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Radiation dosimetry, pharmacokinetics and safety evaluation of 177Lu-DOTA-TATE in the treatment of advanced metastatic neuroendocrine tumors

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Author:
No author available
Journal Title:
International Journal of Radiation Medicine and Nuclear Medicine
Issue:
12
DOI:
10.3760/cma.j.cn121381-202303028-00370
Key Word:
镥;奥曲肽;神经内分泌瘤;辐射剂量;受体,生长抑素;药物代谢动力学;Lutetium;Octreotide;Neuroendocrine tumors;Radiation dosage;Receptors, somatostatin;Pharmacokinetics

Abstract: Objective:To evaluate the radiation dosimetry, pharmacokinetics, and safety of 177Lu-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-D-Phe1-Tyr3-Thr8-octreotate ( 177Lu-DOTA-TATE) in the treatment of advanced metastatic neuroendocrine tumors (NETs). Methods:A prospective analysis was performed for 6 patients with advanced metastatic NETs diagnosed by histopathological examination in the First Medical Center of PLA General Hospital from July 2021 to March 2022, including 4 males and 2 females, aged (50.2±9.6) years old. Patients were given intravenous injection of 177Lu-DOTA-TATE at a single dose of (7 400±740) MBq for up to 4 cycles, with each cycle interval of (8±1) weeks. Considering the difficulties in the supply of 177LuCl 3 raw materials owing to pandemic, only 3 patients received a full 4 cycles of treatment, 1 patient received 3 cycles treatment and 2 patients received 1 cycles treatment and then withdrew from the study. The distribution and metabolism of 177Lu-DOTA-TATE in patients were analyzed, and the related parameters such as radiation dosimetry and pharmacokinetics were calculated, safety follow-up was also carried out. Patients undergoing radiation dosimetry and pharmacokinetic studies were subjected to SPECT images, blood samples, and urine samples at different time points after the first dose. Paired-sample t-test was used to compare the measured data with normal distribution and homogeneity of variance. Results:The dosimetry study of 177Lu-DOTA-TATE was completed in 3 patients with NETs. The absorbed dose of 177Lu-DOTA-TATE decreased in the following order: focus > kidney > spleen > liver. Three patients completed the pharmacokinetics study at the same time; the average calculated peak concentration (C max) was 16.61 μg/L, and the average concentration time AUC (AUC 0-t) from zero to the last quantifiable concentration was 57.11 μg/(L·h). The average value of AUC (AUC 0-∞) extrapolated from zero to infinity was 76.25 μg/(L·h), the average apparent volume of distribution (V z) was 222.55 L, the average clearance rate (CL) was 3.44 L/h, and the average half-life (T 1/2α) of the distributed phase was 0.89 h. The mean half-life (T 1/2β) of the elimination phase was 48.94 h. 177Lu-DOTA-TATE was metabolized primarily by the kidney. The cumulative excretion rate of 177Lu-DOTA-TATE was 61.05% within 48 h after administration. No serious adverse events occurred during the safety follow-up period after 177Lu-DOTA-TATE therapy in 6 patients. No significant difference in blood routine, blood biochemistry, coagulation function and urine routine was found before and after treatment ( t=-1.437 to 1.378, all P>0.05). Conclusions:177Lu-DOTA-TATE is excreted mostly in the urinary system, with rapid clearance in vivo and high tumor uptake. It has good safety and tolerance in patients with advanced metastatic neuroendocrine tumors.

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