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Volume 96, Issue 1, Pages 34-37 (July 2010)


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Outcomes from Gleason 7, intermediate risk, localized prostate cancer treated with Iodine-125 monotherapy over 10years

Nicholas P. MunrodCorresponding Author Informationemail address, Bashar Al-Qaisiehb, Peter Bownesb, Jonathan Smithc, Brendan Careyc, David Bottomleya, Dan Asha, Ann M. Henrya

Received 6 February 2009; received in revised form 27 February 2010; accepted 7 March 2010. published online 02 April 2010.

Abstract 

Background and purpose

The effect of predominating Gleason grade (3+4 versus 4+3) in Gleason sum score (GS) 7 prostate cancer (PCa) on brachytherapy outcomes is unclear. The 10year experience of permanent brachytherapy monotherapy at a single UK centre for GS 7, intermediate risk (Memorial Sloan-Kettering model), PSA10ng/ml, localised PCa is reported.

Materials and methods

Between 1995 and 2004, the outcomes of 187 patients with GS 7 PCa (PSA10ng/ml) were analysed from a cohort of 1298 men treated with permanent Iodine-125 prostate brachytherapy, including PSA relapse-free survival (PSA-RFS).

Results

Median follow-up was 5.0years (range 2.0–10.1years). One patient has died of PCa. At 10years, PSA-RFS was 82.4%/78% (ASTRO consensus and nadir +2 definitions). For GS 3+4, 5year PSA-RFS was 86.7%/87.9% and for GS 4+3: 85.2%/96.6% respectively, with no significant difference between groups. Five year PSA-RFS (ASTRO) of 92.6% was seen for D90140Gy (50% total), compared with 77.0% below 140Gy (p=0.08).

Conclusions

Iodine-125 brachytherapy monotherapy achieved good rates of medium term biochemical control in GS 7, intermediate risk localised PCa patients. There was a trend to improved outcomes in men with a D90 in excess of 140Gy.

a Department of Clinical Oncology, St James’s Institute of Oncology, St James’s University Hospital, Leeds, UK

b Department of Medical Physics, St James’s Institute of Oncology, St James’s University Hospital, Leeds, UK

c Department of Clinical Radiology, St James’s Institute of Oncology, St James’s University Hospital, Leeds, UK

d Department of Urology, St James’s Institute of Oncology, St James’s University Hospital, Leeds, UK

Corresponding Author InformationCorresponding author. Address: 48 Franklin road, Harrogate, North Yorkshire, HG1 5EE, UK.

PII: S0167-8140(10)00155-6

doi:10.1016/j.radonc.2010.03.004


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