A Trial Evaluating Toxicity of SBRT and LDRB in Localized Prostate Cancer.

Prior treatment

• Prior radical surgery for carcinoma of the prostate, or prior TURP (Trans-Urethral Resection of the Prostate).
• Prior pelvic radiotherapy or prior radiotherapy that would result in overlap of radiation fields.
• Prior chemotherapy for prostate cancer, or prior chemotherapy within the last 3 years.
• Prior cryosurgery of the prostate.
• Prior or current bleeding diathesis making fiducial placement or brachytherapy procedure unsafe.
• Previous androgen deprivation therapy within 6 months of the registration.

Other illness

• Clinical or radiological evidence of metastatic disease or nodal involvement.

Lab values

• Any severe active comorbidity, laboratory abnormality, psychiatric illnesses, active or uncontrolled infections, serious illnesses or medical conditions that would prevent the patient from participating or to be managed according to the protocol (according to investigator's decision). Such examples includes active inflammatory bowel disease, significant urinary symptoms,

Age

• Patients with a history of other malignancies, except: adequately treated non-melanoma skin cancer, or other solid tumors curatively treated with no evidence of disease for ≥ 3 years.

Other

• Clinical stage ≥ T2b.
• Gleason score ≥ 4 + 3.
• Bilateral hip prostheses

• Histologically confirmed adenocarcinoma of the prostate diagnosed within the last 8 months. Patients on active surveillance with evidence of disease progression are eligible to the protocol as long as they meet the eligibility criteria and have a recent prostate biopsy (within 8 months).
• Low-risk and favourable intermediate-risk prostate cancer patients are eligible according to the following definitions:
  • Low-risk disease defined as: Clinical stage T1-T2a and Gleason 6 and PSA ≤ 10 ng/mL
  • Favourable intermediate-risk cancer defined by a single NCCN intermediate risk factor:
  • \[NCCN : National Comprehensive Cancer Network\]
• Clinical stage T2b
• PSA \> 10 but ≤ 20 ng/mL
• Gleason 7 (3+4)
  • Lymph node evaluation by either computed tomography (CT) or magnetic resonance imaging (MRI) is optional and is left at the discretion of the treating physician.
• Age ≥ 18 years
• Eastern Cooperative Oncology Group performance status 0-1
• Patient considered medically fit for LDR brachytherapy
• Prostate volume ≤ 60 cc, measured by Trans-Rectal UltraSound (TRUS), CT or MRI, within the last 6 months.
• International Prostate Symptom Score (IPSS) ≤ 20 (alpha blockers allowed)
• No alpha reductase inhibitors use within two weeks of randomization
• No hormonal therapy is accepted
• Patients must provide a study-specified informed consent form prior to study entry.
• Patients must be willing and able to complete the EPIC-26, IPSS and SHIM questionnaires.
  • \[EPIC-26: Expanded Prostate Cancer Index Composite score ; SHIM: Sexual Health Inventory for Men questionnaire\].