Department of Radiology, LMU University Hospital, LMU Munich, Munich, Germany.
Interdisciplinary Center of Neuroendocrine Tumors of the GastroEnteroPancreatic System (GEPNET-KUM, ENETS certified Center of Excellence), LMU University Hospital, LMU Munich, Munich, Germany.
Eur Radiol. 2024 Nov;34(11):7222-7232. doi: 10.1007/s00330-024-10788-3. Epub 2024 May 20.
Somatostatin receptor positron emission tomography/computed tomography (SSTR-PET/CT) using [Ga]-labeled tracers is a widely used imaging modality for neuroendocrine tumors (NET). Recently, [F]SiTATE, a SiFAlin tagged [Tyr3]-octreotate (TATE) PET tracer, has shown great potential due to favorable clinical characteristics. We aimed to evaluate the reproducibility of Somatostatin Receptor-Reporting and Data System 1.0 (SSTR-RADS 1.0) for structured interpretation and treatment planning of NET using [F]SiTATE.
Four readers assessed [F]SiTATE-PET/CT of 95 patients according to the SSTR-RADS 1.0 criteria at two different time points. Each reader evaluated up to five target lesions per scan. The overall scan score and the decision on peptide receptor radionuclide therapy (PRRT) were considered. Inter- and intra-reader agreement was determined using the intraclass correlation coefficient (ICC).
The ICC analysis on the inter-reader agreement using SSTR-RADS 1.0 for identical target lesions (ICC ≥ 85%), overall scan score (ICC ≥ 90%), and the decision to recommend PRRT (ICC ≥ 85%) showed excellent agreement. However, significant differences were observed in recommending PRRT among experienced readers (ER) (p = 0.020) and inexperienced readers (IR) (p = 0.004). Compartment-based analysis demonstrated good to excellent inter-reader agreement for most organs (ICC ≥ 74%), except for lymph nodes (ICC ≥ 53%).
SSTR-RADS 1.0 represents a highly reproducible and consistent framework system for stratifying SSTR-targeted PET/CT scans, even using the novel SSTR-ligand [F]SiTATE. Some inter-reader variability was observed regarding the evaluation of uptake intensity prior to PRRT as well as compartment scoring of lymph nodes, indicating that those categories require special attention during further clinical validation and might be refined in a future SSTR-RADS version 1.1.
SSTR-RADS 1.0 is a consistent framework for categorizing somatostatin receptor-targeted PET/CT scans when using [F]SiTATE. The framework serves as a valuable tool for facilitating and improving the management of patients with NET.
SSTR-RADS 1.0 is a valuable tool for managing patients with NET. SSTR-RADS 1.0 categorizes patients with showing strong agreement across diverse reader expertise. As an alternative to [Ga]-labeled PET/CT in neuroendocrine tumor imaging, SSTR-RADS 1.0 reliably classifies [F]SiTATE-PET/CT.
使用 [Ga]-标记示踪剂的生长抑素受体正电子发射断层扫描/计算机断层扫描(SSTR-PET/CT)是神经内分泌肿瘤(NET)的一种广泛应用的成像方式。最近,[F]SiTATE,一种 SiFAlin 标记的 [Tyr3]-奥曲肽(TATE)PET 示踪剂,由于其良好的临床特征显示出巨大的潜力。我们旨在评估使用 [F]SiTATE 进行神经内分泌肿瘤的治疗计划时,Somatostatin Receptor-Reporting and Data System 1.0(SSTR-RADS 1.0)对结构性解释的可重复性。
四名读者根据 SSTR-RADS 1.0 标准在两个不同的时间点对 95 例患者的 [F]SiTATE-PET/CT 进行评估。每位读者评估每个扫描最多五个目标病变。考虑了总体扫描评分和肽受体放射性核素治疗(PRRT)的决定。使用组内相关系数(ICC)确定了读者间和读者内的一致性。
使用 SSTR-RADS 1.0 对相同的目标病变(ICC≥85%)、总体扫描评分(ICC≥90%)和推荐 PRRT 的决定进行的读者间 ICC 分析显示出极好的一致性。然而,在有经验的读者(ER)(p=0.020)和无经验的读者(IR)(p=0.004)之间,推荐 PRRT 存在显著差异。基于隔室的分析显示,大多数器官(ICC≥74%)的读者间一致性良好至极好,除了淋巴结(ICC≥53%)。
SSTR-RADS 1.0 代表了一种高度可重复和一致的框架系统,用于对 SSTR 靶向 PET/CT 扫描进行分层,即使使用新型 SSTR 配体 [F]SiTATE 也是如此。在 PRRT 之前评估摄取强度以及淋巴结隔室评分方面,观察到一些读者间的变异性,这表明在进一步的临床验证期间,这些类别需要特别注意,并且可能在未来的 SSTR-RADS 1.1 版本中进行细化。
SSTR-RADS 1.0 是使用 [F]SiTATE 对生长抑素受体靶向 PET/CT 扫描进行分类的一致框架。该框架是管理 NET 患者的有价值的工具。
SSTR-RADS 1.0 是管理 NET 患者的有价值的工具。SSTR-RADS 1.0 在不同的读者专业知识之间显示出强烈的一致性。作为神经内分泌肿瘤成像中 [Ga]-标记 PET/CT 的替代方法,SSTR-RADS 1.0 可可靠地对 [F]SiTATE-PET/CT 进行分类。