Volume 18, Issue 4 (July 2016) 18, 575–579; DOI: 10.4103/1008-682X.175096
Clinically available RNA profiling tests of prostate tumors: utility and comparison
Rong Na1,2, Yishuo Wu1,2, Qiang Ding1,2, Jianfeng Xu1,2,3
1 Fudan Institute of Urology, Huashan Hospital, Fudan University, Shanghai; Department of Urology, Huashan Hospital, Fudan University, Shanghai, PR China 2 Fudan Institute of Urology, Huashan Hospital, Fudan University, Shanghai, PR China; Department of Urology, Huashan Hospital, Fudan University, Shanghai, PR China; Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, IL, USA,
Correspondence: R Na (narong.hs@gmail.com)
1-3-2016
Abstract |
In the postscreening era, physicians are in need of methods to discriminate aggressive from nonaggressive prostate cancer (PCa) to reduce overdiagnosis and overtreatment. However, studies have shown that prognoses (e.g., progression and mortality) differ even among individuals with similar clinical and pathological characteristics. Existing risk classifiers (TMN grading system, Gleason score, etc.) are not accurately enough to represent the biological features of PCa. Using new genomic technologies, novel biomarkers and classifiers have been developed and shown to add value to clinical or pathological risk factors for predicting aggressive disease. Among them, RNA testing (gene expression analysis) is useful because it can not only reflect genetic variations but also reflect epigenetic regulations. Commercially available RNA profiling tests (Oncotype Dx, Prolaris, and Decipher) have demonstrated strong abilities to discriminate PCa with poor prognosis from less aggressive diseases. For instance, these RNA profiling tests can predict disease progression in active surveillance patients or early recurrence after radical treatments. These tests may offer more dependable methods for PCa prognosis prediction to make more accurate and personal medical decisions.
Keywords: precision medicine; prostate cancer; RNA profiling
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