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Safety of gadolinium based contrast agents in magnetic resonance imaging-guided radiotherapy – An investigation of chelate stability using relaxometry

BACKGROUND AND PURPOSE: With the introduction of hybrid magnetic resonance linacs (MR-linac), improved imaging has enabled daily treatment adaptation. However, the use of gadolinium based contrast agents (GBCAs) is desired to further improve MR image contrast. GBCAs are in the form of a non-toxic me...

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Detalles Bibliográficos
Autores principales: Mahmood, Faisal, Nielsen, Ulla Gro, Jørgensen, Christian Brandt, Brink, Carsten, Thomsen, Henrik S., Hansen, Rasmus Hvass
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885577/
https://www.ncbi.nlm.nih.gov/pubmed/35243039
http://dx.doi.org/10.1016/j.phro.2022.02.015
Descripción
Sumario:BACKGROUND AND PURPOSE: With the introduction of hybrid magnetic resonance linacs (MR-linac), improved imaging has enabled daily treatment adaptation. However, the use of gadolinium based contrast agents (GBCAs) is desired to further improve MR image contrast. GBCAs are in the form of a non-toxic metalorganic gadolinium complex, but toxic un-chelated aqueous gadolinium(III), Gd(3+)(aq), can be released in patients if the organic ligand is degraded by the radiation. In this study, T(1) relaxation measurements were performed to study the effect of radiation on three GBCAs. MATERIALS AND METHODS: GBCAs, gadoteric acid, gadobutrol and gadoxectic acid were investigated in a concentration range of 10–100 mM. Measurements were performed on a 500 MHz nuclear MR (NMR) spectrometer with a high-resolution inversion recovery sequence to determine T(1). Samples were irradiated with 7 MV photons on an MR-linac to a total dose of 100 Gy. The lower detection limit of Gd(3+)(aq) was established by estimating the overall measurement uncertainty and comparing to corresponding changes in R(1) when replacing chelated Gd(3+) with gadolinium nitrate at predefined percentages. RESULTS: The overall measurement uncertainty was estimated to ±0.0053 ms(−1), corresponding to Gd(3+)(aq) detection levels 1%–1.5% or 1–4.5 micro molar at clinical GBCA dosage. No detectable differences in R(1) were observed between irradiated and non-irradiated samples for any GBCA. CONCLUSIONS: This study did not find any measurable degradation of GBCAs due to irradiation with high-energy X-rays, however, in-vivo investigations are needed to provide the clinical basis for safe use of contrast agents in a radiotherapy workflow.