Harris Health/Ben Taub Hospital, Baylor College of Medicine and Dan L. Duncan Comprehensive Cancer Center, Houston, TX
Michael Austin Brooks , Lewis Thomas , Cristina Magi-Galluzi , Jianbo Li , Michael Crager , Ruixiao Lu , John Abran , Tamer Aboushwareb , Eric A. Klein
Background: Adverse pathology (AP) at radical prostatectomy (RP) is often used as a proxy for long-term prostate cancer outcomes. The goal of this study was to assess the association of AP at RP, defined as high-grade (> Grade Group 3) and/or non-organ confined disease (pT3), with distant metastasis and prostate cancer death. Methods: A stratified cohort sample of 428 patients was used to evaluate the association of adverse pathology with the risk of distant metastases and prostate cancer-specific mortality over 20 years after prostatectomy in 2641 patients treated between 1987-2004. Cox regression of cause-specific hazards was used to estimate the absolute risk of both endpoints, with death from other causes treated as a competing risk. Subgroup analysis in patients with low/intermediate risk disease potentially eligible for active surveillance was performed. Results: Among the 428 patients, 343 had AUA Low or Intermediate risk disease and 85 had High risk disease. Median follow-up time was 15.5 years (IQR 14.6–16.6 years). Using the cohort sampling weights for estimation, at RP 29.8% of patients had high-grade disease, 42.3 % had non-organ confined disease, 19.3% had both, and thus 52.8% had AP. Adverse pathology was highly associated with metastasis and prostate cancer mortality in the overall cohort (HR 12.30, 95% CI 5.30-28.55, and 10.03, 95% CI 3.42-29.47, respectively, both p<0.001), and in the low/intermediate risk subgroup potentially eligible for active surveillance (HR 10.48, 95% CI 4.18-26.28, and 8.60, 95% CI 2.40-30.84, respectively, both p≤0.001). Conclusions: Adverse pathology at radical prostatectomy is highly associated with future development of metastasis and prostate cancer mortality and may be used as a short-term predictor of outcomes.
Event | 20-year absolutea risk of event (95% CI) | ||
---|---|---|---|
Hazard ratio (95% CI) for AP | Absence of AP | Presence of AP | |
All patients (n=428) | |||
Distant metastasis | 12.30 (5.30, 28.55) | 1.5% (0.7%, 3.5%) | 16.9% (13.2%, 21.4%) |
(105 events) | p<.001 | ||
Prostate cancer mortality | 10.03 (3.42, 29.47) | 0.6% (0.2%, 1.7%) | 5.8% (4.2%, 7.9%) |
(53 events) | p<.001 | ||
Low and Intermediate Risk patients (n = 343) | |||
Distant metastasis | 10.48 (4.18, 26.28) | 1.5% (0.6%, 3.6%) | 13.9% (10.2%, 18.9%) |
(67 events) | p<.001 | ||
Prostate cancer mortality | 8.60 (2.40, 30.84) | 0.5% (0.1%, 1.6%) | 4.0% (2.6%, 6.2%) |
(30 events) | p=.001 |
aAbsolute risk treating death due to non-prostate-cancer causes as a competing risk. AP=adverse pathology; CI = confidence interval
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