Bombardieri E, Seregni E, Villano C, Chiti A, Bajetta E
Nuclear Medicine Division, Istituto Nazionale Tumori, Milan, Italy.
Q J Nucl Med Mol Imaging. 2004 Jun;48(2):150-63.
In recent years nuclear medicine has contributed to the impressive development of the knowledge of neuroendocrine tumors in terms of biology (receptor scintigraphy), pharmacology (development of new tracers), and therapy (radiometabolic therapy). At present, it is impossible to plan the management of a patient affected by a neuroendocrine tumor without performing nuclear medicine examinations. The contribution of nuclear medicine had affected and improved the management of these patients by offering various important options that are part of the modern diagnosis and treatment protocols. The clinical experience and the literature confirm that, among the wide variety of tracers and nuclear medicine modalities available today, metaiodobenzylguanidine (MIBG) and DTPA-D-Phe-octreotide (pentetreotide) are the radiopharmaceuticals of current clinical use. Several new somatostatin analogues are under investigation. Positron emission tomography (PET) supplies a range of labelled compounds to be used for the visualization of tumor biochemistry. In addition to the first routinely used PET tracer in oncology, 18F-labelled deoxyglucose (FDG), a number of radiopharmaceuticals based on different precursors such as fluorodopamine and 5-hydroxytryptophan (5-HTP) are going to gain a clinical role. Of course, the diagnosis of neuroendocrine tumors has to be based on integrated information derived from different examinations including nuclear medicine studies. The clinical presentation of neuroendocrine tumors is highly variable: sometimes they manifest typical or atypical symptoms but they may also be detected by chance during an X-ray or ultrasound examination carried out for other reasons. At disease presentation nuclear medicine modalities are sometimes able to direct physicians towards the clinical diagnosis thanks to the specificity of their imaging mechanisms. They also play a role in disease staging and restaging, patient follow-up and treatment monitoring. In addition, the biological characterisation of neuroendocrine tissues (receptor status, glucose metabolism, differentiation, etc.) allows the interpretation of radiopharmaceutical uptake as a prognostic parameter and sometimes as a predictor of the response to treatment.
近年来,核医学在神经内分泌肿瘤的生物学(受体闪烁显像)、药理学(新型示踪剂的研发)和治疗(放射性代谢治疗)等方面,推动了该领域知识的显著发展。目前,若不进行核医学检查,就无法规划神经内分泌肿瘤患者的治疗方案。核医学通过提供现代诊断和治疗方案中的各种重要选择,影响并改善了这些患者的治疗。临床经验和文献证实,在当今可用的多种示踪剂和核医学检查方法中,间碘苄胍(MIBG)和二巯基丁二酸 - D - 苯丙氨酸 - 奥曲肽(喷替肽)是目前临床使用的放射性药物。几种新型生长抑素类似物正在研究中。正电子发射断层扫描(PET)提供了一系列用于肿瘤生物化学可视化的标记化合物。除了肿瘤学中首个常规使用的PET示踪剂18F - 脱氧葡萄糖(FDG)外,一些基于不同前体(如氟多巴胺和5 - 羟色氨酸(5 - HTP))的放射性药物也将发挥临床作用。当然,神经内分泌肿瘤的诊断必须基于包括核医学研究在内的不同检查所获得的综合信息。神经内分泌肿瘤的临床表现高度多样:有时它们表现出典型或非典型症状,但也可能在因其他原因进行的X线或超声检查中偶然被发现。在疾病初发时,由于其成像机制的特异性,核医学检查方法有时能够引导医生做出临床诊断。它们在疾病分期和再分期、患者随访及治疗监测中也发挥着作用。此外,神经内分泌组织的生物学特性(受体状态、葡萄糖代谢、分化等)有助于将放射性药物摄取解释为预后参数,有时还可作为治疗反应的预测指标。