Upgrading of Gleason score and prostate volume: A clinicopathological analysis - Abstract

OBJECTIVE: To more clearly elucidate the association between prostate volume and Gleason score (GS) upgrading.

PATIENT AND METHODS: We reviewed 451 patients with prostate cancer with a GS of 6 on biopsy, who underwent radical prostatectomy without neoadjuvant treatment. As a preoperative variable, we assessed the independent effect of prostate volume on GS upgrading. To evaluate the association between prostate volume and GS upgrading, we developed multivariate models with volumetric pathological variables, including postoperative tumour volume and percent tumour volume (tumour volume as a percentage of prostate volume).

RESULTS: GS upgrading was observed in 194 patients (43.0%). As a preoperative variable, smaller prostate volume was an independent predictor of GS upgrading. In regression analysis, prostate volume and postoperative tumour volume were inversely correlated. On multivariate analysis including volumetric pathological variables, tumour volume was a strong independent factor influencing GS upgrading, and prostate volume lost statistical significance after adjusting for tumour volume. Percent tumour volume was inversely correlated with GS upgrading after adjusting for tumour volume.

CONCLUSIONS: Smaller prostate volume was an independent predictor of GS upgrading as a preoperative variable. The inverse relationship between prostate volume and GS upgrading seems to be attributable to cancer biology, which was represented by tumour volume in our study. Percent tumour volume was also inversely associated with GS upgrading. These results suggest that biological factors and sampling error both play important roles in GS upgrading.

Written by:
Kim KH, Lim SK, Shin TY, Lee JY, Chung BH, Rha KH, Hong SJ.   Are you the author?
Department of Urology, Urological Science Institute, Yonsei University College of Medicine, Seoul, Korea.

Reference: BJU Int. 2013 Mar 4. Epub ahead of print.
doi: 10.1111/j.1464-410X.2013.11799.x


PubMed Abstract
PMID: 23452115

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