Are biochemical recurrence outcomes similar after radical prostatectomy and radiation therapy? Analysis of prostate cancer-specific mortality by nomogram-predicted risks of biochemical recurrence
- PMID: 25294696
- DOI: 10.1016/j.eururo.2014.09.017
Are biochemical recurrence outcomes similar after radical prostatectomy and radiation therapy? Analysis of prostate cancer-specific mortality by nomogram-predicted risks of biochemical recurrence
Abstract
Background: Due to the protracted natural history of the clinical progression of prostate cancer, biochemical recurrence (BCR) is often used to compare treatment modalities. However, BCR definitions and posttreatment prostate-specific antigen kinetics vary considerably among treatments, calling into the question the validity of such comparisons.
Objective: To analyze prostate cancer-specific mortality (PCSM) according to treatment-specific nomogram-predicted risk of BCR for men treated by radical prostatectomy (RP), external-beam radiation therapy (EBRT), and brachytherapy.
Design, setting, and participants: A total of 13 803 men who underwent RP, EBRT, or brachytherapy at two US high-volume hospitals between 1995 and 2008.
Intervention: RP, EBRT, and brachytherapy.
Outcome measurements and statistical analysis: The 5-yr progression-free probability (5Y-PFP) was calculated for each patient based on the treatment received using a validated treatment-specific nomogram. Fine and Gray competing risk analysis was then used to estimate PCSM by a patient's predicted 5Y-PFP. Multivariable competing risk regression analysis was used to determine the association of treatment with PCSM after adjusting for nomogram-predicted 5Y-PFP.
Results and limitations: Men receiving EBRT had higher 10-yr PCSM compared with those treated by RP across the range of nomogram-predicted risks of BCR: 5Y-PFP >75%, 3% versus 0.9%; 5Y-PFP 51-75%, 6.8% versus 5.9%; 5Y-PFP 26-50%, 12.2% versus 10.6%; and 5Y-PFP ≤25%, 26.6% versus 21.2%. After adjusting for nomogram-predicted 5Y-PFP, EBRT was associated with a significantly increased PCSM risk compared with RP (hazard ratio: 1.5; 95% confidence interval, 1.1-2.0; p=0.006). No statistically significant difference in PCSM was observed between patients treated by brachytherapy and RP, although patient selection factors and lack of statistical power limited this analysis.
Conclusions: EBRT patients with similar nomogram-predicted 5Y-PFP appear to have a significantly increased risk of PCSM compared with those treated by RP. Comparison of treatments using nomogram-predicted BCR end points may not be valid.
Patient summary: Biochemical recurrence (BCR) outcomes after external-beam radiation therapy and radical prostatectomy are associated with different risks of subsequent prostate cancer-specific mortality. Physicians and patients should cautiously interpret BCR end points when comparing treatments to make treatment decisions.
Keywords: Brachytherapy; Comparative effectiveness research; Models; Mortality; Nomograms; Observational study; Prospective studies; Prostatectomy; Prostatic neoplasms; Radiotherapy; Statistical; Survival.
Copyright © 2014. Published by Elsevier B.V.
Comment in
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Prostate cancer: treatment-specific nomograms, biochemical recurrence, and prostate cancer-specific mortality.Nat Rev Urol. 2014 Dec;11(12):657. doi: 10.1038/nrurol.2014.294. Epub 2014 Oct 21. Nat Rev Urol. 2014. PMID: 25330792 No abstract available.
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Radical prostatectomy versus radiation therapy: can pretreatment nomograms be used to select the appropriate prostate cancer treatment?Eur Urol. 2015 Feb;67(2):210-1. doi: 10.1016/j.eururo.2014.10.009. Epub 2014 Oct 28. Eur Urol. 2015. PMID: 25457494 No abstract available.
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Re: Byron H. Lee, Adam S. Kibel, Jay P. Ciezki, et al. Are biochemical recurrence outcomes similar after radical prostatectomy and radiation therapy? Analysis of prostate cancer-specific mortality by nomogram-predicted risks of biochemical recurrence. Eur Urol 2015;67:204-9.Eur Urol. 2015 Sep;68(3):e61-2. doi: 10.1016/j.eururo.2015.04.015. Epub 2015 Apr 22. Eur Urol. 2015. PMID: 25913064 No abstract available.
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