Literature DB >> 20018437

Head-to-head comparison of the three most commonly used preoperative models for prediction of biochemical recurrence after radical prostatectomy.

Giovanni Lughezzani1, Lars Budäus, Hendrik Isbarn, Maxine Sun, Paul Perrotte, Alexander Haese, Felix K Chun, Thorsten Schlomm, Thomas Steuber, Hans Heinzer, Hartwig Huland, Francesco Montorsi, Markus Graefen, Pierre I Karakiewicz.   

Abstract

BACKGROUND: Several models can predict the rate of biochemical recurrence (BCR) after radical prostatectomy (RP).
OBJECTIVE: We tested the three most commonly used models-the D'Amico risk stratification scheme, the Cancer of the Prostate Risk Assessment (CAPRA) score, and the Stephenson nomogram-in a European cohort of RP patients. DESIGN, SETTING, AND PARTICIPANTS: We relied on preoperative characteristics and prostate-specific antigen follow-up data of 1976 patients, as required by the three tested models. All patients were treated with an open RP between 1992 and 2006. MEASUREMENTS: Analyses included tests of accuracy (Harrell's concordance index) and calibration between predicted and observed BCR rates at 3 yr and 5 yr after RP. Additionally, we relied on decision curve analyses to compare the three models directly in a head-to-head fashion. RESULTS AND LIMITATIONS: The median follow-up of censored patients was 32 mo. BCR-free rates at 3 yr and 5 yr after RP were 80.2% and 72.6%, respectively. The concordance index for 3-yr BCR predictions was 70.4%, 74.3%, and 75.2% for the D'Amico, CAPRA, and Stephenson models, respectively, versus 67.4%, 72.9%, and 73.5% for 5-yr BCR predictions. Calibration results supported the use of either the CAPRA or Stephenson models. Decision curve analyses indicated a small benefit for the CAPRA score relative to the Stephenson nomogram. Our findings apply to German patients treated with RP at a high-volume tertiary care centre. Consequently, the rank order reported in this paper may not be the same in North American or other European cohorts.
CONCLUSIONS: Different methods yield different results, and it may be difficult to reconcile concordance index, calibration, and decision curve analysis findings. Our data suggest that the CAPRA score outperforms the other models when decision curve analysis and calibration were used as benchmarks. Conversely, the Stephenson nomogram outperformed the other models when concordance index was used as a metric. Crown
Copyright © 2009. Published by Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 20018437     DOI: 10.1016/j.eururo.2009.12.003

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  26 in total

1.  Use of tumor dynamics to clarify the observed variability among biochemical recurrence nomograms for prostate cancer.

Authors:  Guy Dimonte; E J Bergstralh; M E Bolander; R J Karnes; D J Tindall
Journal:  Prostate       Date:  2011-05-31       Impact factor: 4.104

Review 2.  Predictive and prognostic models in radical prostatectomy candidates: a critical analysis of the literature.

Authors:  Giovanni Lughezzani; Alberto Briganti; Pierre I Karakiewicz; Michael W Kattan; Francesco Montorsi; Shahrokh F Shariat; Andrew J Vickers
Journal:  Eur Urol       Date:  2010-08-06       Impact factor: 20.096

3.  The CAPRA-S score: A straightforward tool for improved prediction of outcomes after radical prostatectomy.

Authors:  Matthew R Cooperberg; Joan F Hilton; Peter R Carroll
Journal:  Cancer       Date:  2011-06-03       Impact factor: 6.860

4.  Preoperative sex steroids are significant predictors of early biochemical recurrence after radical prostatectomy.

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7.  Positive STAT5 Protein and Locus Amplification Status Predicts Recurrence after Radical Prostatectomy to Assist Clinical Precision Management of Prostate Cancer.

Authors:  Bassem R Haddad; Andrew Erickson; Vindhya Udhane; Peter S LaViolette; Janice D Rone; Markku A Kallajoki; William A See; Antti Rannikko; Tuomas Mirtti; Marja T Nevalainen
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Review 8.  Risk stratification of prostate cancer: integrating multiparametric MRI, nomograms and biomarkers.

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10.  [Postoperative radiation therapy for prostate cancer : Still no genomic risk profiling for clinical routine].

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