Prostate cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with non-metastatic prostate cancer who, after receiving a thorough explanation of treatment options from their attending physician, have chosen either HIFU or RARP; and patients diagnosed with benign prostatic hyperplasia who, after receiving a thorough explanation of treatment options from their attending physician, have chosen TUR-P. 2. Individuals with a PSA level below 20 ng/mL. 3. Individuals who, after receiving sufficient explanation regarding participation in this study, have provided written informed consent of their own free will.
Exclusion criteria
Exclusion criteria: 1. Individuals receiving hormonal therapy. 2. Individuals from whom informed consent could not be obtained. 3. Other individuals deemed inappropriate for the study by the principal investigator or sub-investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Temporal changes in antitumor immune responses before and after each treatment modality | — |
Countries
Japan
Contacts
Tokai University Hospital Department of Urology