Department of Nuclear Medicine, Erasmus Medical Center, s-Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands.
Endocr Relat Cancer. 2010 Jan 29;17(1):R53-73. doi: 10.1677/ERC-09-0078. Print 2010 Mar.
Somatostatin receptor imaging (SRI) with [(111)In-DTPA(0)]octreotide has proven its role in the diagnosis and staging of gastroenteropancreatic neuroendocrine tumors (GEPNETs). Newer radiolabeled somatostatin analogs which can be used in positron emission tomography (PET) imaging, and which have a higher affinity for the somatostatin receptor, especially receptor subtype-2, have been developed. It would be desirable, however, if one radiolabeled analog became the new standard for PET imaging, because the current application of a multitude of analogs implies a fragmented knowledge on the interpretation of the images that are obtained in clinical practice. In our view, the most likely candidates for such a universal PET tracer for SRI are [(68)Ga-DOTA(0),Tyr(3)]octreotate or [(68)Ga-DOTA(0),Tyr(3)]octreotide. Treatment with radiolabeled somatostatin analogs is a promising new tool in the management of patients with inoperable or metastasized neuroendocrine tumors. Symptomatic improvement may occur with all (111)In-, (90)Y-, or (177)Lu-labeled somatostatin analogs that have been used for peptide receptor radionuclide therapy (PRRT). The results that were obtained with [(90)Y-DOTA(0),Tyr(3)]octreotide and [(177)Lu-DOTA(0),Tyr(3)]octreotate are very encouraging in terms of tumor regression. Also, if kidney protective agents are used, the side effects of this therapy are few and mild, and the median duration of the therapy response for these radiopharmaceuticals is 30 and 40 months respectively. The patients' self-assessed quality of life increases significantly after treatment with [(177)Lu-DOTA(0),Tyr(3)]octreotate. Lastly, compared to historical controls, there is a benefit in overall survival of several years from the time of diagnosis in patients treated with [(177)Lu-DOTA(0),Tyr(3)]octreotate. These data compare favorably with the limited number of alternative treatment approaches. If more widespread use of PRRT can be guaranteed, such therapy may well become the therapy of first choice in patients with metastasized or inoperable GEPNETs.
生长抑素受体成像(SRI)结合 [(111)In-DTPA(0)]奥曲肽已被证明可用于诊断和分期胃肠胰神经内分泌肿瘤(GEPNETs)。已经开发出了新型放射性标记的生长抑素类似物,可用于正电子发射断层扫描(PET)成像,并且对生长抑素受体,特别是受体亚型-2 具有更高的亲和力。然而,如果有一种放射性标记的类似物成为 PET 成像的新标准,这将是理想的,因为目前大量类似物的应用意味着在解释在临床实践中获得的图像时,知识是碎片化的。在我们看来,用于 SRI 的这种通用 PET 示踪剂最有可能的候选物是 [(68)Ga-DOTA(0),Tyr(3)]奥曲肽或 [(68)Ga-DOTA(0),Tyr(3)]奥曲肽。用放射性标记的生长抑素类似物治疗是治疗不可切除或转移性神经内分泌肿瘤患者的一种有前途的新工具。使用所有用于肽受体放射性核素治疗(PRRT)的 [(111)In-、(90)Y- 或 (177)Lu-] 标记生长抑素类似物都可能出现症状改善。[(90)Y-DOTA(0),Tyr(3)]奥曲肽和 [(177)Lu-DOTA(0),Tyr(3)]奥曲肽的结果在肿瘤消退方面非常令人鼓舞。此外,如果使用肾脏保护剂,该治疗的副作用很少且温和,并且这些放射性药物的治疗反应中位数持续时间分别为 30 个月和 40 个月。治疗后,患者的自我评估生活质量显着提高 [(177)Lu-DOTA(0),Tyr(3)]奥曲肽。最后,与历史对照相比,在接受 [(177)Lu-DOTA(0),Tyr(3)]奥曲肽治疗的患者中,从诊断开始的总生存期延长了数年。这些数据与有限数量的替代治疗方法相比具有优势。如果可以保证 PRRT 的更广泛使用,那么这种治疗方法很可能成为转移性或不可切除的 GEPNETs 患者的首选治疗方法。