Your browser doesn't support javascript.
loading
Integrating inflammatory serum biomarkers into a risk calculator for prostate cancer detection.
Jalali, Amirhossein; Kitching, Michael; Martin, Kenneth; Richardson, Ciaran; Murphy, Thomas Brendan; FitzGerald, Stephen Peter; Watson, Ronald William; Perry, Antoinette Sabrina.
Afiliación
  • Jalali A; UCD Conway Institute of Biomedical and Biomolecular Science, Dublin, Ireland. amir.jalali@ucc.ie.
  • Kitching M; UCD School of Medicine, University College Dublin, Dublin, Ireland. amir.jalali@ucc.ie.
  • Martin K; School of Mathematical Sciences, University College Cork, Cork, Ireland. amir.jalali@ucc.ie.
  • Richardson C; UCD Conway Institute of Biomedical and Biomolecular Science, Dublin, Ireland.
  • Murphy TB; UCD School of Biology and Environmental Science, University College Dublin, Dublin, Ireland.
  • FitzGerald SP; Randox Teoranta, Co, Donegal, Ireland.
  • Watson RW; Randox Teoranta, Co, Donegal, Ireland.
  • Perry AS; School of Mathematics and Statistics, University College Dublin, Dublin, Ireland.
Sci Rep ; 11(1): 2525, 2021 01 28.
Article en En | MEDLINE | ID: mdl-33510263
ABSTRACT
Improved prostate cancer detection methods would avoid over-diagnosis of clinically indolent disease informing appropriate treatment decisions. The aims of this study were to investigate the role of a panel of Inflammation biomarkers to inform the need for a biopsy to diagnose prostate cancer. Peripheral blood serum obtained from 436 men undergoing transrectal ultrasound guided biopsy were assessed for a panel of 18 inflammatory serum biomarkers in addition to Total and Free Prostate Specific Antigen (PSA). This panel was integrated into a previously developed Irish clinical risk calculator (IPRC) for the detection of prostate cancer and high-grade prostate cancer (Gleason Score ≥ 7). Using logistic regression and multinomial regression methods, two models (Logst-RC and Multi-RC) were developed considering linear and nonlinear effects of the panel in conjunction with clinical and demographic parameters for determination of the two endpoints. Both models significantly improved the predictive ability of the clinical model for detection of prostate cancer (from 0.656 to 0.731 for Logst-RC and 0.713 for Multi-RC) and high-grade prostate cancer (from 0.716 to 0.785 for Logst-RC and 0.767 for Multi-RC) and demonstrated higher clinical net benefit. This improved discriminatory power and clinical utility may allow for individualised risk stratification improving clinical decision making.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Biomarcadores / Mediadores de Inflamación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article País de afiliación: Irlanda

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Biomarcadores / Mediadores de Inflamación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Año: 2021 Tipo del documento: Article País de afiliación: Irlanda