ROGERIO ALEXANDRE PELISSONI
Projetos de Pesquisa
Unidades Organizacionais
Instituto do Câncer do Estado de São Paulo, Hospital das Clínicas, Faculdade de Medicina
4 resultados
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- Estimating 131I biokinetics and radiation doses to the red marrow and whole body in thyroid cancer patients: probe detection versus image quantification(2016) WILLEGAIGNON, José; PELISSONI, Rogério Alexandre; LIMA, Beatriz Christine de Godoy Diniz; SAPIENZA, Marcelo Tatit; COURA-FILHO, George Barberio; QUEIROZ, Marcelo Araújo; BUCHPIGUEL, Carlos AlbertoAbstract Objective: To compare the probe detection method with the image quantification method when estimating 131I biokinetics and radiation doses to the red marrow and whole body in the treatment of thyroid cancer patients. Materials and Methods: Fourteen patients with metastatic thyroid cancer, without metastatic bone involvement, were submitted to therapy planning in order to tailor the therapeutic amount of 131I to each individual. Whole-body scans and probe measurements were performed at 4, 24, 48, 72, and 96 h after 131I administration in order to estimate the effective half-life (Teff) and residence time of 131I in the body. Results: The mean values for Teff and residence time, respectively, were 19 ± 9 h and 28 ± 12 h for probe detection, compared with 20 ± 13 h and 29 ± 18 h for image quantification. The average dose to the red marrow and whole body, respectively, was 0.061 ± 0.041 mGy/MBq and 0.073 ± 0.040 mGy/MBq for probe detection, compared with 0.066 ± 0.055 mGy/MBq and 0.078 ± 0.056 mGy/MBq for image quantification. Statistical analysis proved that there were no significant differences between the two methods for estimating the Teff (p = 0.801), residence time (p = 0.801), dose to the red marrow (p = 0.708), and dose to the whole body (p = 0.811), even when we considered an optimized approach for calculating doses only at 4 h and 96 h after 131I administration (p > 0.914). Conclusion: There is full agreement as to the feasibility of using probe detection and image quantification when estimating 131I biokinetics and red-marrow/whole-body doses. However, because the probe detection method is inefficacious in identifying tumor sites and critical organs during radionuclide therapy and therefore liable to skew adjustment of the amount of 131I to be administered to patients under such therapy, it should be used with caution.
- Pediatric 131I-MIBG Therapy for Neuroblastoma: Whole-Body 131I-MIBG Clearance, Radiation Doses to Patients, Family Caregivers, Medical Staff, and Radiation Safety Measures(2018) WILLEGAIGNON, Jose; CREMA, Karin Paola; OLIVEIRA, Nathalie Canhameiro; PELISSONI, Rogerio Alexandre; COURA-FILHO, George Barberio; SAPIENZA, Marcelo Tatit; BUCHPIGUEL, Carlos AlbertoPurpose I-131-metaiodobenzylguanidine (I-131-MIBG) has been used in the diagnosis and therapy of neuroblastoma in adult and pediatric patients for many years. In this study, we evaluated whole-body I-131-MIBG clearance and radiation doses received by patients, family caregivers, and medical staff to establish appropriate radiation safety measures to be used in therapy applications. Methods Research was focused on 23 children and adolescents with metastatic neuroblastoma, with ages ranging from 1.8 to 13 years, being treated with I-131-MIBG. Based on measured external dose rates from patients, dosimetric data to patients, family members, and others were calculated. Results The mean SD I-131-MIBG activity administered was 8.55 +/- 1.69 GBq. Percent whole-body retention rates of I-131-MIBG at 24, 48, and 72 hours after administration were 48% +/- 7%, 23% +/- 7%, and 12% +/- 6%, with a whole-body I-131-MIBG effective half-life of 23 +/- 5 hours for all patients. The mean doses for patients were 0.234 +/- 0.096 mGyMBq(-1) to red-marrow and 0.251 +/- 0.101 mGyMBq(-1) to whole body. The maximum potential radiation doses transmitted by patients to others at 1.0 m was estimated to be 11.9 +/- 3.4 mSv, with 97% of this dose occurring over 120 hours after therapy administration. Measured mean dose received by the 22 family caregivers was 1.88 +/- 1.85 mSv, and that received by the 19 pediatric physicians was 43 +/- 51 Sv. Conclusion In this study, we evaluated the whole-body clearance of I-131-MIBG in 23 pediatric patients, and the radiation doses received by family caregivers and medical staff during these therapy procedures, thus facilitating the establishment of radiation safety measures to be applied in pediatric therapy.
