About this trial
BALANCE is a multicenter, prospective, randomized controlled trial enrolling men with unilateral high-risk localized prostate cancer identified by prostate biopsy, multiparametric MRI, and PSMA PET imaging. Eligible patients scheduled for robot-assisted radical prostatectomy will be randomized in a 1:1 ratio to undergo either unilateral extended pelvic lymph node dissection or bilateral extended pelvic lymph node dissection.
Pelvic lymph node dissection is commonly performed in high-risk prostate cancer for staging purposes, but its therapeutic benefit remains uncertain and the procedure may increase operative time, costs, and postoperative morbidity. Modern imaging techniques may improve the identification of patients with predominantly unilateral disease and support a more selective surgical approach.
The co-primary objectives are to compare 3-year biochemical recurrence-free survival and early postoperative PSA persistence between the two surgical strategies. Secondary objectives include comparison of perioperative complications, operative time, blood loss, length of hospital stay, quality of life, long-term oncologic outcomes, and costs.
This study is designed to determine whether unilateral extended pelvic lymph node dissection can reduce surgical morbidity while preserving oncologic outcomes in appropriately selected patients with high-risk prostate cancer.
Eligibility criteria
Qualifiers
Male patients aged 18 years or older
Histologically confirmed unilateral high-risk localized prostate cancer, defined by at least one of the following: ISUP Grade Group 4 or 5; suspicion of at least cT3a disease on multiparametric MRI and/or PSMA PET; or PSA greater than or equal to 20 ng/mL with a unilateral index lesion
Unilateral features of the index lesion defined by biopsy, multiparametric MRI, and PSMA PET
No PSMA PET-positive pelvic lymph nodes contralateral to the dominant side of the prostate cancer
Disqualifiers
Any prostate cancer treatment prior to prostatectomy, including androgen deprivation therapy, neoadjuvant chemotherapy, radiotherapy, or focal ablative therapy
Prior active treatment for prostate cancer
Contralateral ISUP Grade Group 4 to 5 prostate cancer
Contralateral ISUP Grade Group 2 in more than 4 positive cores or ISUP Grade Group 3 in more than 2 positive cores
Trial design
Treatments tested in this trial
- Unilateral Extended Pelvic Lymph Node Dissection
- Bilateral Extended Pelvic Lymph Node Dissection
Treatment groups
Sponsors and collaborators
University of Turin, Italy
Lead sponsor
AIRC (Italian Association for Cancer Research)
Collaborator
Fondazione Ricerca Molinette
Collaborator