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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
820
Extended pelvic lymph node dissection performed only on the side of the dominant lesion, as defined by biopsy, multiparametric MRI, and PSMA PET findings.
Extended pelvic lymph node dissection performed bilaterally according to the study surgical template during robot-assisted radical prostatectomy.
Humanitas Clinical and Research Centre & Humanitas University
Rozzano, Milano, Italy
NOT_YET_RECRUITINGIRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico di Sant'Orsola-Malpighi & University of Bologna
Bologna, Italy
NOT_YET_RECRUITINGUniversità degli Studi di Firenze / AOU Careggi
Florence, Italy
NOT_YET_RECRUITINGUniversità degli Studi di Foggia / AO Ospedali Riuniti di Foggia
Foggia, Italy
NOT_YET_RECRUITINGIRCCS Ospedale Policlinico San Martino & University of Genoa
Genova, Italy
NOT_YET_RECRUITINGIEO, Istituto Europeo di Oncologia
Milan, Italy
NOT_YET_RECRUITINGASST Grande Ospedale Metropolitano Niguarda
Milan, Italy
NOT_YET_RECRUITINGUniversità degli Studi di Modena / AOU Modena
Modena, Italy
NOT_YET_RECRUITINGIstituto Nazionale Tumori, IRCCS, Fondazione "G. Pascale"
Naples, Italy
NOT_YET_RECRUITINGUniversità Tor Vergata / Policlinico Tor Vergata
Roma, Italy
NOT_YET_RECRUITING...and 4 more locations
Biochemical Recurrence-Free Survival
Biochemical recurrence defined as postoperative PSA greater than 0.1 ng/mL with three consecutive rises or initiation of prostate cancer-specific secondary treatment more than 6 months after surgery
Time frame: 3 years after surgery
PSA Persistence
Postoperative PSA greater than 0.1 ng/mL at 6 weeks after surgery confirmed by an additional PSA measurement performed 2 weeks later.
Time frame: 8 weeks after surgery
Perioperative Complications
Complications graded using the Clavien-Dindo classification and assessed for likelihood of being related to pelvic lymph node dissection.
Time frame: Up to 6 months after surgery
Operative Time
Total operative time recorded during robot-assisted radical prostatectomy and pelvic lymph node dissection.
Time frame: During surgery
Estimated Blood Loss
Intraoperative estimated blood loss.
Time frame: During surgery
Length of Hospital Stay
Number of days from surgery to discharge from the index hospitalization.
Time frame: During the index hospitalization, up to 90 days after surgery
Overall Prostate Cancer Quality of Life Score Assessed Using the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP)
Overall prostate cancer-related quality of life assessed using the Expanded Prostate Cancer Index Composite for Clinical Practice questionnaire. The overall score is calculated by summing the five domain summary scores: urinary incontinence, urinary irritation/obstruction, bowel, sexual, and vitality/hormonal. Total scores range from 0 to 60, with higher scores indicating worse symptoms and poorer quality of life.
Time frame: 1 year after surgery
Treatment-Free Survival
Absence of any salvage local or systemic treatment after surgery.
Time frame: 3 years after surgery
Systemic Treatment-Free Survival
Absence of systemic treatment after surgery.
Time frame: 3 years after surgery
Metastasis-Free Survival
Absence of metastatic disease during follow-up, including PSMA PET assessment when clinically indicated after multidisciplinary discussion.
Time frame: 3 years after surgery
Cost-Effectiveness
Cost-effectiveness assessed as incremental cost per quality-adjusted life year at 1 year after surgery.
Time frame: 1 year after surgery
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