Abstract

BackgroundCurrently, the implementation of dosimetry in molecular radiotherapy (MRT) is not well investigated, and in view of the Council Directive (2013/59/Euratom), there is a need to understand the current availability of dosimetry-based MRT in clinical practice and research studies. The aim of this study was to assess the current practice of MRT and dosimetry across European countries.MethodsAn electronic questionnaire was distributed to European countries. This addressed 18 explicitly considered therapies, and for each therapy, a similar set of questions were included. Questions covered the number of patients and treatments during 2015, involvement of medical specialties and medical physicists, implementation of absorbed dose planning, post-therapy imaging and dosimetry, and the basis of therapy prescription.ResultsResponses were obtained from 26 countries and 208 hospitals, administering in total 42,853 treatments. The most common therapies were 131I-NaI for benign thyroid diseases and thyroid ablation of adults. The involvement of a medical physicist (mean over all 18 therapies) was reported to be either minority or never by 32% of the responders. The percentage of responders that reported that dosimetry was included on an always/majority basis differed between the therapies and showed a median value of 36%. The highest percentages were obtained for 177Lu-PSMA therapy (100%), 90Y microspheres of glass (84%) and resin (82%), 131I-mIBG for neuroblastoma (59%), and 131I-NaI for benign thyroid diseases (54%). The majority of therapies were prescribed based on fixed-activity protocols. The highest number of absorbed-dose based prescriptions were reported for 90Y microsphere treatments in the liver (64% and 96% of responses for resin and glass, respectively), 131I-NaI treatment of benign thyroid diseases (38% of responses), and for 131I-mIBG treatment of neuroblastoma (18% of responses).ConclusionsThere is a wide variation in MRT practice across Europe and for different therapies, including the extent of medical-physicist involvement and the implementation of dosimetry-guided treatments.

Highlights

  • The implementation of dosimetry in molecular radiotherapy (MRT) is not well investigated, and in view of the Council Directive (2013/59/Euratom), there is a need to understand the current availability of dosimetry-based MRT in clinical practice and research studies

  • Initial reports of MRT in humans date back to the period between 1938 and 1939, when several patients suffering from chronic myeloid and lymphoid leukemia were treated with repeated oral administrations of 32P sodium phosphate, which accumulates in blood cells [1]

  • The survey was developed by the Internal Dosimetry Task Force (IDTF) and focused on treatments given during the year 2015

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Summary

Introduction

The implementation of dosimetry in molecular radiotherapy (MRT) is not well investigated, and in view of the Council Directive (2013/59/Euratom), there is a need to understand the current availability of dosimetry-based MRT in clinical practice and research studies. Molecular radiotherapy (MRT) refers to the use of internally distributed, unsealed radioactive substances for the treatment of benign and malignant diseases. These radioactive substances, namely radiopharmaceuticals, represent the combination of an unstable radionuclide with an active or pharmacologically inert molecule. Therapeutic radiopharmaceuticals are often administered intravenously, oral, intra-cavity, and intra-arterial administrations are employed. They are designed to accumulate in a target tissue and, if administered systemically, are able to simultaneously treat disseminated disease which represents a clear advantage over other more localized radiotherapy modalities. Based on the results of such measurements, the distribution of activity and absorbed dose can be individually determined for the relevant organs and target tissues

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