Patients with prostate cancer who received luteinizing hormone-releasing hormone (LH-RH) agonist, had biochemical progression
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient with prostate cancer defined by pathological examination 2. Patient with first biochemical failure during hormone therapy 3. Patient age above 20 years or older 4. Performance status grade 0, 1 or 2 5. Chemical laboratory values met predefined criteria
Exclusion criteria
Exclusion criteria: 1. Serum teststerone level above 0.5ng/ml 2. Patient with clinical symptom, bone pain or urinary retention at PSA failure 3. Patient with the treatment history, who was administered both goserelin and leuprolide 4. Patient administered anti-androgen drug as CAB 5. Administeration of estrogen 6. Sytemic administeration of corticosteroid 7. Patient received chemotherapy 8. Patient with severe diabetes 9. Patients with severe psychosis 10. Patients with double cancer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The percent prostate specific antigen change after switching luteinizing hormone-releasing hormone agonist therapy at 3 and 6 months | — |
Countries
Japan
Contacts
Kawasaki Medical School Department of Urology