Nuclear Medicine, Referral Cancer Center of Basilicata, 9267IRCCS CROB, Rionero in Vulture, Italy.
Cancer Control. 2023 Jan-Dec;30:10732748231152328. doi: 10.1177/10732748231152328.
We retrospectively aimed to assess the prognostic significance of somatostatin receptor (SSTR) standardized uptake value (SUVmax), SSTR representative tumor volume (RTV) and total lesion SSTR expression (TL) obtained by [Ga]Ga-edotreotide PET/CT ([Ga]Ga-SSTR PET/CT) in patients with primary gastroenteropancreatic neuroendocrine tumors (GEP-NET) before surgery.
We analyzed patients who underwent [Ga]Ga-SSTR PET/CT 3-6 weeks before surgery from February 2020 to April 2022. The mean SUVmax value, the RTV (cm3; 42% threshold) and the TL (g) were registered. Thereafter the patients were followed up 10.3 months (range 3-27). The PET/CT results were compared to the event free survival (EFS).
Forty-two patients (61 ± 13 years) have been enrolled. At multivariate analysis only RTV values were predictive. The Kaplan-Meier survival analysis for RTV showed a significant better EFS in patients presenting lower values as compared to those having greater ( = .003, log-rank test). SUVmax was not suitable for predicting EFS, TL mildly.
RTV represents a valuable volumetric parameter able to predict the outcome in GEP-NET patients who underwent surgery. The magnitude of the SSTR representative tumor burden holds a predominant value for determining the response to therapy in GEP-NET patients before surgery, rather than the maximal SSTR representation at single voxel.
我们回顾性评估了在手术前通过[Ga]Ga-奥曲肽 PET/CT([Ga]Ga-SSTR PET/CT)获得的生长抑素受体(SSTR)标准化摄取值(SUVmax)、SSTR 代表性肿瘤体积(RTV)和总病变 SSTR 表达(TL)对原发性胃肠胰神经内分泌肿瘤(GEP-NET)患者的预后意义。
我们分析了 2020 年 2 月至 2022 年 4 月期间手术前 3-6 周接受[Ga]Ga-SSTR PET/CT 的患者。登记了平均 SUVmax 值、RTV(cm3;42%阈值)和 TL(g)。此后,对患者进行了 10.3 个月(3-27 个月)的随访。将 PET/CT 结果与无事件生存(EFS)进行比较。
共纳入 42 名患者(61 ± 13 岁)。多变量分析仅 RTV 值具有预测性。RTV 的 Kaplan-Meier 生存分析显示,与 RTV 值较高的患者相比,RTV 值较低的患者 EFS 显著更好(=.003,对数秩检验)。SUVmax 不适合预测 EFS,TL 适度适合。
RTV 是一种有价值的体积参数,能够预测接受手术的 GEP-NET 患者的预后。在手术前的 GEP-NET 患者中,SSTR 代表性肿瘤负担的大小对于确定对治疗的反应具有主要价值,而不是单个体素的最大 SSTR 表现。