Service de Médecine Nucléaire, CHU de Bordeaux, LabEx TRAIL, Université de Bordeaux, France.
Theranostics. 2017 Mar 1;7(5):1159-1163. doi: 10.7150/thno.19588. eCollection 2017.
Neuroendocrine tumors (NET) are often metastatic at the time of diagnosis. Metastatic well-differentiated (G1/G2) NET may display a wide range of behaviors, ranging from indolent to aggressive, even within apparently homogeneous categories. Thus, selecting the optimal treatment strategy is a challenging task. Somatostatin receptor imaging (SRI) is the standard molecular imaging technique for well-differentiated NET. When performed with Ga-labeled somatostatin analogs (SRI-PET), it offers exquisite sensitivity for disease staging. SRI is also a prerequisite for using targeted radionuclide therapy (e.g. Lu-DOTATATE). 18F-FDG imaging has traditionally been reserved for staging poorly-differentiated G3 neuroendocrine carcinomas. However, recent data showed that FDG imaging has prognostic value in patients with well-differentiated NET: high uptake was associated with an increased risk of early progression while low uptake suggested an indolent tumor. In this issue of the Journal, Chan and colleagues propose a grading system where the results from the combined reading of SRI-PET and FDG-PET are reported as a single parameter, the "NETPET" score. While the scoring system still needs validation, it is clear that time has come to think about FDG and SRI in metastatic NET not as competitors but as complementary imaging modalities. Dual-tracer imaging can be viewed as a way to characterize disease phenotype in the whole-body. Moving from the prognostic value of dual-tracer imaging to a tool that allows for individualized management would require prospective trials. This editorial will argue that dual-tracer FDG-PET and SRI-PET might influence management of patients with well-differentiated metastatic NET and help selecting between different therapy options.
神经内分泌肿瘤(NET)在诊断时常常已经发生转移。转移性高分化(G1/G2)NET 可能表现出广泛的行为,从惰性到侵袭性,即使在明显同质的类别中也是如此。因此,选择最佳的治疗策略是一项具有挑战性的任务。生长抑素受体成像(SRI)是分化良好的 NET 的标准分子成像技术。当与 Ga 标记的生长抑素类似物(SRI-PET)一起使用时,它为疾病分期提供了极高的灵敏度。SRI 也是使用靶向放射性核素治疗(例如 Lu-DOTATATE)的前提。18F-FDG 成像传统上仅用于分期低分化 G3 神经内分泌癌。然而,最近的数据表明,FDG 成像在分化良好的 NET 患者中具有预后价值:高摄取与早期进展的风险增加相关,而低摄取则提示肿瘤惰性。在本期杂志中,Chan 及其同事提出了一种分级系统,其中 SRI-PET 和 FDG-PET 联合阅读的结果被报告为一个单一参数,即“NETPET”评分。虽然评分系统仍需要验证,但很明显,现在是时候将 FDG 和 SRI 视为转移性 NET 的互补成像方式,而不是竞争对手了。双示踪剂成像可以被视为一种在全身范围内对疾病表型进行特征描述的方法。从双示踪剂成像的预后价值转变为一种允许个体化管理的工具,需要进行前瞻性试验。本社论将认为,双示踪剂 FDG-PET 和 SRI-PET 可能会影响高分化转移性 NET 患者的管理,并有助于选择不同的治疗方案。