Abstract
Background: There is no consensus on the optimal treatment for localized high-risk prostate cancer (PC), and much debate exists regarding the ideal treatment approach. For these reasons, we evaluated the competing risks of PC-specific mortality after initial therapy with radical prostatectomy (RP) versus radiotherapy (RT) in men with clinically localized high-risk PC.
Methods: We reviewed patients treated with RP and RT combined with androgen-deprivation therapy between 1990 and 2009. High-risk PC is defined as clinical stage ≥T3a, serum prostate-specific antigen (PSA) >20 ng/mL, or a biopsy Gleason sum of 8–10 according to National Comprehensive Cancer Network guidelines. Competing risk analysis was conducted to assess the association of RP (n = 251) or RT (n = 125) with cancer-specific mortality (CSM). Thereafter, secondary analysis with propensity score matching was conducted to further elucidate patient characteristics, with optimal matching of 0.25 times the standard deviation of propensity scores.
Results: With an overall median follow-up of 76 months, 35 (9.3 %) men with high-risk PC died due to PC (23 in the RT group and 12 in the RP group). The 5-year estimates of cancer-specific survival rate for men treated with RP and RT were 96.5 % (95 % confidence interval [CI] 94.2–98.9) and 88.3 % (95 % CI 82.8–94.3), respectively. Cumulative incidence estimates for CSM were statistically increased amongst men treated with RT (p = 0.002). Propensity score matching extracted 168 men with high-risk PC from the total patient cohort. Cumulative incidence estimates for CSM were statistically different amongst men treated with RT (p < 0.001).
Conclusions: Initial treatment with RP versus RT was associated with a decreased risk of CSM in men with clinically localized high-risk PC.
Original language | English |
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Pages (from-to) | 4026-4033 |
Number of pages | 8 |
Journal | Annals of surgical oncology |
Volume | 21 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2014 Oct 8 |
Bibliographical note
Funding Information:ACKNOWLEDGMENT This study was supported by a grant from the Korean Foundation for Cancer Research (CB-2011-04-02), Republic of Korea.
Publisher Copyright:
© 2014, Society of Surgical Oncology.
All Science Journal Classification (ASJC) codes
- Surgery
- Oncology