Lutetium-177 DOTATATE Production with an Automated Radiopharmaceutical Synthesis System

سال انتشار: 1394
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 450

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شناسه ملی سند علمی:

JR_JNMB-3-2_006

تاریخ نمایه سازی: 12 تیر 1398

چکیده مقاله:

Objective(s): Peptide Receptor Radionuclide Therapy (PRRT) with yttrium-90 (90Y) and lutetium-177 (177Lu)-labelled SST analogues are now therapy option for patients who have failed to respond to conventional medical therapy. In-house production with automated PRRT synthesis systems have clear advantages over manual methods resulting in increasing use in hospital-based radiopharmacies. We report on our one year experience with an automated radiopharmaceutical synthesis system.Methods: All syntheses were carried out using the Eckert & Ziegler Eurotope’s Modular-Lab Pharm Tracer® automated synthesis system. All materials and methods used were followed as instructed by the manufacturer of the system (Eckert & Ziegler Eurotope, Berlin, Germany). Sterile, GMP-certified, no-carrier added (NCA) 177Lu was used with GMPcertifiedpeptide. An audit trail was also produced and saved by the system. The quality of the final product was assessed after each synthesis by ITLCSG and HPLC methods.Results: A total of 17 [177Lu]-DOTATATE syntheses were performed between August 2013 and December 2014. The amount of radioactive [177Lu]-DOTATATE produced by each synthesis varied between 10-40 GBq and was dependant on the number of patients being treated on a given day. Thirteen individuals received a total of 37 individual treatment administrations in this period. There were no issues and failures with the system or the synthesis cassettes. The average radiochemical purity as determined by ITLC was above 99% (99.8 ± 0.05%) and the average radiochemical purity as determined by HPLC technique was above 97% (97.3 ± 1.5%) for this period.Conclusions: The automated synthesis of [177Lu]-DOTATATE using Eckert & Ziegler Eurotope’s Modular-Lab Pharm Tracer® system is a robust, convenient and high yield approach to the radiolabelling of DOTATATE peptide benefiting from the use of NCA 177Lu and almost negligible radiation exposure of the operators.

کلیدواژه ها:

Lutetium-DOTATATE ، Neuroendocrine Tumours ، automated synthesis ، Peptide Receptor Radionuclide Therapy

نویسندگان

Alireza Aslani

Department of Nuclear Medicine, Royal North Shore Hospital, Sydney, Australia

Graeme Snowdon

Department of Nuclear Medicine, Royal North Shore Hospital, Sydney, Australia

Dale Bailey

Faculty of Health Sciences, University of Sydney, Sydney, Australia

Geoffrey Schembri

Sydney Medical School, University of Sydney, Sydney, Australia

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