TY - JOUR
T1 - Effect of dutasteride on prostate biopsy rates and the diagnosis of prostate cancer in men with lower urinary tract symptoms and enlarged prostates in the combination of avodart and Tamsulosin trial
AU - Roehrborn, Claus G.
AU - Andriole, Gerald L.
AU - Wilson, Timothy H.
AU - Castro, Ramiro
AU - Rittmaster, Roger S.
N1 - Funding Information:
Acknowledgments: Editorial support in the form of writing the first draft, collating author comments, and assembling figures and tables was provided by Helen Farrington and Meredith Kalish of Choice Pharma and funded by GlaxoSmithKline.
Funding Information:
Funding/Support and role of the sponsor: This study was supported by GlaxoSmithKline (GSK). GSK was involved in the design and conduct of the study; in collection, management, analysis, and interpretation of the data; and in preparation, review, and approval of the manuscript.
PY - 2011/2
Y1 - 2011/2
N2 - Background: A 23% relative risk reduction (RRR) in prostate cancer (PCa) was shown in men receiving dutasteride in the 4-yr Reduction by Dutasteride of Prostate Cancer Events study, in whom biopsies were protocol dependent. Objective: Our aim was to explore PCa risk reduction in men with benign prostatic hyperplasia (BPH) from the Combination of Avodart and Tamsulosin (CombAT) study, in which biopsies were undertaken for cause. Design, setting, and participants: CombAT was a 4-yr randomized double-blind parallel group study in 4844 men ≥50 yr of age with clinically diagnosed moderate to severe BPH, International Prostate Symptom Score ≥12, prostate volume ≥30 ml, and serum prostate-specific antigen (PSA) 1.5-10 ng/ml. Men underwent annual PSA measurement and digital rectal examination (DRE), and prostate biopsies were performed for cause. Intervention: All patients took tamsulosin 0.4 mg/d, dutasteride 0.5 mg/d, or a combination of both. Measurements: The primary end point was incidence of PCa. Secondary end points included postbaseline prostate biopsy rates and Gleason score of cancers. Results and limitations: Dutasteride (alone or in combination with tamsulosin) was associated with a 40% RRR of PCa diagnosis compared with tamsulosin monotherapy (95% confidence interval, 16-57%; p = 0.002) and a 40% reduction in the likelihood of biopsy. There were similar reductions in low- and high-grade Gleason score cancers. The biopsy rate in the groups receiving dutasteride trended toward a higher diagnostic yield (combination: 29%, dutasteride: 28%, tamsulosin: 24%). One limitation was the lack of a standardized approach to PCa diagnosis and grading. Conclusions: Dutasteride, alone or in combination with tamsulosin, significantly reduced the relative risk of PCa diagnosis in men with BPH undergoing annual DRE and PSA screening. Consistent with the increased usefulness of PSA for PCa detection, men receiving dutasteride had a numerically lower biopsy rate and higher yield of PCa on biopsy.
AB - Background: A 23% relative risk reduction (RRR) in prostate cancer (PCa) was shown in men receiving dutasteride in the 4-yr Reduction by Dutasteride of Prostate Cancer Events study, in whom biopsies were protocol dependent. Objective: Our aim was to explore PCa risk reduction in men with benign prostatic hyperplasia (BPH) from the Combination of Avodart and Tamsulosin (CombAT) study, in which biopsies were undertaken for cause. Design, setting, and participants: CombAT was a 4-yr randomized double-blind parallel group study in 4844 men ≥50 yr of age with clinically diagnosed moderate to severe BPH, International Prostate Symptom Score ≥12, prostate volume ≥30 ml, and serum prostate-specific antigen (PSA) 1.5-10 ng/ml. Men underwent annual PSA measurement and digital rectal examination (DRE), and prostate biopsies were performed for cause. Intervention: All patients took tamsulosin 0.4 mg/d, dutasteride 0.5 mg/d, or a combination of both. Measurements: The primary end point was incidence of PCa. Secondary end points included postbaseline prostate biopsy rates and Gleason score of cancers. Results and limitations: Dutasteride (alone or in combination with tamsulosin) was associated with a 40% RRR of PCa diagnosis compared with tamsulosin monotherapy (95% confidence interval, 16-57%; p = 0.002) and a 40% reduction in the likelihood of biopsy. There were similar reductions in low- and high-grade Gleason score cancers. The biopsy rate in the groups receiving dutasteride trended toward a higher diagnostic yield (combination: 29%, dutasteride: 28%, tamsulosin: 24%). One limitation was the lack of a standardized approach to PCa diagnosis and grading. Conclusions: Dutasteride, alone or in combination with tamsulosin, significantly reduced the relative risk of PCa diagnosis in men with BPH undergoing annual DRE and PSA screening. Consistent with the increased usefulness of PSA for PCa detection, men receiving dutasteride had a numerically lower biopsy rate and higher yield of PCa on biopsy.
KW - Benign prostatic hyperplasia
KW - Biopsy
KW - Dutasteride
KW - Prevention and control
KW - Prostate cancer
KW - Risk reduction
KW - Tamsulosin
UR - http://www.scopus.com/inward/record.url?scp=78650684271&partnerID=8YFLogxK
U2 - 10.1016/j.eururo.2010.10.040
DO - 10.1016/j.eururo.2010.10.040
M3 - Article
C2 - 21093145
AN - SCOPUS:78650684271
SN - 0302-2838
VL - 59
SP - 244
EP - 249
JO - European Urology
JF - European Urology
IS - 2
ER -