1. The TMPRSS2:ERG Rearrangement, ERG Expression, and Prostate Cancer Outcomes: a Cohort Study and Meta-analysis
- Author
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Andreas Pettersson, Meir J. Stampfer, Michael J. Pitt, Howard D. Sesso, Edward Giovannucci, Jennifer R. Rider, Martin G. Sanda, Philip W. Kantoff, Azra H. Ligon, Rebecca E. Graff, Lorelei A. Mucci, Michelangelo Fiorentino, Catherine A. Suppan, Richard Flavin, Scott R. Bauer, Edward C. Stack, Massimo Loda, Kathryn L. Penney, Eric L. Ding, Neil E. Martin, Christopher Sweeney, Rosina T. Lis, Lauren Kunz, Pettersson A, Graff RE, Bauer SR, Pitt MJ, Lis RT, Stack EC, Martin NE, Kunz L, Penney KL, Ligon A, Suppan C, Flavin R, Sesso H, Rider JR, Sweeney CS, Stampfer MJ, Fiorentino M, Kantoff PW, Sanda MG, Giovannucci E, Ding EL, Loda M, and Mucci LA
- Subjects
Oncology ,Biochemical recurrence ,Male ,medicine.medical_specialty ,tmprss2-erg gene fusion ,Epidemiology ,medicine.medical_treatment ,united-states ,psa recurrence ,adenocarcinomas ,in-situ hybridization ,Article ,Cohort Studies ,Prostate cancer ,Transcriptional Regulator ERG ,Internal medicine ,medicine ,favorable prognosis ,Humans ,gleason score ,Prospective cohort study ,Aged ,Neoplasm Staging ,Gynecology ,Gene Rearrangement ,Prostatectomy ,business.industry ,Serine Endopeptidases ,Prostatic Neoplasms ,Gene rearrangement ,tumor-cells ,Middle Aged ,medicine.disease ,radical prostatectomy ,Treatment Outcome ,transition zone ,Trans-Activators ,Gene Fusion ,Neoplasm Recurrence, Local ,business ,Erg ,Cohort study - Abstract
Background: Whether the genomic rearrangement transmembrane protease, serine 2 (TMPRSS2):v-ets erythroblastosis virus E26 oncogene homolog (ERG) has prognostic value in prostate cancer is unclear. Methods: Among men with prostate cancer in the prospective Physicians' Health and Health Professionals Follow-Up Studies, we identified rearrangement status by immunohistochemical assessment of ERG protein expression. We used Cox models to examine associations of ERG overexpression with biochemical recurrence and lethal disease (distant metastases or cancer-specific mortality). In a meta-analysis including 47 additional studies, we used random-effects models to estimate associations between rearrangement status and outcomes. Results: The cohort consisted of 1,180 men treated with radical prostatectomy between 1983 and 2005. During a median follow-up of 12.6 years, 266 men experienced recurrence and 85 men developed lethal disease. We found no significant association between ERG overexpression and biochemical recurrence [hazard ratio (HR), 0.99; 95% confidence interval (CI), 0.78–1.26] or lethal disease (HR, 0.93; 95% CI, 0.61–1.43). The meta-analysis of prostatectomy series included 5,074 men followed for biochemical recurrence (1,623 events), and 2,049 men followed for lethal disease (131 events). TMPRSS2:ERG was associated with stage at diagnosis [risk ratio (RR)≥T3 vs. T2, 1.23; 95% CI, 1.16–1.30) but not with biochemical recurrence (RR, 1.00; 95% CI, 0.86–1.17) or lethal disease (RR, 0.99; 95% CI, 0.47–2.09). Conclusions: These results suggest that TMPRSS2:ERG, or ERG overexpression, is associated with tumor stage but does not strongly predict recurrence or mortality among men treated with radical prostatectomy. Impact: This is the largest prospective cohort study to examine associations of ERG overexpression and lethal prostate cancer among men treated with radical prostatectomy. Cancer Epidemiol Biomarkers Prev; 21(9); 1497–509. ©2012 AACR.
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- 2012