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PHI in the Early Detection of Prostate Cancer
R. Fuchsova, O. Topolcan, J. Windrichova, M. Hora, O. Dolejsova, L. Pecen, P. Kasik, J. Novak, M. Casova, J. Smejkal,
Jazyk angličtina Země Řecko
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 2004 do Před 2 roky
Open Access Digital Library
od 2004-01-01
PubMed
26254378
Knihovny.cz E-zdroje
- MeSH
- časná detekce nádoru MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery krev MeSH
- nádory prostaty krev diagnóza MeSH
- plocha pod křivkou MeSH
- prostata patologie MeSH
- prostatický specifický antigen krev MeSH
- ROC křivka MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- senzitivita a specificita MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
AIM: To evaluate changes in the serum levels of prostate specific antigen (PSA), %free PSA and -2proPSA biomarkers, and prostate health index (PHI) in the diagnostic algorithm of early prostate cancer. PATIENTS AND METHODS: The Immunoanalytical Laboratory of the University Hospital in Pilsen examined sera from 263 patients being treated at the Hospital's Urology Department with suspected prostate cancer who had undergone biopsies and were divided into a benign and malignant group. The monitored biomarkers were measured using chemiluminescence. All statistical analyses were calculated using the SAS software. RESULTS: We found statistically significantly increased levels of -2proPSA, PHI and PSA and decreased levels of %freePSA in patients diagnosed with prostate cancer by prostate biopsy vs. patients with benign prostatic hypertrophy (median values: -2proPSA: 16 vs. 21 ng/l, PHI: 35 vs. 62, total PSA: 7.2 vs. 7.7 μg/l and %free PSA: 16.7 vs. 11.7%). Receiver operating characteristic curves showed the best performance for PHI compared to other markers. CONCLUSION: The assessment of -2proPSA and the calculation of PHI appear to be of great benefit for a more accurate differential diagnosis of benign hyperplasia and prostate cancer.
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- $a Fuchsova, Radka $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic fuchsovar@fnplzen.cz.
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- $a AIM: To evaluate changes in the serum levels of prostate specific antigen (PSA), %free PSA and -2proPSA biomarkers, and prostate health index (PHI) in the diagnostic algorithm of early prostate cancer. PATIENTS AND METHODS: The Immunoanalytical Laboratory of the University Hospital in Pilsen examined sera from 263 patients being treated at the Hospital's Urology Department with suspected prostate cancer who had undergone biopsies and were divided into a benign and malignant group. The monitored biomarkers were measured using chemiluminescence. All statistical analyses were calculated using the SAS software. RESULTS: We found statistically significantly increased levels of -2proPSA, PHI and PSA and decreased levels of %freePSA in patients diagnosed with prostate cancer by prostate biopsy vs. patients with benign prostatic hypertrophy (median values: -2proPSA: 16 vs. 21 ng/l, PHI: 35 vs. 62, total PSA: 7.2 vs. 7.7 μg/l and %free PSA: 16.7 vs. 11.7%). Receiver operating characteristic curves showed the best performance for PHI compared to other markers. CONCLUSION: The assessment of -2proPSA and the calculation of PHI appear to be of great benefit for a more accurate differential diagnosis of benign hyperplasia and prostate cancer.
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- $a Topolcan, Ondrej $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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- $a Pecen, Ladislav $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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- $a Kasik, Petr $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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- $a Novak, Jaroslav $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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- $a Smejkal, Jiri $u Department of Nuclear Medicine, Immunoanalytical Laboratory, University Hospital and Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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