TY - JOUR
T1 - Differences in histopathological and biochemical outcomes in patients with low Gleason score prostate cancer
AU - Isbarn, Hendrik
AU - Karakiewicz, Pierre I.
AU - Ahyai, Sascha A.
AU - Chun, Felix K.H.
AU - Jeldres, Claudio
AU - Haese, Alexander
AU - Heinzer, Hans
AU - Zacharias, Mario
AU - Heuer, Roman
AU - Eichelberg, Christian
AU - Steuber, Thomas
AU - Budäus, Lars
AU - Köllermann, Jens
AU - Salomon, Georg
AU - Schlomm, Thorsten
AU - Perrotte, Paul
AU - Fisch, Margit
AU - Huland, Hartwig
AU - Graefen, Markus
PY - 2010/3
Y1 - 2010/3
N2 - Study Type - Diagnosis (case series) Level of Evidence 4 Objective: To test whether the number or percentage of positive biopsy cores can be used to discriminate between patients with prostate cancer of a favourable and less favourable Gleason score (GS) ≤3 + 3, as prognostically, not all GS 3 + 3 prostate cancers are the same. Patients and methods: In all, 1106 consecutive patients with a prostate-specific antigen (PSA) level of ≤10 ng/mL and a biopsy GS of ≤3 + 3 or 3 + 4 had an open radical prostatectomy. The number of positive biopsy cores (≤2 vs ≥3) were stratified into low- vs high-risk groups. Subsequently, we stratified patients according to the GS and the percentage of positive biopsy cores (<50% vs ≥50%). The pathological stage and the 5-year biochemical recurrence (BCR)-free survival rates were examined in univariable and multivariable models. Results: Based on the number of positive cores, the rate of extraprostatic disease was 11.7% and 23.3%, respectively, in the low-and high-risk GS ≤3 + 3 groups (P < 0.001). The 5-year BCR-free survival rates were 95.0%, 77.8%, 81.2% and 66.5% for, respectively, low- and high-risk GS ≤3 + 3 and for low- and high-risk GS 3 + 4 patients. Univariable and multivariable intergroup BCR rate differences were statistically significant between low- vs high-risk GS 3 + 3 patients (P < 0.001), but not significant between high-risk GS ≤3 + 3 vs low-risk GS 3 + 4 patients (P = 0.6). Comparable results were obtained when comparisons were made according to the percentage of positive biopsy cores. Conclusion:S Our results corroborate the finding that not all patients with a biopsy GS of ≤3 + 3 prostate cancer have low-risk disease. High-risk GS ≤3 + 3 patients have a similar risk profile as more favourable GS 3 + 4 patients. This finding warrants consideration when deciding on treatment.
AB - Study Type - Diagnosis (case series) Level of Evidence 4 Objective: To test whether the number or percentage of positive biopsy cores can be used to discriminate between patients with prostate cancer of a favourable and less favourable Gleason score (GS) ≤3 + 3, as prognostically, not all GS 3 + 3 prostate cancers are the same. Patients and methods: In all, 1106 consecutive patients with a prostate-specific antigen (PSA) level of ≤10 ng/mL and a biopsy GS of ≤3 + 3 or 3 + 4 had an open radical prostatectomy. The number of positive biopsy cores (≤2 vs ≥3) were stratified into low- vs high-risk groups. Subsequently, we stratified patients according to the GS and the percentage of positive biopsy cores (<50% vs ≥50%). The pathological stage and the 5-year biochemical recurrence (BCR)-free survival rates were examined in univariable and multivariable models. Results: Based on the number of positive cores, the rate of extraprostatic disease was 11.7% and 23.3%, respectively, in the low-and high-risk GS ≤3 + 3 groups (P < 0.001). The 5-year BCR-free survival rates were 95.0%, 77.8%, 81.2% and 66.5% for, respectively, low- and high-risk GS ≤3 + 3 and for low- and high-risk GS 3 + 4 patients. Univariable and multivariable intergroup BCR rate differences were statistically significant between low- vs high-risk GS 3 + 3 patients (P < 0.001), but not significant between high-risk GS ≤3 + 3 vs low-risk GS 3 + 4 patients (P = 0.6). Comparable results were obtained when comparisons were made according to the percentage of positive biopsy cores. Conclusion:S Our results corroborate the finding that not all patients with a biopsy GS of ≤3 + 3 prostate cancer have low-risk disease. High-risk GS ≤3 + 3 patients have a similar risk profile as more favourable GS 3 + 4 patients. This finding warrants consideration when deciding on treatment.
KW - Biochemical recurrence
KW - Gleason score
KW - Indolent
KW - Prostate cancer
KW - Radical prostatectomy
UR - https://www.scopus.com/pages/publications/77649241814
UR - https://www.scopus.com/inward/citedby.url?scp=77649241814&partnerID=8YFLogxK
U2 - 10.1111/j.1464-410X.2009.08841.x
DO - 10.1111/j.1464-410X.2009.08841.x
M3 - Article
C2 - 19751264
AN - SCOPUS:77649241814
SN - 1464-4096
VL - 105
SP - 818
EP - 823
JO - BJU International
JF - BJU International
IS - 6
ER -