PT  - JOURNAL ARTICLE
AU  - Gurel, Bora
AU  - Lucia, M. Scott
AU  - Thompson, Ian M.
AU  - Goodman, Phyllis J.
AU  - Tangen, Catherine M.
AU  - Kristal, Alan R.
AU  - Parnes, Howard L.
AU  - Hoque, Ashraful
AU  - Lippman, Scott M.
AU  - Sutcliffe, Siobhan
AU  - Peskoe, Sarah B.
AU  - Drake, Charles G.
AU  - Nelson, William G.
AU  - De Marzo, Angelo M.
AU  - Platz, Elizabeth A.
TI  - Chronic Inflammation in Benign Prostate Tissue Is Associated with High-Grade Prostate Cancer in the Placebo Arm of the Prostate Cancer Prevention Trial
AID  - 10.1158/1055-9965.EPI-13-1126
DP  - 2014 May 01
TA  - Cancer Epidemiology Biomarkers & Prevention
PG  - 847--856
VI  - 23
IP  - 5
4099  - http://cebp.aacrjournals.org/content/23/5/847.short
4100  - http://cebp.aacrjournals.org/content/23/5/847.full
SO  - Cancer Epidemiol Biomarkers Prev2014 May 01; 23
AB  - Background: Chronic inflammation is hypothesized to influence prostate cancer development, although a definitive link has not been established. Methods: Prostate cancer cases (N = 191) detected on a for-cause (clinically indicated) or end-of-study (protocol directed) biopsy, and frequency-matched controls (N = 209), defined as negative for cancer on an end-of-study biopsy, were sampled from the placebo arm of the Prostate Cancer Prevention Trial. Inflammation prevalence and extent in benign areas of biopsy cores were visually assessed using digital images of hematoxylin and eosin–stained sections. Logistic regression was used to estimate associations. Results: Of note, 86.2% of cases and 78.2% of controls had at least one biopsy core (of three assessed) with inflammation in benign areas, most of which was chronic. Men who had at least one biopsy core with inflammation had 1.78 [95% confidence interval (CI), 1.04–3.06] times the odds of prostate cancer compared with men who had zero cores with inflammation. The association was stronger for high-grade disease (Gleason sum 7–10, N = 94; OR, 2.24; 95% CI, 1.06–4.71). These patterns were present when restricting to cases and controls in whom intraprostatic inflammation was the least likely to have influenced biopsy recommendation because their prostate-specific antigen (PSA) was low (<2 ng/mL at biopsy). Conclusion: Inflammation, most of which was chronic, was common in benign prostate tissue, and was positively associated with prostate cancer, especially high grade. The association did not seem to be due to detection bias. Impact: This study supports an etiologic link between inflammation and prostate carcinogenesis, and suggests an avenue for prevention by mitigating intraprostatic inflammation. Cancer Epidemiol Biomarkers Prev; 23(5); 847–56. ©2014 AACR.