Department of Oncology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
J Nucl Med. 2011 Jul;52(7):1041-7. doi: 10.2967/jnumed.110.085100. Epub 2011 Jun 16.
This study tested the principle that (68)Ga-DOTATATE PET/CT may be used to select children with primary refractory or relapsed high-risk neuroblastoma for treatment with (177)Lu-DOTATATE and evaluated whether this is a viable therapeutic option for those children.
Between 2008 and 2010, 8 children with relapsed or refractory high-risk neuroblastoma were studied with (68)Ga-DOTATATE PET/CT. The criterion of eligibility for (177)Lu-DOTATATE therapy was uptake on the diagnostic scan equal to or higher than that of the liver.
Of the 8 children imaged, 6 had abnormally high uptake on the (68)Ga-DOTATATE PET/CT scan and proceeded to treatment. Patients received 2 or 3 administrations of (177)Lu-DOTATATE at a median interval of 9 wk and a median administered activity of 7.3 GBq. Of the 6 children treated, 5 had stable disease by the response evaluation criteria in solid tumors (RECIST). Of these 5 children, 2 had an initial metabolic response and reduction in the size of their lesions, and 1 patient had a persistent partial metabolic response and reduction in size of the lesions on CT, although the disease was stable by RECIST. One had progressive disease. Three children had grade 3 and 1 child had grade 4 thrombocytopenia. No significant renal toxicity has been seen.
(68)Ga-DOTATATE can be used to image children with neuroblastoma and identify those suitable for molecular radiotherapy with (177)Lu-DOTATATE. We have shown, for what is to our knowledge the first time, that treatment with (177)Lu-DOTATATE is safe and feasible in children with relapsed or primary refractory high-risk neuroblastoma. We plan to evaluate this approach formally in a phase I-II clinical trial.
本研究旨在验证(68)Ga-DOTATATE PET/CT 可用于选择原发性难治性或复发性高危神经母细胞瘤患儿接受(177)Lu-DOTATATE 治疗的原理,并评估该方法是否适用于此类患儿。
2008 年至 2010 年,8 例复发性或难治性高危神经母细胞瘤患儿接受(68)Ga-DOTATATE PET/CT 检查。(177)Lu-DOTATATE 治疗的入选标准为诊断性扫描摄取与肝脏摄取相等或更高。
8 例患儿中,6 例(68)Ga-DOTATATE PET/CT 扫描摄取异常增高,接受治疗。患者每 9 周接受 2 或 3 次(177)Lu-DOTATATE 治疗,中位给药活度为 7.3GBq。6 例接受治疗的患儿中,根据实体瘤反应评价标准(RECIST),5 例疾病稳定。这 5 例患儿中,2 例初始代谢应答且肿瘤缩小,1 例持续部分代谢应答且 CT 显示肿瘤缩小,尽管 RECIST 显示疾病稳定。1 例疾病进展。3 例患儿出现 3 级血小板减少,1 例患儿出现 4 级血小板减少。未见明显肾毒性。
(68)Ga-DOTATATE 可用于成像神经母细胞瘤患儿,并识别适合接受(177)Lu-DOTATATE 分子放疗的患儿。我们首次表明,(177)Lu-DOTATATE 治疗复发性或原发性难治性高危神经母细胞瘤患儿是安全可行的。我们计划在 I/II 期临床试验中对此方法进行正式评估。