2;范围1.6 - 5.6)。所有患者对动脉内应用耐受性良好,无并发症。与肝脏摄取相比,静脉注射示踪剂摄取量不足以进行肽受体放射性核素治疗(PRRT),而超选择性动脉内注射示踪剂后的摄取量足以使所有患者进行肽受体放射性核素治疗(PRRT)。
通过经股动脉选择性动脉内注射示踪剂,可安全地将静脉注射Ga - 68 - 多胺基多乙酸 - 奥曲肽后脑膜瘤中示踪剂摄取不足的情况提高2至5倍。