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Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients

PURPOSE: The aim of this study is to assess the usefulness of perfusion computer tomography (pCT) in prostate cancer (PCa) diagnostics. MATERIALS AND METHODS: 94 patients with biopsy-proven PCa were enrolled in the study. Dynamic pCT of the prostate gland was performed for 50 seconds after an intrav...

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Autores principales: Luczynska, Elzbieta, Blecharz, Pawel, Dyczek, Sonia, Stelmach, Andrzej, Petralia, Giuseppe, Bellomi, Massimo, Jereczek–Fossa, Barbara Alicja, Jakubowicz, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239130/
https://www.ncbi.nlm.nih.gov/pubmed/25435904
http://dx.doi.org/10.3332/ecancer.2014.476
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author Luczynska, Elzbieta
Blecharz, Pawel
Dyczek, Sonia
Stelmach, Andrzej
Petralia, Giuseppe
Bellomi, Massimo
Jereczek–Fossa, Barbara Alicja
Jakubowicz, Jerzy
author_facet Luczynska, Elzbieta
Blecharz, Pawel
Dyczek, Sonia
Stelmach, Andrzej
Petralia, Giuseppe
Bellomi, Massimo
Jereczek–Fossa, Barbara Alicja
Jakubowicz, Jerzy
author_sort Luczynska, Elzbieta
collection PubMed
description PURPOSE: The aim of this study is to assess the usefulness of perfusion computer tomography (pCT) in prostate cancer (PCa) diagnostics. MATERIALS AND METHODS: 94 patients with biopsy-proven PCa were enrolled in the study. Dynamic pCT of the prostate gland was performed for 50 seconds after an intravenous injection of contrast medium. Blood flow (BF), blood volume (BV), mean transit time (MTT) and permeability surface area product (PS) were computed in the suspected PCa area and in normal prostatic tissue. RESULTS: PCa was visible in pCT in 90 of the 94 examined patients as a focal peripheral CT enhancement. When PCa was located in the peripheral zone (PZ), it was visible on perfusion maps, mostly showing an early peak followed by wash-out. The average values of all perfusion parameters were higher for tumour than for normal prostate tissue (p < 0.000). BV and BF were dependent on tumour grade expressed by the Gleason score (GS). All PCa cases were divided into groups, according to histological grade, as low (GS ≤ 6), medium (GS = 7), and high (GS > 7). In high-grade PCa, the mean BF value was significantly higher (p = 0.001) than the mean value of BF low- and medium-grade PCa (p = 0.011). Similar results were obtained regarding the mean values of BV; the more aggressive the cancer grade, the higher the mean BV value (p = 0.04). CONCLUSION: CT quantitative perfusion imaging allows PCa to be distinguished from normal prostate tissue. The highest values for BF and BV were observed in the most aggressive PCa grade.
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spelling pubmed-42391302014-11-28 Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients Luczynska, Elzbieta Blecharz, Pawel Dyczek, Sonia Stelmach, Andrzej Petralia, Giuseppe Bellomi, Massimo Jereczek–Fossa, Barbara Alicja Jakubowicz, Jerzy Ecancermedicalscience Research PURPOSE: The aim of this study is to assess the usefulness of perfusion computer tomography (pCT) in prostate cancer (PCa) diagnostics. MATERIALS AND METHODS: 94 patients with biopsy-proven PCa were enrolled in the study. Dynamic pCT of the prostate gland was performed for 50 seconds after an intravenous injection of contrast medium. Blood flow (BF), blood volume (BV), mean transit time (MTT) and permeability surface area product (PS) were computed in the suspected PCa area and in normal prostatic tissue. RESULTS: PCa was visible in pCT in 90 of the 94 examined patients as a focal peripheral CT enhancement. When PCa was located in the peripheral zone (PZ), it was visible on perfusion maps, mostly showing an early peak followed by wash-out. The average values of all perfusion parameters were higher for tumour than for normal prostate tissue (p < 0.000). BV and BF were dependent on tumour grade expressed by the Gleason score (GS). All PCa cases were divided into groups, according to histological grade, as low (GS ≤ 6), medium (GS = 7), and high (GS > 7). In high-grade PCa, the mean BF value was significantly higher (p = 0.001) than the mean value of BF low- and medium-grade PCa (p = 0.011). Similar results were obtained regarding the mean values of BV; the more aggressive the cancer grade, the higher the mean BV value (p = 0.04). CONCLUSION: CT quantitative perfusion imaging allows PCa to be distinguished from normal prostate tissue. The highest values for BF and BV were observed in the most aggressive PCa grade. Cancer Intelligence 2014-10-27 /pmc/articles/PMC4239130/ /pubmed/25435904 http://dx.doi.org/10.3332/ecancer.2014.476 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Luczynska, Elzbieta
Blecharz, Pawel
Dyczek, Sonia
Stelmach, Andrzej
Petralia, Giuseppe
Bellomi, Massimo
Jereczek–Fossa, Barbara Alicja
Jakubowicz, Jerzy
Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title_full Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title_fullStr Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title_full_unstemmed Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title_short Perfusion CT is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
title_sort perfusion ct is a valuable diagnostic method for prostate cancer: a prospective study of 94 patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4239130/
https://www.ncbi.nlm.nih.gov/pubmed/25435904
http://dx.doi.org/10.3332/ecancer.2014.476
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