Department of Advanced Biomedical Sciences, University of Naples, Federico II, 80131 Naples, Italy.
Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy.
Curr Oncol. 2024 Sep 18;31(9):5617-5629. doi: 10.3390/curroncol31090416.
The aim of the present study was to evaluate the safety and efficacy of radionuclide therapy with [Lu]Lu-DOTA-TATE according to our single center experience at the University of Naples Federico II. For the present analysis, we considered 21 patients with progressive, advanced, well-differentiated G1 and G2 in patients with gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs) treated with [Lu]Lu-DOTA-TATE according to the decisions of a multidisciplinary team. All patients underwent four cycles of 7-8 GBq of [Lu]Lu-DOTA-TATE every 8 weeks. A whole-body scan (WBS) was performed 4, 48, and 168 h after each treatment. The dosimetry towards the organ at risk and target lesions was calculated. For each patient, renal and bone marrow parameters were evaluated before, during, and 3 months after the end of the treatment. Follow-up data were obtained and RECIST criteria were considered as the endpoint. Among 21 patients enrolled (mean age 65 ± 9 years); 17 (81%) were men and the small intestine was the most frequent location of disease (n = 12). A mild albeit significant variation ( < 0.05) in both platelets and white blood cell counts among all time points was observed, despite it disappearing 3 months after the end of the therapy. According to the RECIST criteria, 11 (55%) patients had a partial response to therapy and 8 (40%) had stable disease. Only one (5%) patient had disease progression 4 months after treatment. Our data confirm that [Lu]Lu-DOTA is safe and effective in controlling the burden disease of G1/G2 GEP-NETs patients.
本研究旨在评估我们在那不勒斯费德里克二世大学的单中心经验中,使用 [Lu]Lu-DOTA-TATE 进行放射性核素治疗的安全性和疗效。在本分析中,我们考虑了 21 名患有进展性、晚期、高分化 G1 和 G2 的胃-肠-胰腺(GEP)神经内分泌肿瘤(NETs)的患者,他们根据多学科团队的决定接受了 [Lu]Lu-DOTA-TATE 治疗。所有患者每 8 周接受 7-8GBq 的 [Lu]Lu-DOTA-TATE 四个周期。每次治疗后 4、48 和 168 小时进行全身扫描(WBS)。计算了对风险器官和靶病变的剂量学。对于每位患者,在治疗前、治疗中和治疗结束后 3 个月评估了肾和骨髓参数。获得随访数据并将 RECIST 标准视为终点。在入组的 21 名患者中(平均年龄 65 ± 9 岁);17 名(81%)为男性,小肠是最常见的疾病部位(n = 12)。尽管在治疗结束后 3 个月消失,但在所有时间点均观察到血小板和白细胞计数的轻度但显著变化(<0.05)。根据 RECIST 标准,11 名(55%)患者对治疗有部分反应,8 名(40%)患者病情稳定。只有一名(5%)患者在治疗后 4 个月出现疾病进展。我们的数据证实 [Lu]Lu-DOTA 安全有效,可控制 G1/G2 GEP-NETs 患者的疾病负担。