From the Neuroendocrine Tumour Unit, ENETS Centre of Excellence, Royal Free Hospital.
Medical School, University College London.
Clin Nucl Med. 2022 Jan 1;47(1):26-35. doi: 10.1097/RLU.0000000000003937.
Gastroenteropancreatic neuroendocrine neoplasms (GEP NEN) are widely heterogeneous in their biological behavior, and predicting prognosis and optimal treatment strategies can be challenging. 68Ga-DOTATATE PET/CT is a sensitive imaging modality for well-differentiated NEN and indicates a favorable prognosis, whereas 18F-FDG PET/CT avidity indicates disease that is potentially more aggressive. There has been emerging interest in the combined interpretation of 68Ga-DOTATATE and 18F-FDG PET and its prognostic significance. We aimed to assess the prognostic utility of a classification system that incorporates the complex findings of 68Ga-DOTATATE and 18F-FDG PET interpreted side-by-side in patients with metastatic GEP NEN.
We defined 3 68Ga-DOTATATE/18F-FDG "dual-tracer PET" groups: D1 (68Ga-DOTATATE positive/18F-FDG negative), D2 (68Ga-DOTATATE positive/18F-FDG positive), and D3 (68Ga-DOTATATE negative/18F-FDG positive). We retrospectively assessed the association between the dual-tracer PET classification and progression-free and overall survival (OS) using Kaplan-Meier analysis. Univariate and multivariate analyses were performed using the Cox proportional hazards model.
Eighty-seven patients with metastatic GEP NEN and contemporaneous 68Ga-DOTATATE and 18F-FDG PET were included. The dual-tracer PET classification was an independent predictor of OS (multivariate P = 0.016) and also predicted progression-free survival (univariate P = 0.030). Other independent predictors of OS included chromogranin A and World Health Organization (WHO) grade. WHO grade was not associated with OS from the time of dual-tracer PET but was an independent predictor of OS from the date of histological diagnosis (multivariate P = 0.003).
Our study demonstrates that a classification system combining the complex findings of 68Ga-DOTATATE and 18F-FDG PET is correlated with prognosis. Further research is needed to prospectively validate these findings and to explore whether dual-tracer PET scores may also be able to predict response to treatment.
胃肠胰神经内分泌肿瘤(GEP NEN)在生物学行为上具有广泛的异质性,因此预测预后和最佳治疗策略具有挑战性。68Ga-DOTATATE PET/CT 是一种用于分化良好的 NEN 的敏感成像方式,提示预后良好,而 18F-FDG PET/CT 的摄取则表明疾病可能更具侵袭性。人们对同时解读 68Ga-DOTATATE 和 18F-FDG PET 及其预后意义的兴趣日益浓厚。我们旨在评估一种分类系统的预后实用性,该系统结合了转移性 GEP NEN 患者并排解读的 68Ga-DOTATATE 和 18F-FDG PET 的复杂发现。
我们定义了 3 个 68Ga-DOTATATE/18F-FDG“双示踪剂 PET”组:D1(68Ga-DOTATATE 阳性/18F-FDG 阴性)、D2(68Ga-DOTATATE 阳性/18F-FDG 阳性)和 D3(68Ga-DOTATATE 阴性/18F-FDG 阳性)。我们使用 Kaplan-Meier 分析回顾性评估双示踪剂 PET 分类与无进展生存期和总生存期(OS)之间的关联。使用 Cox 比例风险模型进行单变量和多变量分析。
共纳入 87 例转移性 GEP NEN 患者和同期 68Ga-DOTATATE 和 18F-FDG PET。双示踪剂 PET 分类是 OS 的独立预测因子(多变量 P=0.016),也预测了无进展生存期(单变量 P=0.030)。OS 的其他独立预测因子包括嗜铬粒蛋白 A 和世界卫生组织(WHO)分级。WHO 分级与双示踪剂 PET 时的 OS 无关,但与组织学诊断时的 OS 相关(多变量 P=0.003)。
我们的研究表明,一种结合 68Ga-DOTATATE 和 18F-FDG PET 复杂发现的分类系统与预后相关。需要进一步的前瞻性研究来验证这些发现,并探讨双示踪剂 PET 评分是否也能够预测治疗反应。