- Prediction of iodine-131 biokinetics and radiation doses from therapy on the basis of tracer studies: an important question for therapy planning in nuclear medicine(2016) WILLEGAIGNON, Jose; PELISSONI, Rogerio A.; LIMA, Beatriz C. G. D.; SAPIENZA, Marcelo T.; COURA-FILHO, George B.; BUCHPIGUEL, Carlos A.ObjectivesThis study aimed to present a comparison of iodine-131 (I-131) biokinetics and radiation doses to red-marrow (rm) and whole-body (wb), following the administration of tracer and therapeutic activities, as a means of confirming whether I-131 clearance and radiation doses for therapy procedures can be predicted by tracer activities.MethodsEleven differentiated thyroid cancer patients were followed after receiving tracer and therapeutic I-131 activity. Whole-body I-131 clearance was estimated using radiation detectors and OLINDA/EXM software was used to calculate radiation doses to rm and wb.Results and discussionTracer I-131 activity of 86 (14)MBq and therapeutic activity of 8.04 (+/- 1.18)GBq were administered to patients, thereby producing an average wb I-131 effective half-time and residence time of, respectively, 13.51 (+/- 4.05) and 23.13 (+/- 5.98)h for tracer activities and 13.32 (+/- 3.38) and 19.63 (+/- 4.77)h for therapy. Radiation doses to rm and wb were, respectively, 0.0467 (+/- 0.0208) and 0.0589 (+/- 0.0207)mGy/MBq in tracer studies and 0.0396 (+/- 0.0169) and 0.0500 (+/- 0.0163)mGy/MBq in therapy. Although the differences were not considered statistically significant between averages, those between the values of effective half-times (P=0.906), residence times (P=0.145), and radiation doses to rm (P=0.393) and to wb (P=0.272), from tracer and therapy procedures, large differences of up to 80% in wb I-131 clearance, and up to 50% in radiation doses were observed when patients were analyzed individually, thus impacting on the total amount of I-131 activity calculated to be safe for application in individual therapy.Conclusion(131)I biokinetics and radiation doses to rm and wb in therapy procedures are well predicted by diagnostic activities when average values of a group of patients are compared. Nonetheless, when patients are analyzed individually, significant differences may be encountered, thus implying that nuclear medicine therapy-planning requires due consideration of changes in individual patient-body status from initial tracer to final therapy procedures to thus provide appropriate adjustments in therapeutic activities.
- Radiation safety measures in diagnostic nuclear medicine, based on the potential radiation dose emitted by radioactive patients(2023) WILLEGAIGNON, José; FERNANDES, Samantha Cristina Pereira; PELISSONI, Rogério Alexandre; COURA-FILHO, George Barbério; SAPIENZA, Marcelo Tatit; BUCHPIGUEL, Carlos AlbertoAbstract Objective: To measure the potential radiation dose emitted by patients who have recently undergone diagnostic nuclear medicine procedures, in order to establish optimal radiation safety measures for such procedures. Materials and Methods: We evaluated the radiation doses emitted by 175 adult patients in whom technetium-99m, iodine-131, and fluorine-18 radionuclides were administered for bone, kidney, heart, brain, and whole-body scans, as measured with a radiation detector. Those values served as the basis for evaluating whole-body radiopharmaceutical clearance, as well as the risk for the exposure of others to radiation, depending on the time elapsed since administration of the radiopharmaceutical. Results: The mean time to clearance of the radiopharmaceuticals administered, expressed as the effective half-life, ranged from 1.18 ± 0.30 h to 11.41 ± 0.02 h, and the mean maximum cumulative radiation dose at 1.0 m from the patients was 149.74 ± 56.72 µSv. Even at a distance of 0.5 m, the cumulative dose was found to be only half and one tenth of the limits established for exposure of the general public and family members/caregivers (1.0 mSv and 5.0 mSv per episode, respectively). Conclusion: Cumulative radiation doses emitted by patients immediately after diagnostic nuclear medicine procedures are considerably lower than the limits established by the International Commission on Radiological Protection and the International Atomic Energy Agency, and precautionary measures to avoid radiation exposure are therefore not required after such procedures.