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Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients

BACKGROUND: To evaluate the prevalence, density, and distribution of prostate calcification in patients with prostate cancer. METHODS: Patients who underwent both Gallium-68 PSMA PET/CT and MRI of the prostate over the course of a year were selected for analysis. The CT images with visible calcifica...

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Autores principales: Singh, Saurabh, Martin, Eleanor, Tregidgo, Henry F.J., Treeby, Bradley, Bandula, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492071/
https://www.ncbi.nlm.nih.gov/pubmed/33485763
http://dx.doi.org/10.1016/j.urolonc.2020.12.028
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author Singh, Saurabh
Martin, Eleanor
Tregidgo, Henry F.J.
Treeby, Bradley
Bandula, Steve
author_facet Singh, Saurabh
Martin, Eleanor
Tregidgo, Henry F.J.
Treeby, Bradley
Bandula, Steve
author_sort Singh, Saurabh
collection PubMed
description BACKGROUND: To evaluate the prevalence, density, and distribution of prostate calcification in patients with prostate cancer. METHODS: Patients who underwent both Gallium-68 PSMA PET/CT and MRI of the prostate over the course of a year were selected for analysis. The CT images with visible calcifications within the prostate were included and calcifications automatically isolated using a threshold of 130 HU. The corresponding multiparametric MRI was assessed and the peripheral zone, transition zone, MRI-visible tumor, and urethra manually contoured. The contoured MRI and CT images were registered using rigid registration, and calcifications mapped automatically to the MRI contours. RESULTS: A total of 85 men (age range 50–88, mean 69 years, standard deviation 7.2 years) were assessed. The mean serum Prostate Specific Antigen PSA was 16.7, range 0.12 to 94.4. Most patients had intermediate-risk disease (68%; Gleason grade group 2 and 3), 26% had high-risk disease (Gleason grade group 4 and 5), and 6% had low-risk disease (Gleason grade group 1). Forty-six patients out of 85 (54%) had intraprostatic calcification. Calcification occurred more in transition zone than the peripheral zone (65% vs. 35%). The mean density of the calcification was 227 HU (min 133, max 1,966 HU). In 12 patients, the calcification was within an MRI-visible tumor, in 24 patients, there were calcifications within a 9 mm distance of the tumor border, and in 9 patients, there were calcifications located between the urethra and tumor. CONCLUSIONS: Calcifications are common in patients with prostate cancer. Their density and location may make them a significant consideration when planning treatment or retreatment with some types of minimally invasive therapy.
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spelling pubmed-84920712021-10-08 Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients Singh, Saurabh Martin, Eleanor Tregidgo, Henry F.J. Treeby, Bradley Bandula, Steve Urol Oncol Clinical-Prostate cancer BACKGROUND: To evaluate the prevalence, density, and distribution of prostate calcification in patients with prostate cancer. METHODS: Patients who underwent both Gallium-68 PSMA PET/CT and MRI of the prostate over the course of a year were selected for analysis. The CT images with visible calcifications within the prostate were included and calcifications automatically isolated using a threshold of 130 HU. The corresponding multiparametric MRI was assessed and the peripheral zone, transition zone, MRI-visible tumor, and urethra manually contoured. The contoured MRI and CT images were registered using rigid registration, and calcifications mapped automatically to the MRI contours. RESULTS: A total of 85 men (age range 50–88, mean 69 years, standard deviation 7.2 years) were assessed. The mean serum Prostate Specific Antigen PSA was 16.7, range 0.12 to 94.4. Most patients had intermediate-risk disease (68%; Gleason grade group 2 and 3), 26% had high-risk disease (Gleason grade group 4 and 5), and 6% had low-risk disease (Gleason grade group 1). Forty-six patients out of 85 (54%) had intraprostatic calcification. Calcification occurred more in transition zone than the peripheral zone (65% vs. 35%). The mean density of the calcification was 227 HU (min 133, max 1,966 HU). In 12 patients, the calcification was within an MRI-visible tumor, in 24 patients, there were calcifications within a 9 mm distance of the tumor border, and in 9 patients, there were calcifications located between the urethra and tumor. CONCLUSIONS: Calcifications are common in patients with prostate cancer. Their density and location may make them a significant consideration when planning treatment or retreatment with some types of minimally invasive therapy. Elsevier 2021-10 /pmc/articles/PMC8492071/ /pubmed/33485763 http://dx.doi.org/10.1016/j.urolonc.2020.12.028 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Clinical-Prostate cancer
Singh, Saurabh
Martin, Eleanor
Tregidgo, Henry F.J.
Treeby, Bradley
Bandula, Steve
Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title_full Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title_fullStr Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title_full_unstemmed Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title_short Prostatic calcifications: Quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
title_sort prostatic calcifications: quantifying occurrence, radiodensity, and spatial distribution in prostate cancer patients
topic Clinical-Prostate cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492071/
https://www.ncbi.nlm.nih.gov/pubmed/33485763
http://dx.doi.org/10.1016/j.urolonc.2020.12.028
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