Abstract
Objective
We intended to analyze the outcomes and predictive factors for underestimating the
prostate cancer (PCa) grade group (GG) from prostate biopsies in a large monocentric
cohort of patients treated by minimally invasive radical prostatectomy (RP).
Materials and Methods
Using a monocentric prospectively maintained database, we included 3062 patients who
underwent minimally invasive RP between 2006 and 2013. We explored clinicopathologic
features and outcomes associated with a GG upgrade from biopsy to RP. Multivariate
logistic regression was used to develop and validate a nomogram to predict upgrading
for GG1.
Results
Biopsy GG was upgraded after RP in 51.5% of cases. Patients upgraded from GG1 to GG2
or GG3 after RP had a longer time to biochemical recurrence than those with GG2 or
GG3 respectively, on both biopsy and RP, but a shorter time to biochemical recurrence
than those who remained GG1 after RP (P < .0001). In multivariate analyses, variables predicting upgrading for GG1 PCa were
age (P = .0014), abnormal digital rectal examination (P < .0001), prostate-specific antigen density (P < .0001), percentage of positive cores (P < .0001), and body mass index (P = .037). A nomogram was generated and validated internally.
Conclusions
Biopsy grading system is misleading in approximately 50% of cases. Upgrading GG from
biopsy to RP may have consequences on clinical outcomes. A nomogram using clinicopathologic
features could aid the probability of needing to upgrade GG1 patients at their initial
evaluation.
Keywords
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Article info
Publication history
Published online: April 25, 2017
Accepted:
April 14,
2017
Received in revised form:
April 4,
2017
Received:
January 9,
2017
Identification
Copyright
© 2017 Elsevier Inc. All rights reserved.