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64Cu Treatment Planning and 67Cu Therapy with Radiolabelled SARTATE ([64Cu/67Cu]MeCOSAR-Octreotate) in Subjects with Unresectable Multifocal Meningioma - Initial Results for Human Imaging, Safety, Biodistribution and Radiation Dosimetry.

医学 核医学 剂量学 生长抑素受体 体内分布 放射性核素治疗 不利影响 放射治疗 有效剂量(辐射) 放射科 生长抑素 内科学 体内 生物 生物技术
作者
Dale L. Bailey,Kathy Willowson,Matt Harris,Colin Biggin,Alireza Aslani,Nigel A Lengkeek,Jon Stoner,Enid M. Eslick,Harry Marquis,Michelle Parker,Paul J Roach,Geoffrey P Schembri
出处
期刊:The Journal of Nuclear Medicine [Society of Nuclear Medicine]
标识
DOI:10.2967/jnumed.122.264586
摘要

Aim: To report the use of copper-64 and copper-67 as a theranostic pair of radionuclides in human subjects. In addition, to measure whole organ dosimetry of copper-64 and copper-67 attached to the somatostatin analogue Octreotate using the sarcophagine MeCOSAR chelator ("SARTATE") in subjects with somatostatin receptor-expressing lesions confined to the cranium, thereby permitting normal organ dosimetry for the remainder of the body. Methods: Pre-treatment PET imaging studies were performed up to 24 hours after injection of [64Cu]Cu-SARTATE and normal organ dosimetry estimates were made using OLINDA/EXM. Subsequently the trial subjects with multifocal meningiomas were given therapeutic doses of [67Cu]Cu-SARTATE and imaged over a number of days using SPECT/CT. Results: Five subjects were initially recruited and imaged using PET/CT prior to treatment. Three of the subjects were subsequently administered four cycles each of [67Cu]Cu-SARTATE followed by multiple SPECT/CT imaging timepoints. No serious adverse events (SAEs) were observed and no adverse events led to withdrawal from the study or discontinuation from treatment. The mean Effective Dose estimated was 3.95 × 10-2 mSv/MBq for [64Cu]Cu-SARTATE and 7.62 × 10-2 mSv/MBq for [67Cu]Cu-SARTATE. The highest estimated organ dose was in spleen followed by kidneys, liver, adrenals and small intestine. The matched pairing was shown by PET and SPECT intra-subject imaging to have near identical targeting to tumours for guiding therapy, demonstrating a potentially accurate and precise theranostic product. Conclusion: Copper-64 and copper-67 show great promise as a theranostic pair of radionuclides. Further clinical studies will be required to examine the therapeutic dose required for [67Cu]Cu-SARTATE for various indications. In addition, the ability to use predictive copper-64 based dosimetry for treatment planning with copper-67 should be further explored.
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