Nuclear Medicine Unit, Department of Medical Sciences, University of Turin, Turin, Italy;
Department of Endocrinology, University Hospital of Brest, Brest, France.
J Nucl Med. 2022 Jul;63(7):1014-1020. doi: 10.2967/jnumed.121.262652. Epub 2021 Nov 5.
Our objective was to evaluate the prognostic value of somatostatin receptor tumor burden on Ga-DOTATOC PET/CT in patients with well-differentiated (WD) neuroendocrine tumors (NETs). We retrospectively analyzed the Ga-DOTATOC PET/CT scans of 84 patients with histologically confirmed WD NETs (51 grade 1, 30 grade 2, and 3 grade 3). For each PET/CT scan, all Ga-DOTATOC-avid lesions were independently segmented by 2 operators using a customized threshold based on the healthy liver SUV (LIFEx, version 5.1). Somatostatin receptor-expressing tumor volume (SRETV) and total lesion somatostatin receptor expression (TLSRE = SRETV × SUV) were extracted for each lesion, and then whole-body SRETV and TLSRE (SRETVwb and TLSREwb, respectively) were defined as the sum of SRETV and TLSRE, respectively, for all segmented lesions in each patient. Time to progression (TTP) was defined as the combination of disease-free survival in patients undergoing curative surgery ( = 10) and progression-free survival for patients with unresectable or metastatic disease ( = 74). TTP and overall survival were calculated by Kaplan-Meier analysis, log-rank testing, and the Cox proportional-hazards regression model. After a median follow-up of 15.5 mo, disease progression was confirmed in 35 patients (41.7%) and 14 patients died. A higher SRETVwb (>39.1 cm) and TLSREwb (>306.8 g) correlated significantly with a shorter median TTP (12 mo vs. not reached; < 0.001). In multivariate analysis, SRETVwb ( = 0.005) was the only independent predictor of TTP regardless of histopathologic grade and TNM staging. According to our results, SRETVwb and TLSREwb extracted from Ga-DOTATOC PET/CT could predict TTP or overall survival and might have important clinical utility in the management of patients with WD NETs.
我们的目的是评估生长抑素受体肿瘤负荷在 Ga-DOTATOC PET/CT 对分化良好(WD)神经内分泌肿瘤(NETs)患者的预后价值。我们回顾性分析了 84 例经组织学证实的 WD NETs 患者的 Ga-DOTATOC PET/CT 扫描结果(51 级 1 例,30 级 2 例,3 级 3 例)。对于每一次 PET/CT 扫描,两位操作人员使用基于健康肝脏 SUV 的定制阈值(LIFEx,版本 5.1)独立分割所有 Ga-DOTATOC 阳性病灶。提取每个病灶的生长抑素受体表达肿瘤体积(SRETV)和总病变生长抑素受体表达(TLSRE=SRETV×SUV),然后定义全身 SRETV 和 TLSRE(SRETVwb 和 TLSREwb)分别为每位患者所有分割病灶的 SRETV 和 TLSRE 的总和。无进展生存期(TTP)定义为接受根治性手术的患者的无病生存期(=10)和不可切除或转移性疾病患者的无进展生存期(=74)的组合。TTP 和总生存期通过 Kaplan-Meier 分析、对数秩检验和 Cox 比例风险回归模型进行计算。中位随访 15.5 个月后,35 例(41.7%)患者疾病进展得到证实,14 例患者死亡。更高的 SRETVwb(>39.1 cm)和 TLSREwb(>306.8 g)与较短的中位 TTP(12 个月与未达到;<0.001)显著相关。多变量分析显示,SRETVwb(=0.005)是 TTP 的唯一独立预测因素,与组织病理学分级和 TNM 分期无关。根据我们的结果,从 Ga-DOTATOC PET/CT 提取的 SRETVwb 和 TLSREwb 可以预测 TTP 或总生存期,并且可能对 WD NETs 患者的管理具有重要的临床应用价值。