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Oncotype DX前列腺癌检测在新诊断前列腺癌男性患者临床治疗选择中的应用:一项回顾性图表审查分析

Utility of the Oncotype DX Prostate Cancer Assay in Clinical Practice for Treatment Selection in Men Newly Diagnosed with Prostate Cancer: A Retrospective Chart Review Analysis.

作者信息

Dall'Era Marc A, Maddala Tara, Polychronopoulos Louise, Gallagher Jack R, Febbo Phillip G, Denes Béla S

机构信息

Department of Urology, University of California Davis School of Medicine, Sacramento, California.

Genomic Health, Inc., Redwood City, California.

出版信息

Urol Pract. 2015 Nov;2(6):343-348. doi: 10.1016/j.urpr.2015.02.007. Epub 2015 Jul 8.

Abstract

INTRODUCTION

The 17-gene Oncotype DX® prostate cancer assay (Genomic Health Inc., Redwood City, California) is a validated, biopsy based gene expression assay that reports the Genomic Prostate Score. Combined with clinical risk features, Genomic Prostate Score provides an individualized estimation of disease aggressiveness at diagnosis. With this retrospective chart review we assessed the impact of incorporating the Oncotype DX Genomic Prostate Score on treatment recommendations and decisions for men with newly diagnosed low risk prostate cancer in community urology practices.

METHODS

A total of 24 urologists who ordered the Oncotype DX prostate cancer assay soon after launch (May 2013) were invited to participate in the study. Clinicopathological data, Genomic Prostate Score results and treatment related information were retrieved from medical records. Data also were collected for a pre-Genomic Prostate Score baseline group diagnosed from May 2012 to April 2013. Descriptive analyses were performed to evaluate the proportion of men for whom active surveillance was recommended and used before and after the availability of Genomic Prostate Score.

RESULTS

Overall 15 physicians contributing 211 patients (Genomic Prostate Score group 124, baseline group 87) participated in the chart review. Patients in the Genomic Prostate Score and baseline groups had comparable risk based on traditional clinical pathological features, with 82% with NCCN® very low or low risk disease. With Genomic Prostate Score the relative increase in active surveillance recommended was 22% (baseline 50% and Genomic Prostate Score 61%, absolute increase of 11%) and the relative increase in use of active surveillance was 56% (baseline 43% and Genomic Prostate Score 67%, absolute increase of 24%). Treatment recommendations for active surveillance were directionally consistent with assay reported risk.

CONCLUSIONS

Genomic Prostate Score testing was associated with greater physician recommendation of and use of active surveillance in community clinical practices.

摘要

引言

17基因Oncotype DX®前列腺癌检测(加利福尼亚州红木城的基因组健康公司)是一种经过验证的、基于活检的基因表达检测,可报告基因组前列腺评分。结合临床风险特征,基因组前列腺评分可在诊断时对疾病侵袭性进行个体化评估。通过这项回顾性图表审查,我们评估了纳入Oncotype DX基因组前列腺评分对社区泌尿外科实践中初诊低风险前列腺癌男性患者治疗建议和决策的影响。

方法

共有24位在该检测推出后不久(2013年5月)就订购了Oncotype DX前列腺癌检测的泌尿科医生受邀参与该研究。从病历中检索临床病理数据、基因组前列腺评分结果和治疗相关信息。还收集了2012年5月至2013年4月诊断的基因组前列腺评分前基线组的数据。进行描述性分析以评估在基因组前列腺评分可用前后建议并采用主动监测的男性比例。

结果

总体上,15位医生贡献了211例患者(基因组前列腺评分组124例,基线组87例)参与了图表审查。基于传统临床病理特征,基因组前列腺评分组和基线组患者的风险相当,82%患有NCCN®极低或低风险疾病。有了基因组前列腺评分后,建议进行主动监测的相对增加率为22%(基线为50%,基因组前列腺评分为61%,绝对增加11%),主动监测的使用相对增加率为56%(基线为43%,基因组前列腺评分为67%,绝对增加24%)。主动监测的治疗建议与检测报告的风险在方向上一致。

结论

在社区临床实践中,基因组前列腺评分检测与医生更多地建议和采用主动监测相关。

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