Literature DB >> 29189490

Excretion and whole-body retention of radium-223 dichloride administered for the treatment of bone metastases from castration resistant prostate cancer.

Brenda E Pratt1, Cecilia Hindorf1, Sarah J Chittenden1, Christopher C Parker2, Glenn D Flux1.   

Abstract

OBJECTIVE: The aim of the study was to determine the fraction of administered activity that was excreted and retained by a small cohort of patients who each received treatment with radium-223 dichloride (Ra). Ra is an α-emitting radionuclide that has been approved for use in the treatment of bone metastases that are secondary to castration resistant prostate cancer. PATIENTS AND METHODS: Six patients received two weight-based administrations of Ra 6 weeks apart. Activity excreted in the urine and faeces during the first 48 h following each treatment was assessed by direct counting of the excreta. During the same period the whole-body retention of Ra was also determined using a single probe counting system. The results of the excreta counting and the whole-body counting were compared to determine whether whole-body counting was a suitable surrogate for assessing excretion. Further whole-body retention counts were made at around 3, 4, 7 and 42 days following treatment.
RESULTS: Patterns of excretion and retention of Ra varied significantly between patients, but were similar for each patient's pair of treatments. The cumulative maximum activity excreted in the initial 8-h period following the Ra administration was 2.6% that increased to 39% at 48 h. The median excreted activity at ~1 and 6 weeks after treatment was 70 and 86%, respectively. Skeletal retention of Ra at 6 weeks ranged from 11 to 60% of the administered activity.

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Year:  2018        PMID: 29189490     DOI: 10.1097/MNM.0000000000000783

Source DB:  PubMed          Journal:  Nucl Med Commun        ISSN: 0143-3636            Impact factor:   1.690


  4 in total

Review 1.  Perspectives for Concepts of Individualized Radionuclide Therapy, Molecular Radiotherapy, and Theranostic Approaches.

Authors:  Makoto Hosono
Journal:  Nucl Med Mol Imaging       Date:  2019-01-29

2.  Dose-Dependent Growth Delay of Breast Cancer Xenografts in the Bone Marrow of Mice Treated with 223Ra: The Role of Bystander Effects and Their Potential for Therapy.

Authors:  Calvin N Leung; Brian S Canter; Didier Rajon; Tom A Bäck; J Christopher Fritton; Edouard I Azzam; Roger W Howell
Journal:  J Nucl Med       Date:  2019-09-13       Impact factor: 10.057

3.  The role of dosimetry and biological effects in metastatic castration-resistant prostate cancer (mCRPC) patients treated with 223Ra: first in human study.

Authors:  Rosa Sciuto; Sandra Rea; Sara Ungania; Antonella Testa; Valentina Dini; Maria Antonella Tabocchini; Clarice Patrono; Antonella Soriani; Valentina Palma; Raffaella Marconi; Lidia Strigari
Journal:  J Exp Clin Cancer Res       Date:  2021-09-06

4.  Radiopharmacokinetic modelling and radiation dose assessment of 223Ra used for treatment of metastatic castration-resistant prostate cancer.

Authors:  Vera Höllriegl; Nina Petoussi-Henss; Kerstin Hürkamp; Juan Camilo Ocampo Ramos; Wei Bo Li
Journal:  EJNMMI Phys       Date:  2021-06-02
  4 in total

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