Abstract
Objective
To retrospectively evaluate the toxicity of low-dose-rate brachytherapy and to relate it to the dose-volume to organs at risk.
Material and methods
We study 160 patients with early prostate cancer, treated with 125-I implants. Most of them were T1c (63.1%), T2a (35.6%) and Gleason ≤6 (96.2%). Median PSA was 7.2 ng/ml (2.3–13.5); 85.6% were low-risk cases and 14.4% high-risk cases. Mean follow-up was 24 months (7–48).
Results
Acute urinary toxicity related to urological quality of life (UQL=CVU) was tolerable in 75% and unsatisfactory in 25%. Urinary retention was present in 6.9%. IPSS, V100 and D90 were related to the urinary toxicity grade. Rectal toxicity (RTOG) G2 was 0.6%. Sexual potency showed no changes with regard to the basal in 69%. Actuarial biochemical control was 89.8% at four years.
Conclusions
Brachytherapy with 125-I seeds yields acceptable toxicity and excellent biochemical control.
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Morillo, V., Guinot, J.L., Tortajada, I. et al. Secondary effects and biochemical control in patients with early prostate cancer treated with 125-I seeds. Clin Transl Oncol 10, 359–366 (2008). https://doi.org/10.1007/s12094-008-0212-y
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DOI: https://doi.org/10.1007/s12094-008-0212-y