Genomic Correlates to the Newly Proposed Grading Prognostic Groups for Prostate Cancer

被引:62
作者
Rubin, Mark A. [1 ,2 ,3 ]
Girelli, Gabriele [4 ]
Demichelis, Francesca [1 ,4 ,5 ]
机构
[1] New York Presbyterian Hosp, Weill Cornell Med Coll, Englander Inst Precis Med, New York, NY USA
[2] Weill Cornell Med Coll, Sandra & Edward Meyer Canc Ctr, New York, NY 10021 USA
[3] Weill Cornell Med Coll, Dept Pathol & Lab Med, New York, NY 10021 USA
[4] Univ Trento, Ctr Integrat Biol, Via Sommar 9, Povo, Trento, Italy
[5] Weill Cornell Med Coll, Inst Computat Biomed, New York, NY 10021 USA
关键词
Gleason grading; Prostate cancer; Genomics; Precision medicine; Active surveillance; Risk;
D O I
10.1016/j.eururo.2015.10.040
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Recommendations by the International Society of Urologic Pathology and 2016 World Health Organization blue book propose the use of a five-tiered prostate cancer (PCa) grading system. The five prognostic grade groupings (PGGs) ranging from 1 to 5 are defined as Gleason grades <= 6, 3 + 4, 4 + 3, 8, and > 8, respectively. Recent work suggests that each group is associated with a distinct risk of biochemical PCa recurrence. In this study, we sought genomic support for PGGs using whole-exome and whole-genome sequencing data for 426 clinically localized PCas treated by radical prostatectomy. After adjustment for tumor purity for the sequencing data, we observed a significant frequency increase in genomic amplifications and deletions (p = 0.013) and in nonsynonymous point mutations (p = 0.008) with increasing risk group. Interestingly, PGG1 (low risk) was entirely haploid, whereas PGG2-5 exhibited increasing polyploidy frequency. Principal component analysis of genomic profiles revealed that PGG1, PGG2, and PGG3 represent distinct classes, but PGG4 and PGG5 exhibit genomic similarity. Together, these observations for the largest PCa genomic data set to date provide support for increasing genomic alterations with increasing PGG. This is the first genomic correlation of the PGG system. Future work will need to explore the clinical utility of PGGs in prospective studies with long-term follow-up. (C) 2015 European Association of Urology.
引用
收藏
页码:557 / 560
页数:4
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