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Volume 93, Issue 2, Pages 185-191 (November 2009)


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Radical prostatectomy vs. intensity-modulated radiation therapy in the management of localized prostate adenocarcinoma

Ayal A. AizeraCorresponding Author Informationemail address, James B. Yua, John W. Colbergb, Anne M. McKeona, Roy H. Deckera, Richard E. Peschela

Received 15 May 2009; received in revised form 25 August 2009; accepted 1 September 2009. published online 05 October 2009.

Abstract 

Background and purpose

To determine whether radical prostatectomy (RP) or intensity-modulated radiation therapy (IMRT) to ⩾72Gy, plus hormonal therapy if indicated, results in improved biochemical disease-free survival (BDFS) in localized prostate adenocarcinoma.

Materials and methods

Between 1997 and 2005, a consecutive sample of 556 patients who underwent RP (n=204) or IMRT (n=352) at two referral centers was analyzed. The patients were stratified into prognostic groups based on clinical stage, Gleason score, and pretreatment prostate-specific antigen (PSA). The outcome measure was BDFS.

Results

IMRT patients had more advanced disease at baseline (p<.001). There was no difference in five-year BDFS rates between RP and IMRT in the favorable (92.8% vs. 85.3%, p=.20) or intermediate prognosis (86.7% vs. 82.2%, p=.46) subsets. A difference favoring IMRT plus hormonal therapy was seen in the poor prognosis (38.4% vs. 62.2%, p<.001) subset. Within the entire cohort, after adjustment for confounding variables, Gleason score (p<.001) and clinical stage (p<.001) predicted BDFS, but treatment modality (p=.06) did not. Within the poor prognosis subset, treatment modality (p=.006) predicted BDFS.

Conclusions

BDFS is similar between RP and IMRT for patients with a favorable or intermediate prognosis. Patients with a poor prognosis display higher BDFS when treated with IMRT to ⩾72Gy plus hormonal therapy.

a Department of Therapeutic Radiology, Yale School of Medicine, New Haven, CT, USA

b Section of Urology, Department of Surgery, Yale School of Medicine, New Haven, CT, USA

Corresponding Author InformationCorresponding author. Address: Department of Therapeutic Radiology, Yale School of Medicine, PO Box 208040, New Haven, CT 06510, USA.

PII: S0167-8140(09)00498-8

doi:10.1016/j.radonc.2009.09.001


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