Salvage brachytherapy for local recurrences of prostate cancer treated earlier with radiotherapy

Purpose: Radiation therapy for localized prostate cancer is a standard option of treatment. Local recurrences (biochemical and clinical) occurred in about 50% (depending on the initial stage and other prognostic factors). Usually local recurrences have ominous prognosis. The standard treatment is hormonotherapy.
Material and methods: In MSC Memorial Cancer Center and Institute of Oncology, Gliwice Branch, a researched program on salvage HDR brachytherapy for local recurrences of prostate cancer treated earlier with radiotherapy has been opened since February 2008. Eligibility criteria: confirmed local recurrence after treatment for localized prostate cancer at east 2 years ago (transrectal ultrasound or MRI of the prostate, bone scan for occult metastases, biopsy of the prostate for histopatological confirmation of the recurrences). The earlier treatment were mainly external beam radiation but patients treated with external bean radiation with boost from brachytherapy are not excluded. Exclusion criteria was the same as for any HDR brachytherapy of prostate (volume > 60 cm³, TURP within 6 months, infiltration of the external sphincter of the bladder neck, significant urinary obstructive symptoms, pubic arch interference, litotomy position or anesthesia not possible). HDR brachytherapy was delivered using an Iridium-192 stepping source (MicroSelectron™, Nucletron NV). Treatment planning was performed intra-opertively. Needle applications were performed during spinal anesthesia. The treatment consisted of 3 fraction 10 Gy each given every 14 days. The dose was specificated on the prostate capsule or 2-3 mm from it (depending on clinical case). Generally homogenous needle distributions were applied with planed hot-spot in case of visible tumor. Maximal urethral doses (calculated at the centre of each urethral outline each 5 mm) were constrained to be 120% of prescribed dose. Maximal bladder and rectum doses were constrained to be 70% of prescribed dose.
Results: Fifteen patients eligible were treated and analyzed from February 2008. All patients completed the treatment without major complication. The most common early complication were: macroscopic hematuria, pain in lower part of the abdomen, transient dysuria. During the first week after the procedure transient increase in IPPS score were noticed. A Foley catheter was removed on day 2nd to 5th. No complication after spinal anesthesia were observed. Acute...


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