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Circulating estradiol, but not testosterone, is a significant predictor of high‐grade prostate cancer in patients undergoing radical prostatectomy
Author(s) -
Salonia Andrea,
Gallina Andrea,
Briganti Alberto,
Suardi Nazareno,
Capitanio Umberto,
Abdollah Firas,
Bertini Roberto,
Freschi Massimo,
Rigatti Patrizio,
Montorsi Francesco
Publication year - 2011
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.26136
Subject(s) - medicine , prostate cancer , prostatectomy , urology , sex hormone binding globulin , prostate specific antigen , radical retropubic prostatectomy , univariate analysis , prostate biopsy , testosterone (patch) , body mass index , logistic regression , prostate , odds ratio , cancer , gynecology , hormone , multivariate analysis , androgen
BACKGROUND: The objective of this study was to assess the association between preoperative circulating levels of 17β‐estradiol (E 2 ) and high‐grade prostate cancer (HGPCa) (Gleason grade ≥4 + 3) at the time patients underwent radical retropubic prostatectomy (RRP). METHODS: Serum total testosterone (tT), sex hormone‐binding globulin (SHBG), and E 2 levels were measured the day before surgery (8‐10 AM ) in a cohort of 655 consecutive Caucasian‐ European patients who underwent RRP at a single institution. Logistic regression models were used to test the association between predictors (including age, body mass index, prostate‐specific antigen [PSA], clinical tumor classification, biopsy Gleason sum, tT, SHBG, and E 2 ) and HGPCa. Serum E 2 was included in the model as both a continuous variable and a categorized variable (according to the most informative cutoff: 50 pg/mL). RESULTS: Pathologic HGPCa was identified in 156 patients (23.8%). Patients with HGPCa had significantly higher PSA, clinical tumor classification, and biopsy Gleason sum than those without HGPCa (all P < .001). No other significant differences were observed between groups. At univariate analysis, continuously coded E 2 was not associated significantly with HGPCa (odds ratio [OR], 1.009; P = .25), whereas patients with E 2 levels ≥50 pg/mL had a 3.24‐fold increased risk of HGPCa ( P < .001). At multivariate analysis, E 2 was associated significantly with HGPCa both as a continuous predictor (OR, 1.02; P = .04) and as a categorical predictor (OR, 3.94; P < .001) after accounting for other variables. Conversely, tT and SHBG levels were not associated significantly with HGPCa. CONCLUSIONS: E 2 was associated significantly with pathologic HGPCa, whereas SHBG and tT failed to demonstrate any association with HGPCa in patients who underwent RRP. Cancer 2011;. © 2011 American Cancer Society.