Review Article

Decision Support Systems in Prostate Cancer Treatment: An Overview

Table 1

Overview of diagnosis support systems.

StudyNDecision/DiagnoseInputsOutcomesTRIPOD

(Roach et al. 1994)[25]282Low or high risk of LN involvementPSA,GS, Clinical stageP LN involvement 79%

(Diaz et al. 1994)[26]217Low or high risk of SV involvementPSA, GSP SV involvement69%

(D’Amico et al. 1998)[27]1872Patient risk groupPSA, GS, Clinical stage5-year PSA outcome72%

(Chang et al. 1999)[28]43Localized vs Advanced PCaPSA, GS, TRUS, DREP advanced PCa and P localized PCa65%

(Roach et al. 2000)[29]895Extracapsular extensionPSA, GSExtracapsular extension risk92%

(Lee et al. 2010)[30]1077BiopsyClinical, Imaging, PSAP PCa86%

(Kim et al. 2011)[31]532Advanced PCaTRUS, Clinical, PSAP advanced PCa79%

(Shah et al. 2012)[32]31Location PCaMRI imageCancer probability map83%

(Mukai et al. 2013)[33]30773PSA testClinicalRecommendation-

(Sadoughi et al. 2014)[34]360PCaPSA, AgeP PCa33%

(van Leeuwen et al. 2017)[35]591Significant PCaClinical, PSA, PIRADS, DREP significant PCa97%

(Tosoian, et al. 2017)[36]4459Pathological StagePSA, GS, Clinical stage% likelihood of given stage83%

Abbreviations. N: number of patients; P: probability; PCa: prostate cancer; PSA: prostate specific antigen; PIRADS: Prostate Imaging Reporting and Data System; TRUS: transrectal ultrasound scan; LN: lymph node; GS: Gleason score; SV: seminal vesicles; TRIPOD: adherence to the TRIPOD statement; DRE: digital rectal examination.
Clinical, imaging, and tumor parameters.
Abstract only.
No development or validation of mDSS: no TRIPOD evaluation possible.