MARCELO TATIT SAPIENZA

(Fonte: Lattes)
Índice h a partir de 2011
14
Projetos de Pesquisa
Unidades Organizacionais
Departamento de Radiologia, Faculdade de Medicina - Docente
Instituto de Radiologia, Hospital das Clínicas, Faculdade de Medicina
LIM/43 - Laboratório de Medicina Nuclear, Hospital das Clínicas, Faculdade de Medicina

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  • article 8 Citação(ões) na Scopus
    Hot needles can confirm accurate lesion sampling intraoperatively using [F-18]PSMA-1007 PET/CT-guided biopsy in patients with suspected prostate cancer
    (2022) FERRARO, Daniela A.; LAUDICELLA, Riccardo; ZEIMPEKIS, Konstantinos; MEBERT, Iliana; MUELLER, Julian; MAURER, Alexander; GRUENIG, Hannes; DONATI, Olivio; SAPIENZA, Marcelo T.; RUESCHOFF, Jan H.; RUPP, Niels; EBERLI, Daniel; BURGER, Irene A.
    Purpose Prostate-specific membrane antigen (PSMA)-targeted PET is increasingly used for staging prostate cancer (PCa) with high accuracy to detect significant PCa (sigPCa). [(68) Ga]PSMA-11 PET/MRI-guided biopsy showed promising results but also persisting limitation of sampling error, due to impaired image fusion. We aimed to assess the possibility of intraoperative quantification of [F-18]PSMA-1007 PET/CT uptake in core biopsies as an instant confirmation for accurate lesion sampling. Methods In this IRB-approved, prospective, proof-of-concept study, we included five consecutive patients with suspected PCa. All underwent [F-18]PSMA-1007 PET/CT scans followed by immediate PET/CT-guided and saturation template biopsy (3.1 +/- 0.3 h after PET). The activity in biopsy cores was measured as counts per minute (cpm) in a gamma spectrometer. Pearson's test was used to correlate counts with histopathology (WHO/ISUP), tumor length, and membranous PSMA expression on immunohistochemistry (IHC). Results In 43 of 113 needles, PCa was present. The mean cpm was overall significantly higher in needles with PCa (263 +/- 396 cpm) compared to needles without PCa (73 +/- 44 cpm, p < 0.001). In one patient with moderate PSMA uptake (SUVmax 8.7), 13 out of 24 needles had increased counts (100-200 cpm) but only signs of inflammation and PSMA expression in benign glands on IHC. Excluding this case, ROC analysis resulted in an AUC of 0.81, with an optimal cut-off to confirm PCa at 75 cpm (sens/spec of 65.1%/87%). In all 4 patients with PCa, the first or second PSMA PET-guided needle was positive for sigPCa with high counts (156-2079 cpm). Conclusions [F-18]PSMA-1007 uptake in PCa can be used to confirm accurate lesion sampling of the dominant tumor intraoperatively. This technique could improve confidence in imaging-based biopsy guidance and reduce the need for saturation biopsy.
  • article 12 Citação(ões) na Scopus
    Graves' disease radioiodine-therapy: Choosing target absorbed doses for therapy planning
    (2014) WILLEGAIGNON, J.; SAPIENZA, M. T.; COURA-FILHO, G. B.; WATANABE, T.; TRAINO, A. C.; BUCHPIGUEL, C. A.
    Purpose: The precise determination of organ mass (m(th)) and total number of disintegrations within the thyroid gland ((A) over tilde) are essential for thyroid absorbed-dose calculations for radioiodine therapy. Nevertheless, these parameters may vary according to the method employed for their estimation, thus introducing uncertainty in the estimated thyroid absorbed dose and in any dose-response relationship derived using such estimates. In consideration of these points, thyroid absorbed doses for Graves' disease (GD) treatment planning were calculated using different approaches to estimating the m(th) and the (A) over tilde. Methods: Fifty patients were included in the study. Thyroid I-131 uptake measurements were performed at 2, 6, 24, 48, 96, and 220 h postadministration of a tracer activity in order to estimate the effective half-time (T-eff) of I-131 in the thyroid; the thyroid cumulated activity was then estimated using the Teff thus determined or, alternatively, calculated by numeric integration of the measured time-activity data. Thyroid mass was estimated by ultrasonography (USG) and scintigraphy (SCTG). Absorbed doses were calculated with the OLINDA/EXM software. The relationships between thyroid absorbed dose and therapy response were evaluated at 3 months and 1 year after therapy. Results: The average ratio (+/- 1 standard deviation) between m(th) estimated by SCTG and USG was 1.74 (+/- 0.64) and that between (A) over tilde obtained by Teff and the integration of measured activity in the gland was 1.71 (+/- 0.14). These differences affect the calculated absorbed dose. Overall, therapeutic success, corresponding to induction of durable hypothyroidism or euthyroidism, was achieved in 72% of all patients at 3 months and in 90% at 1 year. A therapeutic success rate of at least 95% was found in the group of patients receiving doses of 200 Gy (p = 0.0483) and 330 Gy (p = 0.0131) when m(th) was measured by either USG or SCTG and (A) over tilde was determined by the integration of measured I-131 activity in the thyroid gland and based on T-eff, respectively. No statistically significant relationship was found between therapeutic response and patients' age, administered I-131 activity (MBq), 24-h thyroid I-131 uptake (%) or T-eff (p >= 0.064); nonetheless, a good relationship was found between the therapeutic response and mth (p >= 0.035). Conclusions: According to the results of this study, the most effective thyroid absorbed dose to be targeted in GD therapy should not be based on a fixed dose but rather should be individualized based on the patient's m(th) and (A) over tilde. To achieve a therapeutic success (i.e., durable euthyroidism or hypothyroidism) rate of at least 95%, a thyroid absorbed dose of 200 or 330 Gy is required depending on the methodology used for estimating m(th) and (A) over tilde. (C) 2014 American Association of Physicists in Medicine.
