1. Nuclear medicine & PET, Uppsala University and Medical Sciences, Uppsala University Hospital, Uppsala, Sweden;
Theranostics. 2012;2(5):459-71. doi: 10.7150/thno.3594. Epub 2012 May 9.
Favourable outcomes of peptide receptor radiotherapy (PRRT) of neuroendocrine tumours have been reported during the last years. Still, there are uncertainties on the radionuclides to be used, the treatment planning, and the indication in patients with a high proliferation rate.This case report describes a patient with a high tumour burden of poorly differentiated neuroendocrine carcinoma of unknown primary with a proliferation rate in liver metastases up to 50%, undergoing fractionated treatment with 7 cycles of (177)Lu-DOTA-octreotate (7.4 GBq each) after disease progression on two different chemotherapy regiments. Based on initial staging scintigraphy, somatostatin receptor expression was very high.Longitudinal dosimetry studies during therapy indicated ongoing increases in tumour-to-organ ratios that coincided with an objective response.We conclude that fractionated therapy with (177)Lu-DOTA-octreotate should be considered a treatment option also for those patients with large tumours, high proliferation, and high receptor expression.
近年来,已有研究报道肽受体放射性核素疗法(PRRT)治疗神经内分泌肿瘤的疗效良好。但对于使用何种放射性核素、如何制定治疗计划以及高增殖率患者的适应证仍存在不确定性。本病例报告描述了一例高肿瘤负荷、分化差的不明原发部位神经内分泌癌患者,其肝转移灶的增殖率高达 50%,在两种不同化疗方案治疗进展后,接受了 7 个周期的(177)Lu-DOTA-奥曲肽(每次 7.4GBq)分段治疗。基于初始分期闪烁扫描,生长抑素受体表达非常高。治疗过程中的纵向剂量学研究表明,肿瘤与器官比值持续增加,与客观缓解一致。我们得出结论,(177)Lu-DOTA-奥曲肽分段治疗也应考虑作为那些肿瘤较大、增殖率高、受体表达高的患者的治疗选择。