Prevalence of TMPRSS2-ERG fusion prostate cancer among men undergoing prostate biopsy in the United States.

TitlePrevalence of TMPRSS2-ERG fusion prostate cancer among men undergoing prostate biopsy in the United States.
Publication TypeJournal Article
Year of Publication2009
AuthorsMosquera J-M, Mehra R, Regan MM, Perner S, Genega EM, Bueti G, Shah RB, Gaston S, Tomlins SA, Wei JT, Kearney MC, Johnson LA, Tang JM, Chinnaiyan AM, Rubin MA, Sanda MG
JournalClin Cancer Res
Date Published2009 Jul 15
KeywordsAged, Biopsy, Gene Frequency, Humans, In Situ Hybridization, Fluorescence, Logistic Models, Male, Middle Aged, Multivariate Analysis, Oncogene Proteins, Fusion, Prospective Studies, Prostate, Prostate-Specific Antigen, Prostatic Neoplasms, Serine Endopeptidases, Trans-Activators, United States

PURPOSE: Fusion of the TMPRSS2 prostate-specific gene with the ERG transcription factor is a putatively oncogenic gene rearrangement that is commonly found in prostate cancer tissue from men undergoing prostatectomy. However, the prevalence of the fusion was less common in samples of transurethral resection of the prostate from a Swedish cohort of patients with incidental prostate cancer followed by watchful waiting, raising the question as to whether the high prevalence in prostatectomy specimens reflects selection bias. We sought to determine the prevalence of TMPRSS2-ERG gene fusion among prostate-specific antigen-screened men undergoing prostate biopsy in the United States.

EXPERIMENTAL DESIGN: We studied 140 prostate biopsies from the same number of patients for TMPRSS2-ERG fusion status with a fluorescent in situ hybridization assay. One hundred and thirty-four samples (100 cancer and 34 benign) were assessable.

RESULTS: ERG gene rearrangement was detected in 46% of prostate biopsies that were found to have prostate cancer and in 0% of benign prostate biopsies (P < 0.0001). Evaluation of morphologic features showed that cribriform growth, blue-tinged mucin, macronucleoli, and collagenous micronodules were significantly more frequent in TMPRSS2-ERG fusion-positive prostate cancer biopsies than gene fusion-negative prostate cancer biopsies (P < or = 0.04). No significant association with Gleason score was detected. In addition, non-Caucasian patients were less likely to have positive fusion status (P = 0.02).

CONCLUSIONS: This is the first prospective North American multicenter study to characterize TMPRSS2-ERG prostate cancer prevalence in a cohort of patients undergoing needle biopsy irrespective of whether or not they subsequently undergo prostatectomy. Our results show that this gene rearrangement is common among North American men who have prostate cancer on biopsy, is absent in benign prostate biopsy, and is associated with specific morphologic features. These findings indicate a need for prospective studies to evaluate the relationship of TMPRSS2-ERG rearrangement with clinical course of screening-detected prostate cancer in North American men, and a need for the development of noninvasive screening tests to detect TMPRSS2-ERG rearrangement.

Alternate JournalClin. Cancer Res.
PubMed ID19584163
PubMed Central IDPMC3717524
Grant ListP50 CA090381 / CA / NCI NIH HHS / United States
P50 CA69568 / CA / NCI NIH HHS / United States
R01AG21404 / AG / NIA NIH HHS / United States
U01 CA113913 / CA / NCI NIH HHS / United States
U01 CA113913 / CA / NCI NIH HHS / United States