JOSE WILLEGAIGNON DE AMORIM DE CARVALHO
Projetos de Pesquisa
Unidades Organizacionais
LIM/43 - Laboratório de Medicina Nuclear, Hospital das Clínicas, Faculdade de Medicina
5 resultados
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conferenceObject Case study: Evaluating the new University of Florida hybrid pediatric phantoms and tissue weighting factors from ICRP Publication 103 for diagnostic dosimetry(2018) JOSEFSSON, Anders; HOBBS, Robert; RANKA, Sagar; SCHWARZ, Bryan; CARVALHO, Jose Willegaignon de Amorim de; BUCHPIGUEL, Carlos Alberto; SAPIENZA, Marcelo Tatit; BOLCH, Wesley; SGOUROS, George- Influence on voxel-based dosimetry: noise effect on absorbed dose dosimetry at single time-point versus sequential single-photon emission computed tomography(2023) FONDA, Uysha de S.; LEITAO, Andre L. A.; PAIVA, Marcia M. D. P.; WILLEGAIGNON, Jose; JOSEFSSON, Anders; BUCHPIGUEL, Carlos A.; SAPIENZA, Marcelo T.ObjectiveThe purpose of this study was to evaluate how statistical fluctuation in single-photon emission computed tomography (SPECT) images propagate to absorbed dose maps. MethodsSPECT/computed tomography (CT) images of iodine-131 filled phantoms, using different acquisition and processing protocols, were evaluated using STRATOS software to assess the absorbed dose distribution at the voxel level. Absorbed dose values and coefficient of variation (COV) were analyzed for dosimetry based on single time-point SPECT images and time-integrated activities of SPECT sequences with low and high counts. ResultsConsidering dosimetry based on a single time-point, the mean absorbed dose was not significantly affected by total counts or reconstruction parameters, but the uniformity of the absorbed dose maps had an almost linear correlation with SPECT noise. When high- and low-count SPECT sequences were used to generate an absorbed dose map, the absorbed dose COV for each of the temporal sequences was slightly lower than the absorbed dose COV based on the single SPECT image with the highest count included in the sequence. ConclusionThe impact of changes in SPECT counts and reconstruction parameters is almost linear when dosimetry is based on isolated SPECT images, but less pronounced when dosimetry is based on sequential SPECTs.
- Accuracy in dosimetry of diagnostic agents: impact of the number of source tissues used in whole organ S value-based calculations(2020) JOSEFSSON, Anders; SIRITANTIKORN, Klaikangwol; RANKA, Sagar; CARVALHO, Jose Willegaignon de Amorim de; BUCHPIGUEL, Carlos Alberto; SAPIENZA, Marcelo Tatit; BOLCH, Wesley E.; SGOUROS, GeorgeBackground Dosimetry for diagnostic agents is performed to assess the risk of radiation detriment (e.g., cancer) associated with the imaging agent and the risk is assessed by computing the effective dose coefficient, e. Stylized phantoms created by the MIRD Committee and updated by work performed by Cristy-Eckerman (CE) have been the standard in diagnostic dosimetry. Recently, the ICRP developed voxelized phantoms, which are described in ICRP Publication 110. These voxelized phantoms are more realistic and detailed in describing human anatomy compared with the CE stylized phantoms. Ideally, all tissues should be represented and their pharmacokinetics collected for an as accurate a dosimetric calculation as possible. As the number of source tissues included increases, the calculated e becomes more accurate. There is, however, a trade-off between the number of source tissues considered, and the time and effort required to measure the time-activity curve for each tissue needed for the calculations. In this study, we used a previously published Ga-68-DOTA-TATE data set to examine how the number of source tissues included for both the ICRP voxelized and CE stylized phantoms affected e. Results Depending upon the number of source tissues included e varied between 14.0-23.5 mu Sv/MBq for the ICRP voxelized and 12.4-27.7 mu Sv/MBq for the CE stylized phantoms. Furthermore, stability in e, defined as a < 10% difference between e obtained using all source tissues compared to one using fewer source tissues, was obtained after including 5 (36%) of the 14 source tissues for the ICRP voxelized, and after including 3 (25%) of the 12 source tissues for the CE stylized phantoms. In addition, a 2-fold increase in e was obtained when all source tissues where included in the calculation compared to when the TIAC distribution was lumped into a single reminder-of-body source term. Conclusions This study shows the importance of including the larger tissues like the muscles and remainder-of-body in the dosimetric calculations. The range of e based on the included tissues were less for the ICRP voxelized phantoms using tissue weighting factors from ICRP Publication 103 compared to CE stylized phantoms using tissue weighting factors from ICRP Publication 60.
