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Phys Med Biol. 2017 Mar 7;62(5):1885-1904. doi: 10.1088/1361-6560/62/5/1885. Epub 2017 Feb 9.

Internal dosimetry with the Monte Carlo code GATE: validation using the ICRP/ICRU female reference computational model.

Author information

1
Inserm, UMR1037 CRCT, F-31000 Toulouse, France. Université Toulouse III-Paul Sabatier, UMR1037 CRCT, F-31000 Toulouse, France.

Abstract

The purpose of this work was to validate GATE-based clinical scale absorbed dose calculations in nuclear medicine dosimetry. GATE (version 6.2) and MCNPX (version 2.7.a) were used to derive dosimetric parameters (absorbed fractions, specific absorbed fractions and S-values) for the reference female computational model proposed by the International Commission on Radiological Protection in ICRP report 110. Monoenergetic photons and electrons (from 50 keV to 2 MeV) and four isotopes currently used in nuclear medicine (fluorine-18, lutetium-177, iodine-131 and yttrium-90) were investigated. Absorbed fractions, specific absorbed fractions and S-values were generated with GATE and MCNPX for 12 regions of interest in the ICRP 110 female computational model, thereby leading to 144 source/target pair configurations. Relative differences between GATE and MCNPX obtained in specific configurations (self-irradiation or cross-irradiation) are presented. Relative differences in absorbed fractions, specific absorbed fractions or S-values are below 10%, and in most cases less than 5%. Dosimetric results generated with GATE for the 12 volumes of interest are available as supplemental data. GATE can be safely used for radiopharmaceutical dosimetry at the clinical scale. This makes GATE a viable option for Monte Carlo modelling of both imaging and absorbed dose in nuclear medicine.

PMID:
28182580
DOI:
10.1088/1361-6560/62/5/1885
[Indexed for MEDLINE]

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