TY - JOUR
T1 - The effect of differing gleason scores at biopsy on the odds of upgrading and the risk of death from prostate cancer
AU - Phillips, John G.
AU - Aizer, Ayal A.
AU - Chen, Ming Hui
AU - Zhang, Danjie
AU - Hirsch, Michelle S.
AU - Richie, Jerome P.
AU - Tempany, Clare M.
AU - Williams, Stephen
AU - Hegde, John V.
AU - Loffredo, Marian J.
AU - D'Amico, Anthony V.
N1 - Funding Information:
This work was supported by NIH grants: EB 015898 and CA 111288.
Publisher Copyright:
© 2014 Elsevier Inc. All rights reserved.
PY - 2014
Y1 - 2014
N2 - We provide evidence that differing Gleason scores (GSs) at biopsy (ComboGS) is associated with an approximately 80% decrease in the odds of upgrading and a 60% decrease in the risk of prostate cancer-specific mortality (PCSM) after definitive treatment. If validated, future randomized noninferiority studies evaluating deescalated treatment approaches in men with ComboGS could be considered. Introduction/Background: The GS is an established prostate cancer prognostic factor. Whether the presence of differing GSs at biopsy (eg, 4+3 and 3+3), which we term ComboGS, improves the prognosis that would be predicted based on the highest GS (eg, 4+3) because of decreased upgrading is unknown. Therefore, we evaluated the odds of upgrading at time of radical prostatectomy (RP) and the risk of PCSM when ComboGS was present versus absent. Patients and Methods: Logistic and competing risks regression were performed to assess the effect that ComboGS had on the odds of upgrading at time of RP in the index (n = 134) and validation cohorts (n = 356) and the risk of PCSM after definitive therapy in a long-term cohort (n = 666), adjusting for known predictors of these end points. We calculated and compared the area under the curve using a receiver operating characteristic analysis when ComboGS was included versus excluded from the upgrading models. Results: ComboGS was associated with decreased odds of upgrading (index: adjusted odds ratio [AOR], 0.14; 95% confidence interval [CI], 0.04-0.50; P = .003; validation: AOR, 0.24; 95% CI, 0.11-0.51; P < .001) and added significantly to the predictive value of upgrading for the in-sample index (P = .02), validation (P = .003), and out-of-sample prediction models (P = .002). ComboGS was also associated with a decreased risk of PCSM (adjusted hazard ratio, 0.40; 95% CI, 0.19-0.85; P = .02). Conclusion: Differing biopsy GSs are associated with a lower odds of upgrading and risk of PCSM. If validated, future randomized noninferiority studies evaluating deescalated treatment approaches in men with ComboGS could be considered.
AB - We provide evidence that differing Gleason scores (GSs) at biopsy (ComboGS) is associated with an approximately 80% decrease in the odds of upgrading and a 60% decrease in the risk of prostate cancer-specific mortality (PCSM) after definitive treatment. If validated, future randomized noninferiority studies evaluating deescalated treatment approaches in men with ComboGS could be considered. Introduction/Background: The GS is an established prostate cancer prognostic factor. Whether the presence of differing GSs at biopsy (eg, 4+3 and 3+3), which we term ComboGS, improves the prognosis that would be predicted based on the highest GS (eg, 4+3) because of decreased upgrading is unknown. Therefore, we evaluated the odds of upgrading at time of radical prostatectomy (RP) and the risk of PCSM when ComboGS was present versus absent. Patients and Methods: Logistic and competing risks regression were performed to assess the effect that ComboGS had on the odds of upgrading at time of RP in the index (n = 134) and validation cohorts (n = 356) and the risk of PCSM after definitive therapy in a long-term cohort (n = 666), adjusting for known predictors of these end points. We calculated and compared the area under the curve using a receiver operating characteristic analysis when ComboGS was included versus excluded from the upgrading models. Results: ComboGS was associated with decreased odds of upgrading (index: adjusted odds ratio [AOR], 0.14; 95% confidence interval [CI], 0.04-0.50; P = .003; validation: AOR, 0.24; 95% CI, 0.11-0.51; P < .001) and added significantly to the predictive value of upgrading for the in-sample index (P = .02), validation (P = .003), and out-of-sample prediction models (P = .002). ComboGS was also associated with a decreased risk of PCSM (adjusted hazard ratio, 0.40; 95% CI, 0.19-0.85; P = .02). Conclusion: Differing biopsy GSs are associated with a lower odds of upgrading and risk of PCSM. If validated, future randomized noninferiority studies evaluating deescalated treatment approaches in men with ComboGS could be considered.
KW - ComboGS
KW - Pathology
KW - Prognostic factors
KW - Prostate cancer-specific mortality
KW - Radical prostatectomy
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U2 - 10.1016/j.clgc.2014.02.008
DO - 10.1016/j.clgc.2014.02.008
M3 - Article
C2 - 24721618
AN - SCOPUS:84922658718
SN - 1558-7673
VL - 12
SP - e181-e187
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 5
ER -