Affiliation:
1. Department of Urology Tokyo Medical University Tokyo Japan
2. Anatomic Pathology Tokyo Medical University Tokyo Japan
3. Department of Health Data Science Tokyo Medical University Tokyo Japan
Abstract
AbstractBackgroundIn prostate cancer, histological cribriform patterns are categorized as Gleason pattern 4, and recent studies have indicated that their size and percentage are associated with the risk of biochemical recurrence (BCR). However, these studies included a mixture of cases with various Gleason scores (GSs). We therefore examined the prognostic value of the area and percentage of cribriform patterns in patients with GS 4 + 4 prostate cancer.MethodsWe investigated 108 patients with GS 4 + 4 prostate cancer who underwent robot‐assisted radical prostatectomy (RARP). After digitally scanning the hematoxylin and eosin‐stained slides, we measured the area of the entire cancer and cribriform patterns. Predictive factors for BCR were explored using log‐rank test and Cox proportional hazard model analyses.ResultsSixty‐seven (62.0%) patients had a cribriform pattern in RARP specimens, and 32 (29.6%) experienced BCR. The median total cancer area, cribriform pattern area, and percentage of cribriform pattern area (% cribriform) were 427.70 mm2 (interquartile range [IQR], 171.65–688.53 mm2), 8.85 mm2 (IQR, 0–98.83 mm2), and 2.44% (IQR, 0%–33.70%), respectively. Univariate analyses showed that higher preoperative serum prostate‐specific antigen (PSA) levels, positive resection margins, advanced pathological T stage, extraprostatic extension, larger total cancer area, larger cribriform morphology area, and higher % cribriform values were significantly associated with BCR. A multivariate analysis demonstrated that the PSA level (hazard ratio [HR], 1.061; 95% confidence interval [CI], 1.011–1.113; p = 0.017) and % cribriform (HR, 1.018; 95% CI, 1.005–1.031; p = 0.005) were independent predictors of BCR.ConclusionsAn increased % cribriform value was associated with BCR in patients with GS 4 + 4 prostate cancer following RARP.
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