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本文引用的文献

1
Limited ability of existing nomograms to predict outcomes in men undergoing active surveillance for prostate cancer.现有列线图在预测接受前列腺癌主动监测男性患者预后方面的能力有限。
BJU Int. 2014 Dec;114(6b):E18-E24. doi: 10.1111/bju.12554. Epub 2014 Feb 20.
2
Factors influencing disease progression of prostate cancer under active surveillance: a McGill University Health Center cohort.主动监测下影响前列腺癌疾病进展的因素:麦吉尔大学健康中心队列研究
BJU Int. 2014 Dec;114(6b):E99-E104. doi: 10.1111/bju.12754. Epub 2014 Aug 11.
3
ERG protein expression in diagnostic specimens is associated with increased risk of progression during active surveillance for prostate cancer.在前列腺癌主动监测中,诊断标本中 ERG 蛋白的表达与进展风险增加相关。
Eur Urol. 2014 Nov;66(5):851-60. doi: 10.1016/j.eururo.2014.02.058. Epub 2014 Mar 7.
4
Active surveillance for clinically localized prostate cancer--a systematic review.主动监测局限性前列腺癌——系统评价。
J Surg Oncol. 2014 Jun;109(8):830-5. doi: 10.1002/jso.23584. Epub 2014 Mar 7.
5
Role of multiparametric 3.0-Tesla magnetic resonance imaging in patients with prostate cancer eligible for active surveillance.多参数 3.0T 磁共振成像在适合主动监测的前列腺癌患者中的作用。
BJU Int. 2014 Jun;113(6):864-70. doi: 10.1111/bju.12423. Epub 2013 Dec 2.
6
Predictors of pathologic progression on biopsy among men on active surveillance for localized prostate cancer: the value of the pattern of surveillance biopsies.在对局限性前列腺癌进行主动监测的男性中,活检出现病理性进展的预测因素:监测活检模式的价值。
Eur Urol. 2014 Aug;66(2):337-42. doi: 10.1016/j.eururo.2013.08.060. Epub 2013 Sep 9.
7
Accuracy of multiparametric magnetic resonance imaging in confirming eligibility for active surveillance for men with prostate cancer.多参数磁共振成像在确认前列腺癌男性进行主动监测的适宜性方面的准确性。
Cancer. 2013 Sep 15;119(18):3359-66. doi: 10.1002/cncr.28216. Epub 2013 Jul 2.
8
Urinary TMPRSS2:ERG and PCA3 in an active surveillance cohort: results from a baseline analysis in the Canary Prostate Active Surveillance Study.主动监测队列中的尿 TMPRSS2:ERG 和 PCA3:Canary 前列腺主动监测研究中的基线分析结果。
Clin Cancer Res. 2013 May 1;19(9):2442-50. doi: 10.1158/1078-0432.CCR-12-3283. Epub 2013 Mar 20.
9
Medium-term outcomes of active surveillance for localised prostate cancer.局限性前列腺癌主动监测的中期结果。
Eur Urol. 2013 Dec;64(6):981-7. doi: 10.1016/j.eururo.2013.02.020. Epub 2013 Feb 18.
10
Active surveillance can reduce overtreatment in patients with low-risk prostate cancer.主动监测可减少低风险前列腺癌患者的过度治疗。
Dan Med J. 2013 Feb;60(2):A4575.

前列腺癌的主动监测:何时建议延迟干预。

Active surveillance for prostate cancer: when to recommend delayed intervention.

作者信息

Babaian Kara N

机构信息

Department of Urology, University of California, Irvine, Orange, CA, USA.

出版信息

Asian J Androl. 2015 Nov-Dec;17(6):885-7; discussion 886-7. doi: 10.4103/1008-682X.151396.

DOI:10.4103/1008-682X.151396
PMID:26178391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4814954/
Abstract

There are no agreed upon guidelines for placing patients on active surveillance (AS). Therefore, there are no absolute criteria for taking patients off AS and when to recommend treatment. The criteria used to define progression are currently based on prostate specific antigen (PSA) kinetics, biopsy reclassification, and change in clinical stage. Multiple studies have evaluated predictors of progression such as PSA, PSA density (PSAD), prostate volume, core positivity, and visible lesion on multiparametric magnetic resonance imaging (mpMRI). Furthermore, published nomograms designed to predict indolent prostate cancer do not perform well when used to predict progression. Newer biomarkers have also not performed well to predict progression. These findings highlight that clinical and pathologic variables are not enough to identify patients that will progress while on AS. In the future, with the use of imaging, biomarkers, and gene expression assays, we should be better equipped to diagnose/stage prostate cancer and to distinguish between insignificant and significant disease.

摘要

对于将患者置于主动监测(AS)之下,目前尚无达成共识的指南。因此,对于将患者从主动监测中移除以及何时推荐治疗,不存在绝对标准。目前用于定义疾病进展的标准基于前列腺特异性抗原(PSA)动力学、活检重新分类以及临床分期的变化。多项研究评估了疾病进展的预测因素,如PSA、PSA密度(PSAD)、前列腺体积、穿刺阳性率以及多参数磁共振成像(mpMRI)上的可见病变。此外,用于预测惰性前列腺癌的已发表列线图在用于预测疾病进展时效果不佳。新型生物标志物在预测疾病进展方面也表现不佳。这些发现表明,临床和病理变量不足以识别在主动监测期间会出现疾病进展的患者。未来,通过使用影像学、生物标志物和基因表达检测,我们应该能够更好地诊断/分期前列腺癌,并区分意义不显著和意义显著的疾病。