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高危人群前列腺癌预防试验风险计算器的评估。

Evaluation of the Prostate Cancer Prevention Trial Risk calculator in a high-risk screening population.

机构信息

Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, USA.

出版信息

BJU Int. 2010 Feb;105(3):334-7. doi: 10.1111/j.1464-410X.2009.08793.x. Epub 2009 Aug 25.

Abstract

STUDY TYPE

Diagnostic (exploratory cohort).

LEVEL OF EVIDENCE

2b.

OBJECTIVE

To evaluate the Prostate Cancer Prevention Trial (PCPT) risk calculator in a screening cohort of young, racially diverse, high-risk men with a low baseline prostate-specific antigen (PSA) level and enrolled in the Prostate Cancer Risk Assessment Program (PRAP). The PCPT calculator provides an assessment of prostate cancer risk based on age, PSA level, race, previous biopsy, and family history.

PATIENTS AND METHODS

Eligibility for PRAP includes men aged 35-69 years who are African-American, have a family history of prostate cancer, or have a known BRCA1/2 mutation. PCPT risk scores were determined for PRAP participants, and were compared to observed prostate cancer rates.

RESULTS

In all, 624 participants were evaluated, including 382 (61.2%) African-American men and 242 (38.7%) men with a family history of prostate cancer; the median (range) age was 49.0 (34.0-69.0) years and the median PSA level 0.9 (0.1-27.2) ng/mL. The PCPT risk score correlated with prostate cancer diagnosis, as the median baseline risk score in patients diagnosed with prostate cancer was 31.3%, vs 14.2% in patients not diagnosed with prostate cancer (P < 0.001). The PCPT calculator similarly stratified the risk of diagnosis of Gleason score > or =7 disease, as the median risk score was 36.2% in patients diagnosed with Gleason > or =7 prostate cancer vs 15.2% in all other participants (P < 0.001).

CONCLUSION

The PCPT risk calculator score was found to stratify prostate cancer risk in a cohort of young, primarily African-American men with a low baseline PSA level. These results support further evaluation of this predictive tool for assessing the risk of prostate cancer in high-risk men.

摘要

研究类型

诊断(探索性队列)。

证据水平

2b。

目的

评估前列腺癌预防试验(PCPT)风险计算器在一个筛查队列中的表现,该队列包括年轻、种族多样化、高风险、基线前列腺特异性抗原(PSA)水平较低且参加前列腺癌风险评估计划(PRAP)的男性。PCPT 计算器根据年龄、PSA 水平、种族、既往活检和家族史评估前列腺癌风险。

患者和方法

PRAP 的入选标准包括年龄 35-69 岁的非裔美国男性、有前列腺癌家族史或已知 BRCA1/2 突变的男性。为 PRAP 参与者确定了 PCPT 风险评分,并与观察到的前列腺癌发生率进行了比较。

结果

共评估了 624 名参与者,其中 382 名(61.2%)为非裔美国男性,242 名(38.7%)有前列腺癌家族史;中位(范围)年龄为 49.0(34.0-69.0)岁,中位 PSA 水平为 0.9(0.1-27.2)ng/mL。PCPT 风险评分与前列腺癌诊断相关,因为诊断为前列腺癌的患者的基线风险评分中位数为 31.3%,而未诊断为前列腺癌的患者为 14.2%(P<0.001)。PCPT 计算器同样对 Gleason 评分>或=7 疾病的诊断风险进行了分层,因为诊断为 Gleason>或=7 前列腺癌的患者的中位风险评分为 36.2%,而所有其他患者的风险评分为 15.2%(P<0.001)。

结论

在一个基线 PSA 水平较低的年轻、主要为非裔美国男性队列中,PCPT 风险计算器评分被发现能够对前列腺癌风险进行分层。这些结果支持进一步评估该预测工具在评估高危男性前列腺癌风险中的作用。

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