TY - JOUR
T1 - Assessment of PSIM (Prostatic Systemic Inflammatory Markers) Score in Predicting Pathologic Features at Robotic Radical Prostatectomy in Patients with Low-Risk Prostate Cancer Who Met the Inclusion Criteria for Active Surveillance
AU - Ferro, Matteo
AU - Musi, Gennaro
AU - Matei, Deliu Victor
AU - Mistretta, Alessandro Francesco
AU - Luzzago, Stefano
AU - Cozzi, Gabriele
AU - Bianchi, Roberto
AU - Di Trapani, Ettore
AU - Cioffi, Antonio
AU - Lucarelli, Giuseppe
AU - Busetto, Gian Maria
AU - Del Giudice, Francesco
AU - Russo, Giorgio Ivan
AU - Di Mauro, Marina
AU - Porreca, Angelo
AU - Renne, Giuseppe
AU - Catellani, Michele
AU - Bottero, Danilo
AU - Brescia, Antonio
AU - Cordima, Giovanni
AU - de Cobelli, Ottavio
PY - 2021/2/20
Y1 - 2021/2/20
N2 - BACKGROUND: circulating levels of lymphocytes, platelets and neutrophils have been identified as factors related to unfavorable clinical outcome for many solid tumors. The aim of this cohort study is to evaluate and validate the use of the Prostatic Systemic Inflammatory Markers (PSIM) score in predicting and improving the detection of clinically significant prostate cancer (csPCa) in men undergoing robotic radical prostatectomy for low-risk prostate cancer who met the inclusion criteria for active surveillance.METHODS: we reviewed the medical records of 260 patients who fulfilled the inclusion criteria for active surveillance. We performed a head-to-head comparison between the histological findings of specimens after radical prostatectomy (RP) and prostate biopsies. The PSIM score was calculated on the basis of positivity according to cutoffs (neutrophil-to-lymphocyte ratio (NLR) 2.0, platelets-to-lymphocyte ratio (PLR) 118 and monocyte-to-lymphocyte-ratio (MLR) 5.0), with 1 point assigned for each value exceeding the specified threshold and then summed, yielding a final score ranging from 0 to 3.RESULTS: median NLR was 2.07, median PLR was 114.83, median MLR was 3.69.CONCLUSION: we found a significantly increase in the rate of pathological International Society of Urological Pathology (ISUP) ≥ 2 with the increase of PSIM. At the multivariate logistic regression analysis adjusted for age, prostate specific antigen (PSA), PSA density, prostate volume and PSIM, the latter was found the sole independent prognostic variable influencing probability of adverse pathology.
AB - BACKGROUND: circulating levels of lymphocytes, platelets and neutrophils have been identified as factors related to unfavorable clinical outcome for many solid tumors. The aim of this cohort study is to evaluate and validate the use of the Prostatic Systemic Inflammatory Markers (PSIM) score in predicting and improving the detection of clinically significant prostate cancer (csPCa) in men undergoing robotic radical prostatectomy for low-risk prostate cancer who met the inclusion criteria for active surveillance.METHODS: we reviewed the medical records of 260 patients who fulfilled the inclusion criteria for active surveillance. We performed a head-to-head comparison between the histological findings of specimens after radical prostatectomy (RP) and prostate biopsies. The PSIM score was calculated on the basis of positivity according to cutoffs (neutrophil-to-lymphocyte ratio (NLR) 2.0, platelets-to-lymphocyte ratio (PLR) 118 and monocyte-to-lymphocyte-ratio (MLR) 5.0), with 1 point assigned for each value exceeding the specified threshold and then summed, yielding a final score ranging from 0 to 3.RESULTS: median NLR was 2.07, median PLR was 114.83, median MLR was 3.69.CONCLUSION: we found a significantly increase in the rate of pathological International Society of Urological Pathology (ISUP) ≥ 2 with the increase of PSIM. At the multivariate logistic regression analysis adjusted for age, prostate specific antigen (PSA), PSA density, prostate volume and PSIM, the latter was found the sole independent prognostic variable influencing probability of adverse pathology.
U2 - 10.3390/diagnostics11020355
DO - 10.3390/diagnostics11020355
M3 - Article
SN - 2075-4418
VL - 11
SP - 1
EP - 9
JO - Diagn.
JF - Diagn.
IS - 2
M1 - 355
ER -