University Medical Imaging Toronto; University Health Network, Sinai Health Systems, Women's College Hospital; and University of Toronto, Toronto, Ontario, Canada;
Division of Medical Oncology, University of Toronto; and Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
J Nucl Med. 2024 Oct 1;65(10):1591-1596. doi: 10.2967/jnumed.124.267982.
Our purpose was to prospectively assess the distribution of NETPET scores in well-differentiated (WD) grade 2 and 3 gastroenteropancreatic (GEP) neuroendocrine tumors (NETs) and to determine the impact of the NETPET score on clinical management. This single-arm, institutional ethics review board-approved prospective study included 40 patients with histologically proven WD GEP NETs. Ga-DOTATATE PET and F-FDG PET were performed within 21 d of each other. NETPET scores were evaluated qualitatively by 2 reviewers, with up to 10 marker lesions selected for each patient. The quantitative parameters that were evaluated included marker lesion SUV for each tracer; F-FDG/Ga-DOTATATE SUV ratios; functional tumor volume (FTV) and metabolic tumor volume (MTV) on Ga-DOTATATE and F-FDG PET, respectively; and FTV/MTV ratios. The treatment plan before and after F-FDG PET was recorded. There were 22 men and 18 women (mean age, 60.8 y) with grade 2 ( = 24) or grade 3 ( = 16) tumors and a mean Ki-67 index of 16.1%. NETPET scores of P0, P1, P2A, P2B, P3B, P4B, and P5 were documented in 2 (5%), 5 (12.5%), 5 (12.5%) 20 (50%), 2 (5%), 4 (10%), and 2 (5%) patients, respectively. No association was found between the SUV of target lesions on Ga-DOTATATE and the SUV of target lesions on F-FDG PET ( = 0.505). F-FDG/Ga-DOTATATE SUV ratios were significantly lower for patients with low (P1-P2) primary NETPET scores than for those with high (P3-P5) primary NETPET scores (mean ± SD, 0.20 ± 0.13 and 1.68 ± 1.44, respectively; < 0.001). MTV on F-FDG PET was significantly lower for low primary NETPET scores than for high ones (mean ± SD, 464 ± 601 cm and 66 ± 114 cm, respectively; = 0.005). A change in the type of management was observed in 42.5% of patients after F-FDG PET, with the most common being a change from systemic therapy to peptide receptor radionuclide therapy and from debulking surgery to systemic therapy. There was a heterogeneous distribution of NETPET scores in patients with WD grade 2 and 3 GEP NETs, with more than 1 in 5 patients having a high NETPET score and a frequent change in management after F-FDG PET. Quantitative parameters including F-FDG/Ga-DOTATATE SUV ratios in target lesions and FTV/MTV ratios can discriminate between patients with high and low NETPET scores.
我们的目的是前瞻性评估分化良好(WD)2 级和 3 级胃肠胰神经内分泌肿瘤(NET)的 NETPET 评分分布,并确定 NETPET 评分对临床管理的影响。这项单臂、机构伦理审查委员会批准的前瞻性研究纳入了 40 名经组织学证实的 WD GEP NET 患者。在彼此 21 天内进行 Ga-DOTATATE PET 和 F-FDG PET。NETPET 评分由 2 名评审员进行定性评估,每位患者最多选择 10 个标记病变。评估的定量参数包括每个示踪剂的标记病变 SUV;F-FDG/Ga-DOTATATE SUV 比值;Ga-DOTATATE 和 F-FDG PET 上的功能性肿瘤体积(FTV)和代谢肿瘤体积(MTV),以及 FTV/MTV 比值。记录 F-FDG PET 前后的治疗计划。22 名男性和 18 名女性(平均年龄 60.8 岁),肿瘤分级 2 级( = 24)或 3 级( = 16),平均 Ki-67 指数为 16.1%。P0、P1、P2A、P2B、P3B、P4B 和 P5 的 NETPET 评分分别记录在 2(5%)、5(12.5%)、5(12.5%)、20(50%)、2(5%)、4(10%)和 2(5%)名患者中。Ga-DOTATATE 上靶病变的 SUV 与 F-FDG PET 上靶病变的 SUV 之间未见相关性( = 0.505)。低(P1-P2)原发 NETPET 评分患者的 F-FDG/Ga-DOTATATE SUV 比值明显低于高(P3-P5)原发 NETPET 评分患者(均值 ± 标准差,0.20 ± 0.13 和 1.68 ± 1.44,分别; <0.001)。低原发 NETPET 评分患者的 F-FDG PET 上 MTV 明显低于高原发 NETPET 评分患者(均值 ± 标准差,464 ± 601 cm 和 66 ± 114 cm,分别; = 0.005)。42.5%的患者在 F-FDG PET 后管理方式发生变化,最常见的是从全身治疗改为肽受体放射性核素治疗,从肿瘤切除术改为全身治疗。WD 2 级和 3 级 GEP NET 患者的 NETPET 评分分布不均,超过 1/5 的患者 NETPET 评分较高,且 F-FDG PET 后管理方式经常发生变化。定量参数包括靶病变中 F-FDG/Ga-DOTATATE SUV 比值和 FTV/MTV 比值可区分高 NETPET 评分和低 NETPET 评分患者。