  • conferenceObject
    Hot needles can confirm accurate lesion sampling intraoperatively using [F-18]PSMA-1007 PET guided biopsy in patients with suspected prostate cancer
    (2021) LAUDICELLA, R.; FERRARO, D. A.; ZEIMPEKIS, K. G.; MEBERT, I.; MUELLER, J.; DONATI, O.; SAPIENZA, M. T.; RUSCHOFF, J. H.; RUPP, N.; EBERLI, D.; BURGER, I. A.
  • article 6 Citação(ões) na Scopus
    Ga-68-PSMA-11 PET/MRI versus multiparametric MRI in men referred for prostate biopsy: primary tumour localization and interreader agreement
    (2022) FERRARO, Daniela A.; HOETKER, Andreas M.; BECKER, Anton S.; MEBERT, Iliana; LAUDICELLA, Riccardo; BALTENSPERGER, Anka; RUPP, Niels J.; RUESCHOFF, Jan H.; MUELLER, Julian; MORTEZAVI, Ashkan; SAPIENZA, Marcelo T.; EBERLI, Daniel; DONATI, Olivio F.; BURGER, Irene A.
    Background Magnetic resonance imaging (MRI) is recommended by the European Urology Association guidelines as the standard modality for imaging-guided biopsy. Recently positron emission tomography with prostate-specific membrane antigen (PSMA PET) has shown promising results as a tool for this purpose. The aim of this study was to compare the accuracy of positron emission tomography with prostate-specific membrane antigen/magnetic resonance imaging (PET/MRI) using the gallium-labeled prostate-specific membrane antigen (Ga-68-PSMA-11) and multiparametric MRI (mpMRI) for pre-biopsy tumour localization and interreader agreement for visual and semiquantitative analysis. Semiquantitative parameters included apparent diffusion coefficient (ADC) and maximum lesion diameter for mpMRI and standardized uptake value (SUVmax) and PSMA-positive volume (PSMA(vol)) for PSMA PET/MRI. Results Sensitivity and specificity were 61.4% and 92.9% for mpMRI and 66.7% and 92.9% for PSMA PET/MRI for reader one, respectively. RPE was available in 23 patients and 41 of 47 quadrants with discrepant findings. Based on RPE results, the specificity for both imaging modalities increased to 98% and 99%, and the sensitivity improved to 63.9% and 72.1% for mpMRI and PSMA PET/MRI, respectively. Both modalities yielded a substantial interreader agreement for primary tumour localization (mpMRI kappa = 0.65 (0.52-0.79), PSMA PET/MRI kappa = 0.73 (0.61-0.84)). ICC for SUVmax, PSMA(vol) and lesion diameter were almost perfect (>= 0.90) while for ADC it was only moderate (ICC = 0.54 (0.04-0.78)). ADC and lesion diameter did not correlate significantly with Gleason score (rho = 0.26 and rho = 0.16) while SUVmax and PSMA(vol) did (rho = - 0.474 and rho = - 0.468). Conclusions PSMA PET/MRI has similar accuracy and reliability to mpMRI regarding primary prostate cancer (PCa) localization. In our cohort, semiquantitative parameters from PSMA PET/MRI correlated with tumour grade and were more reliable than the ones from mpMRI.
  • article 10 Citação(ões) na Scopus
    Determining thyroid I-131 effective half-life for the treatment planning of Graves' disease
    (2013) WILLEGAIGNON, Jose; SAPIENZA, Marcelo T.; COURA FILHO, George Barberio; TRAINO, Antonio C.; BUCHPIGUEL, Carlos A.
    Purpose: Thyroid I-131 effective half-life (T-eff) is an essential parameter in patient therapy when accurate radiation dose is desirable for producing an intended therapeutic outcome. Multiple I-131 uptake measurements and resources from patients themselves and from nuclear medicine facilities are requisites for determining T-eff, these being limiting factors when implementing the treatment planning of Graves' disease (GD) in radionuclide therapy. With the aim of optimizing this process, this study presents a practical, propitious, and accurate method of determining T-eff for dosimetric purposes. Methods: A total of 50 patients with GD were included in this prospective study. Thyroidal I-131 uptake was measured at 2-h, 6-h, 24-h, 48-h, 96-h, and 220-h postradioiodine administration. T-eff was calculated by considering sets of two measured points (24-48-h, 24-96-h, and 24-220-h), sets of three (24-48-96-h, 24-48-220-h, and 24-96-220-h), and sets of four (24-48-96-220-h). Results: When considering all the measured points, the representative T-eff for all the patients was 6.95 (+/- 0.81) days, whereas when using such sets of points as (24-220-h), (24-96-220-h), and (24-48-220-h), this was 6.85 (+/- 0.81), 6.90 (+/- 0.81), and 6.95 (+/- 0.81) days, respectively. According to the mean deviations 2.2 (+/- 2.4)%, 2.1 (+/- 2.0)%, and 0.04 (+/- 0.09)% found in T-eff, calculated based on all the measured points in time, and with methods using the (24-220-h), (24-48-220-h), and (24-96-220-h) sets, respectively, no meaningful statistical difference was noted among the three methods (p > 0.500, t test). Conclusions: T-eff obtained from only two thyroid I-131 uptakes measured at 24-h and 220-h, besides proving to be sufficient, accurate enough, and easily applicable, attributes additional major cost-benefits for patients, and facilitates the application of the method for dosimetric purposes in the treatment planning of Graves' disease. (c) 2013 American Association of Physicists in Medicine. [http://dx.doi.org/10.1118/1.4788660]