conferenceObject Predicting dosimetry for therapy using imaging analogs of therapeutic radiopharmaceuticals: An uncertainty and sensitivity analysis applicable to Theranostics(2015) JOSEFSSON, Anders; HOBBS, Robert; PLYKU, Donika; HUANG, Kevin; WILLEGAIGNON, Jose; COURA FILHO, George; DUARTE, Paulo; SAPIENZA, Marcelo; SGOUROS, George- Comparative Dosimetry for Ga-68-DOTATATE: Impact of Using Updated ICRP Phantoms, S Values, and Tissue-Weighting Factors(2018) JOSEFSSON, Anders; HOBBS, Robert F.; RANKA, Sagar; SCHWARZ, Bryan C.; PLYKU, Donika; CARVALHO, Jose Willegaignon de Amorim de; BUCHPIGUEL, Carlos Alberto; SAPIENZA, Marcelo Tatit; BOLCH, Wesley E.; SGOUROS, GeorgeThe data that have been used in almost all calculations of MIRD S value absorbed dose and effective dose are based on stylized anatomic computational phantoms and tissue-weighting factors adopted by the International Commission on Radiological Protection (ICRP) in its publication 60. The more anatomically realistic phantoms that have recently become available are likely to provide more accurate effective doses for diagnostic agents. Ga-68-DOTATATE is a radiolabeled somatostatin analog that binds with high affinity to somatostatin receptors, which are overexpressed in neuroendocrine tumors and can be used for diagnostic PET/CT-based imaging. Several studies have reported effective doses for Ga-68-DOTATATE using the stylized Cristy-Eckerman (CE) phantoms from 1987; here, we present effective dose calculations using both the ICRP 60 and more updated formalisms. Methods: Whole-body PET/CT scans were acquired for 16 patients after Ga-68-DOTATATE administration. Contours were drawn on the CT images for spleen, liver, kidneys, adrenal glands, brain, heart, lungs, thyroid gland, salivary glands, testes, red marrow (L1-L5), muscle (right thigh), and whole body. Dosimetric calculations were based on the CE phantoms and the more recent ICRP 110 reference-voxel phantoms. Tissue-weighting factors from ICRP 60 and ICRP 103 were used in effective dose calculations for the CE phantoms and ICRP 110 phantoms, respectively. Results: The highest absorbed dose coefficients (absorbed dose per unit activity) were, in descending order, in the spleen, pituitary gland, kidneys, adrenal glands, and liver. For ICRP 110 phantoms with tissue-weighting factors from ICRP 103, the effective dose coefficient was 0.023 +/- 0.003 mSv/MBq, which was significantly lower than the 0.027 +/- 0.005 mSv/MBq calculated for CE phantoms with tissue-weighting factors from ICRP 60. One of the largest differences in estimated absorbed dose coefficients was for the urinary bladder wall, at 0.040 +/- 0.011 mGy/MBq for ICRP 110 phantoms compared with 0.090 +/- 0.032 mGy/MBq for CE phantoms. Conclusion: This study showed that the effective dose coefficient was slightly overestimated for CE phantoms, compared with ICRP 110 phantoms using the latest tissue-weighting factors from ICRP 103. The more detailed handling of electron transport in the latest phantom calculations gives significant differences in estimates of the absorbed dose to stem cells in the walled organs of the alimentary tract.