首页> 外文期刊>Cancer Imaging >Changes in biodistribution on 68Ga-DOTA-Octreotate PET/CT after long acting somatostatin analogue therapy in neuroendocrine tumour patients may result in pseudoprogression
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Changes in biodistribution on 68Ga-DOTA-Octreotate PET/CT after long acting somatostatin analogue therapy in neuroendocrine tumour patients may result in pseudoprogression

机译:长效生长抑素类似物治疗神经内分泌肿瘤患者后68Ga-DOTA-奥曲肽PET / CT的生物分布变化可能导致假进展

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BackgroundTo evaluate the effects of long-acting somatostatin analogue (SSA) therapy on 68Ga-DOTA-octreotate (GaTate) uptake at physiological and metastatic sites in neuroendocrine tumour (NET) patients.Go to:MethodsTwenty-one patients who underwent GaTate PET/CT before and after commencement of SSA therapy were reviewed. Maximum standardized uptake values (SUVmax) were measured in normal organs. Changes in uptake of 49 metastatic lesions in 12 patients with stable disease were also compared. Serum chromogranin-A (CgA) levels were available for correlation between scans in 17/21 patients.Go to:ResultsMean thyroid, spleen and liver SUVmax decreased significantly following SSA therapy from a baseline of 5.9 to 3.5, 30.3 to 23.1 and 10.3 to 8.0, respectively (p?=?
机译:背景为了评估长效生长抑素类似物(SSA)治疗对神经内分泌肿瘤(NET)患者生理和转移部位68Ga-DOTA-奥曲肽(GaTate)吸收的影响。方法:21例接受GaTate PET / CT的患者在开始SSA治疗之前和之后进行了回顾。在正常器官中测量最大标准化摄取值(SUVmax)。还比较了12例疾病稳定患者中49个转移灶的摄取变化。血清嗜铬粒蛋白A(CgA)水平可用于17/21患者的各次扫描之间的相关性。转到:结果SSA治疗后,平均甲状腺,脾脏和肝脏SUVmax明显降低,从基线的5.9降至3.5、30.3的23.1和10.3的8.0 ,分别为(p?=?<?0.0001)。垂体SUVmax从10.2增加到11.0(p?=?0.004),而肾上腺和唾液腺SUVmax没有变化。 12例稳定疾病患者中有7例肿瘤SUVmax升高;这些患者中有5例CgA稳定或下降。 SSA治疗后30/49(61%)转移病灶的SUVmax升高,病灶-肝脏摄取率增加40/49(82%)。结论:长效SSA治疗可降低甲状腺的GaTate摄取,脾脏和肝脏,但在大多数情况下会增加转移灶内的摄取强度。这对治疗开始后解释GaTate PET / CT具有重要意义,因为单独增加强度可能并不代表真正的进展。我们的研究结果还表明,在PRRT之前预先服用SSA可以使更高剂量的药物递送至肿瘤,同时减少向正常组织的剂量。

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