Center for Genetic Epidemiology, Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California.
Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Cancer Epidemiol Biomarkers Prev. 2020 Jul;29(7):1381-1388. doi: 10.1158/1055-9965.EPI-19-1560. Epub 2020 May 8.
BACKGROUND: The four-kallikrein (4K) panel has been demonstrated to improve prediction of aggressive prostate cancer compared with prostate-specific antigen (PSA) among men with moderately elevated PSA levels. However, the development and testing of the 4K panel has been conducted primarily in White men, with limited data in African Americans and no studies in other racial and ethnic groups. METHODS: We evaluated the 4K panel in a nested case-control study among African American, Latino, Japanese, Native Hawaiian, and White men in the Multiethnic Cohort. Prediagnostic blood levels of free, intact, and total PSA and human kallikrein-related peptidase 2 were measured among 1,667 incident prostate cancer cases and 691 controls with PSA ≥2 ng/mL. We evaluated the discriminative ability of the 4K panel within and across all racial/ethnic groups. RESULTS: The 4K panel enhanced discrimination of overall prostate cancer compared with free plus total PSA and total PSA alone (AUC 0.748 vs. 0.711 and 0.669, respectively). Discrimination was further enhanced for Gleason 8+ prostate cancer, aggressive prostate cancer, and death due to prostate cancer, and to a lesser degree for nonaggressive prostate cancer. Improvement of the 4K panel over PSA was observed in each population. Adding a prostate cancer polygenic risk score slightly improved upon the discriminative ability of the 4K panel. CONCLUSIONS: The superior discriminative ability of the 4K panel over PSA for overall and aggressive prostate cancer across multiethnic populations indicates the broad clinical applicability of the 4K panel. IMPACT: Our multiethnic investigation suggests potential for the 4K panel to improve current prostate cancer screening practices.
背景:与前列腺特异性抗原(PSA)相比,四激肽(4K)panel 已被证明可提高中度 PSA 升高男性中侵袭性前列腺癌的预测能力。然而,4K panel 的开发和测试主要是在白人男性中进行的,在非裔美国人和其他种族和民族群体中数据有限,没有研究。 方法:我们在多民族队列中进行了一项嵌套病例对照研究,评估了非洲裔美国人、拉丁裔、日本裔、夏威夷原住民和白种人男性中的 4K panel。在 1667 例前列腺癌病例和 691 例 PSA≥2ng/ml 的对照中,测量了游离、完整和总 PSA 以及人激肽释放酶相关肽 2 的预测性血液水平。我们评估了 4K panel 在所有种族/民族群体中的区分能力。 结果:与游离加总 PSA 和总 PSA 相比,4K panel 增强了对总体前列腺癌的区分能力(AUC 分别为 0.748、0.711 和 0.669)。对 Gleason 8+前列腺癌、侵袭性前列腺癌和前列腺癌死亡的区分能力进一步增强,对非侵袭性前列腺癌的区分能力略有增强。在每个群体中,4K panel 对 PSA 的改善都有所提高。添加前列腺癌多基因风险评分略微提高了 4K panel 的区分能力。 结论:4K panel 在多民族人群中对总体和侵袭性前列腺癌的 PSA 具有优越的区分能力,表明 4K panel 具有广泛的临床应用潜力。 影响:我们的多民族研究表明,4K panel 有可能改善当前的前列腺癌筛查实践。
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