Risk of death from prostate cancer after radical prostatectomy or brachytherapy in men with low- or intermediate-risk disease.

Authors

null

Nils Arvold

Harvard Radiation Oncology Program

Nils Arvold , Judd Moul , Brian Moran , Daniel Dosoretz , Lionel Banez , Michael Katin , Anthony D'Amico

Organizations

Harvard Radiation Oncology Program, Duke University Medical Center, Prostate Cancer Foundation of Chicago, 21st Century Oncology, Dana-Farber Cancer Institute/Brigham and Women's Hospital

Research Funding

No funding sources reported

Background: Radical prostatectomy (RP) and brachytherapy (BT) are widely utilized treatments for favorable-risk prostate cancer (PC). We estimated the risk of PC-specific mortality (PCSM) following RP or BT in men with low- or intermediate-risk PC using prospectively collected data. Methods: The study cohort comprised 5,760 men with low-risk PC (prostate-specific antigen [PSA] level ≤ 10 ng/mL, clinical category T1c or 2a, and Gleason score ≤ 6), and 3,079 men with intermediate-risk PC (PSA level 10-20 ng/mL, clinical T2b or T2c, or Gleason score 7). Competing risks multivariable regression was performed to assess risk of PCSM after RP or BT, adjusting for age, treatment year, cardiovascular comorbidity, and known PC prognostic factors. Results: There was no significant difference in the risk of PCSM among men with low-risk PC (11 vs. 6 deaths: adjusted hazard ratio [AHR], 1.62; 95% CI, 0.59-4.45; P = 0.35) who received BT compared to RP. However among men with intermediate-risk PC, despite significantly shorter median follow-up for men undergoing BT as compared to RP (4.1 vs. 7.2 years, P < 0.001), there was a trend toward an increased risk of PCSM (18 vs. 9 deaths: AHR, 2.30; 95% CI, 0.95-5.58; P = 0.07) for men treated with BT. Conclusions: The risk of PCSM among men with low-risk PC was not significantly different following RP or BT, however there may be a reduced risk of PCSM after RP as compared to BT in men with intermediate-risk PC.
 



Risk of PCSM according to treatment type

PC risk groupRadical
prostatectomy
Brachytherapy

Low risk No. of men
No. of events
Multivariate AHR* (95% CI)
p value
1,909
6
1 [Reference]
-
3,851
11
1.62 (0.59-4.45)
.35
Intermediate risk No. of men
No. of events
Multivariate AHR (95% CI)
p value
1,028
9
1 [Reference]
-
2,051
18
2.30 (0.95-5.58)
.07

Abbreviations: PCSM, prostate cancer-specific mortality; PC, prostate cancer; AHR, adjusted hazard ratio. *AHR adjusted for treatment type, age, prostate-specific antigen level, Gleason score, clinical T category, and cardiovascular comorbidity. Among men with intermediate-risk PC, there was also an increased risk of PCSM with increasing age at treatment, per year increase (AHR, 1.05; 95% CI, 1.01-1.10; p = 0.03).

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Abstract Details

Meeting

2011 Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

General Poster Session B: Prostate Cancer

Track

Prostate Cancer

Sub Track

Prostate Cancer

Citation

J Clin Oncol 29: 2011 (suppl 7; abstr 198)

Abstract #

198

Poster Bd #

A92

Abstract Disclosures