Abstract
Simple SummaryThe current prostate cancer guidelines recommend performing the first prostate-specific antigen measurement at three months after radical prostatectomy. However, at an earlier measurement, persistence (≥0.1 ng/mL) of this biomarker could be found in up to 30% of cases, depending on the prostate cancer risk factors. Recent reports have demonstrated an increasing interest in prostate-specific antigen persistence as a possible additional predictor of disease progression and cancer-specific survival. However, the data remain scant, with weak evidence. We assessed the relationship between prostate-specific antigen persistence and long-term oncological outcomes within prostate cancer risk groups. We found that persistence of this biomarker could be used as an independent predictor of worse long-term outcomes in high-risk prostate cancer patients, while in intermediate-risk patients, this parameter significantly predicts only biochemical recurrence and has no impact on the outcomes in low-risk patients.Objective: To assess the significance of prostate-specific antigen (PSA) persistence at the first measurement after radical prostatectomy (RP) on long-term outcomes in different prostate cancer risk groups. Methods: Persistent PSA was defined as ≥0.1 ng/mL at 4–8 weeks after RP. Patients were stratified into low-, intermediate- and high-risk groups, according to the preoperative PSA, pathological stage, grade group and lymph nodes status. The ten-year cumulative incidence of biochemical recurrence (BCR), metastases, cancer-specific mortality (CSM) and overall mortality (OM) were calculated in patients with undetectable and persistent PSA in different PCa-risk groups. Multivariate regression analyses depicted the significance of PSA persistence on each study endpoint. Results: Of all 1225 men, in 246 (20.1%), PSA persistence was detected. These men had an increased risk of BCR (hazard ratio (HR) 4.2, p < 0.0001), metastases (HR: 2.7, p = 0.002), CRM (HR: 5.5, p = 0.002) and OM (HR: 1.8, p = 0.01) compared to the men with undetectable PSA. The same significance of PSA persistence on each study endpoint was found in the high-risk group (HR: 2.5 to 6.2, p = 0.02 to p < 0.0001). In the intermediate-risk group, PSA persistence was found as a predictor of BCR (HR: 3.9, p < 0.0001), while, in the low-risk group, PSA persistence was not detected as a significant predictor of outcomes after RP. Conclusions: Persistent PSA could be used as an independent predictor of worse long-term outcomes in high-risk PCa patients, while, in intermediate-risk patients, this parameter significantly predicts only biochemical recurrence and has no impact on the outcomes in low-risk PCa patients.
Highlights
Radical prostatectomy (RP) with or without lymph node dissection is an accepted treatment modality in patients with localized and locally advanced prostate cancer (PCa) [1,2,3].a non-negligible number of patients may experience disease recurrence following RP
The 10-year cumulative incidence of biochemical recurrence (BCR), MTS, cancer-specific mortality (CSM) and overall mortality (OM) were 39.61%, 9.70%, 4.81% and 18.15%, respectively, with a significantly higher incidence in men with prostate-specific antigen (PSA) persistence
In the multivariate regression analysis, PSA persistence was detected as an independent predictor for each study endpoint (HR: 1.8 to 5.5, p < 0.01 to p < 0.0001, see Table 2)
Summary
Radical prostatectomy (RP) with or without lymph node dissection is an accepted treatment modality in patients with localized and locally advanced prostate cancer (PCa) [1,2,3].a non-negligible number of patients may experience disease recurrence following RP. Recent reports have demonstrated an increasing interest in PSA persistence as a possible additional predictor of disease progression and cancer-specific survival [5,6,7,8,9,10,11,12,13]. The authors demonstrated the association between PSA persistence and biochemical recurrence (BCR), disease progression and cancer-specific mortality (CSM) and suggested a benefit from immediate radiotherapy [15]. In several reports, a strong association between PSA persistence and unfavorable cancer characteristics [5,7,11], there are no analyses on the importance of PSA persistence in different PCa-risk groups
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