Impact of preoperative risk on metastatic progression and cancer-specific mortality in patients with adverse pathology at radical prostatectomy

被引:6
|
作者
Boehm, Katharina [1 ,2 ]
Leyh-Bannurah, Sami-Ramzi [1 ,3 ]
Rosenbaum, Clemens
Brandi, Laurenz S. [1 ]
Budaeus, Lars [1 ]
Graefen, Markus [1 ]
Huland, Hartwig [1 ]
Haferkamp, Axel [2 ]
Tilki, Derya [1 ,3 ]
机构
[1] Univ Hosp Hamburg Eppendorf, Prostate Canc Ctr, Martini Klin, Hamburg, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Urol, Mainz, Germany
[3] Univ Hosp Hamburg Eppendorf, Dept Urol, Hamburg, Germany
关键词
prostate cancer; cancer-specific survival; low-risk; pathology; ACTIVE SURVEILLANCE; PROSTATIC ADENOCARCINOMA; MEN; VALIDATION; PREDICTION; MANAGEMENT; OUTCOMES;
D O I
10.1111/bju.13887
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveTo evaluate the impact of preoperative risk category on metastatic disease and prostate cancer-specific mortality (CSM) in patients with prostate cancer (PCa) with adverse pathology at radical prostatectomy (RP). Patients and MethodsThe records of 6 943 patients who underwent RP at a European tertiary centre were analysed. Biochemical recurrence (BCR), metastatic disease and CSM were assessed for patients with adverse pathology at RP, and stratified according to preoperative low- vs intermediate-/high-risk PCa groups. Kaplan-Meier, cumulative incidence, Cox regression and competing risk regression analyses were performed. ResultsIn patients with extracapsular extension, the metastatic disease rate was 1.6% vs 8% (P < 0.001) and the CSM rate was 2% vs 5% (P = 0.041) for low vs intermediate-/high-risk patients, respectively, at 10 years. In patients with pathological Gleason score 3+4, the metastatic disease rate was 3.0% vs 12% (P < 0.001) and the CSM rate was 3% vs 8%, respectively (P < 0.001). In patients with positive surgical margins (PSMs), the metastatic disease rate was 2.9% vs 15% (P < 0.001) and the CSM rate was 4% vs 10%, respectively (P = 0.0001). Low-risk status was a predictive factor for metastatic disease in patients with pathological Gleason score 3+4 (hazard ratio [HR] 0.51), pathological Gleason score 4+3 (HR 0.41) and PSMs (HR 0.46) and was a predictive factor for CSM risk in patients with pathological Gleason score 3+4 (HR 0.62). ConclusionsPatients with low-risk PCa were at significantly lower risk of metastatic disease and CSM than their intermediate-/high-risk counterparts, when adverse pathological features were identified at RP. This should be emphasized in the decision-making process after RP.
引用
收藏
页码:666 / 672
页数:7
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