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与当前的前列腺癌检测相比,斯德哥尔摩-3(STHLM3)模型可改善 50-69 岁男性的前列腺癌诊断。

The Stockholm-3 (STHLM3) Model can Improve Prostate Cancer Diagnostics in Men Aged 50-69 yr Compared with Current Prostate Cancer Testing.

机构信息

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden; Department of Urology, Karolinska University Hospital Solna, Stockholm, Sweden.

出版信息

Eur Urol Focus. 2018 Sep;4(5):707-710. doi: 10.1016/j.euf.2016.10.009. Epub 2016 Nov 23.

Abstract

Prostate cancer screening is associated with low specificity, unnecessary biopsies, and overdiagnosis. We have previously shown that the Stockholm-3 model (S3M) can reduce biopsies compared with using prostate-specific antigen (PSA) ≥3ng/ml as an indication for biopsy. Urologists in today's current prostate cancer testing (CPT) have access to numerous variables in addition to PSA (eg, age, ethnicity, family history, free PSA, PSA velocity, digital rectal examination, and prostate volume) to support biopsy decisions. We estimated the number of prostate cancers diagnosed and prostate biopsies performed if S3M replaced CPT in Stockholm, Sweden, by comparing biopsy results in 56 282 men who underwent PSA testing according to CPT in Stockholm in 2011 with the 47 688 men enrolled in the STHLM3 validation cohort 2012-2015. With the same sensitivity as CPT to diagnose Gleason score ≥7 prostate cancer, S3M was estimated to reduce the number of men biopsied by 53% (95% confidence interval [CI]: 41-65%), avoid 76% (95% CI: 67-81%) of negative biopsies, and reduce Gleason score 6 cancers by 23% (95% CI: 6-40%). S3M has the potential to improve prostate cancer diagnostics by better selecting men with high risk of GS ≥7 prostate cancer. PATIENT SUMMARY: We modeled the effect the Stockholm-3 model would have on prostate cancer diagnostics if it replaced current clinical practice. We found that Stockholm-3 model may substantially reduce the number of biopsies, while maintaining the same sensitivity to diagnose clinically significant prostate cancer.

摘要

前列腺癌筛查的特异性低,会导致不必要的活检和过度诊断。我们之前已经证明,Stockholm-3 模型(S3M)可以减少活检数量,与使用前列腺特异性抗原(PSA)≥3ng/ml 作为活检指征相比。与 PSA(例如年龄、种族、家族史、游离 PSA、PSA 速度、直肠指检和前列腺体积)相比,泌尿科医生在当前的前列腺癌检测(CPT)中可以获得更多变量,以支持活检决策。我们通过比较 2011 年根据 CPT 在斯德哥尔摩进行 PSA 检测的 56282 名男性的活检结果与 2012-2015 年参加 STHLM3 验证队列的 47688 名男性的活检结果,估算了如果 S3M 取代瑞典斯德哥尔摩的 CPT,会诊断出多少例前列腺癌和进行多少例前列腺活检。如果 S3M 诊断 Gleason 评分≥7 前列腺癌的敏感性与 CPT 相同,那么预计将减少 53%(95%置信区间[CI]:41-65%)接受活检的男性数量,避免 76%(95%CI:67-81%)的阴性活检,并减少 Gleason 评分 6 癌症的数量 23%(95%CI:6-40%)。S3M 有可能通过更好地选择高风险 GS≥7 前列腺癌的男性来改善前列腺癌的诊断。患者总结:我们对如果 Stockholm-3 模型取代当前的临床实践,它将对前列腺癌诊断产生的影响进行建模。我们发现,Stockholm-3 模型可能会大大减少活检数量,同时保持诊断临床显著前列腺癌的相同敏感性。

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