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对接受5-α还原酶抑制剂治疗的良性前列腺增生男性患者的前列腺特异性抗原监测:西班牙和巴西泌尿外科医生真实临床实践的非干预性横断面研究

Monitoring of prostate-specific antigen in men with benign prostate enlargement receiving 5-alpha reductase inhibitors: a non-interventional, cross-sectional study of real-world practice of urologists in Spain and Brazil.

作者信息

Palacios Juan Manuel, Kapse Pratiksha, Cortes Vanessa, Averbeck Marcio Augusto, Alba Alberto Budia, Somvanshi Suryakant, da Costa Cruz Danilo Souza Lima, Pereira Fiona

机构信息

Global Medical Urology, GSK, Madrid, Spain.

Global Medical Urology, GSK, Mumbai, India.

出版信息

BMC Urol. 2025 Jan 31;25(1):22. doi: 10.1186/s12894-025-01701-1.

Abstract

BACKGROUND

Inconsistent monitoring of prostate-specific antigen in patients receiving 5-alpha reductase inhibitors for lower urinary tract symptoms/benign prostate enlargement may affect prostate cancer outcomes. This study evaluated real-world practice among urologists treating patients receiving 5-alpha reductase inhibitors.

METHODS

This non-interventional, cross-sectional study collected data from urologists in Spain (N = 100) and Brazil (N = 100) via a self-reporting questionnaire and patient record forms. Endpoints included: frequency/methodology of prostate-specific antigen monitoring, concerns about the effect of 5-alpha reductase inhibitors on prostate-specific antigen monitoring, triggers of prostate biopsy, and concerns when switching 5-alpha reductase inhibitor formulation.

RESULTS

Over half of urologists monitored prostate-specific antigen every 6 months (Spain 59%, Brazil 58%). Preferred methods were the "doubling rule" (Spain 66%, Brazil 41%) and "increase from nadir" (Spain 28%, Brazil 43%). A minority of urologists monitored unadjusted values (Spain 3%, Brazil 11%) or did not monitor prostate-specific antigen (Spain 1%, Brazil 3%). Most urologists ranked the potential for 5-alpha reductase inhibitors to mask prostate cancer as their top concern (Spain 65%, Brazil 56%). The most selected trigger for prostate biopsy was "if doubled (adjusted) prostate-specific antigen level after 6 months of treatment is > 4 ng/mL" (Spain 39%, Brazil 37%). Many urologists were moderately/very concerned about the effect on prostate-specific antigen when switching 5-alpha reductase inhibitor formulation.

CONCLUSIONS

An unmet need exists for standard guidance and continuous education to support optimal monitoring and interpretation of prostate-specific antigen in patients with lower urinary tract symptoms/benign prostate enlargement treated with 5-alpha reductase inhibitors.

摘要

背景

在接受5-α还原酶抑制剂治疗下尿路症状/良性前列腺增生的患者中,对前列腺特异性抗原的监测不一致可能会影响前列腺癌的治疗结果。本研究评估了治疗接受5-α还原酶抑制剂患者的泌尿外科医生的实际临床实践。

方法

这项非干预性横断面研究通过自我报告问卷和患者记录表收集了西班牙(N = 100)和巴西(N = 100)泌尿外科医生的数据。研究终点包括:前列腺特异性抗原监测的频率/方法、对5-α还原酶抑制剂对前列腺特异性抗原监测影响的担忧、前列腺活检的触发因素以及更换5-α还原酶抑制剂剂型时的担忧。

结果

超过一半的泌尿外科医生每6个月监测一次前列腺特异性抗原(西班牙为59%,巴西为58%)。首选方法是“倍增规则”(西班牙为66%,巴西为41%)和“从最低点升高”(西班牙为28%,巴西为43%)。少数泌尿外科医生监测未经调整的值(西班牙为3%,巴西为11%)或不监测前列腺特异性抗原(西班牙为1%,巴西为3%)。大多数泌尿外科医生将5-α还原酶抑制剂掩盖前列腺癌的可能性列为首要担忧(西班牙为65%,巴西为56%)。前列腺活检最常选择的触发因素是“治疗6个月后调整后的前列腺特异性抗原水平翻倍且>4 ng/mL”(西班牙为39%,巴西为37%)。许多泌尿外科医生对更换5-α还原酶抑制剂剂型时对前列腺特异性抗原的影响存在中度/非常担忧。

结论

在接受5-α还原酶抑制剂治疗下尿路症状/良性前列腺增生的患者中,对于支持前列腺特异性抗原的最佳监测和解读,标准指南和持续教育存在未满足的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51c/11786547/a2b22f6934d0/12894_2025_1701_Fig1_HTML.jpg

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