Robotic Athermal Nerve-Sparing Radical Prostatectomy

Case Comprehensive Cancer Center (Case CCC)

Status: Withdrawn

Conditions: Stage I Prostate Cancer; Stage IIA Prostate Cancer

Treatments: Other: laboratory biomarker analysis; Other: questionnaire administration; Other: quality-of-life assessment; Procedure: robot-assisted laparoscopic surgery

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT02079155

CASE12811 (Other Identifier)

P30CA043703 (U.S. NIH Grant/Contract)

NCI-2014-00393 (Registry Identifier)

Details and patient eligibility

About

This randomized clinical trial compares a recently developed technique, called robotic laparoendoscopic single-site radical prostatectomy (R-LESS RP), to the current standard of robotic technique for prostate cancer, robot-assisted laparoscopic prostatectomy (RALP) in treating patients with newly diagnosed, locally confined prostate cancer. Both procedures are types of robotic radical prostatectomy, or the robot-assisted removal of the prostate though a small incision in the belly. In the standard approach, 4-5 small (1-2 cm) incisions are made in the lower abdomen to allow the insertion of robotic instruments. In the R-LESS technique, all instruments are inserted through a single incision. R-LESS RP is less invasive than RALP and may leave a smaller scar and cause less pain.

Full description

PRIMARY OBJECTIVES:

I. To evaluate pain and analgesic requirement of R-LESS RP compared to standard RALP.

SECONDARY OBJECTIVES:

I. Time to oral intake. II. Time to resume ambulation. III. Hospital stay, counted in whole days from the day of surgery to the day of discharge.

IV. Perioperative parameters, including: operative time (defined as time elapsed from skin incision to placement of the final skin suture); estimated blood loss; additional ports; conversion to standard RALP (in R-LESS RP patients), or laparoscopic, or open surgery; length of stay.

V. Intraoperative complications. VI. Postoperative complications, recorded according to the Clavien classification.

VII. Body image perception, measured using the body image questionnaire (BIQ). VIII. Scar evaluation (at suture removal and at 6 month) by using a validated assessment tool, the Patient and Observer Scar Assessment Scale.

IX. Health related quality of life, measured as patients' perception of functioning, disability, and well-being related to the following eight concepts: physical functioning, role limitations caused by physical health problems, bodily pain, general health, vitality, social functioning, role limitation caused by emotional problems, and mental health.

X. Urinary continence, assessing the number of pads used daily. XI. Erectile Function, assessed by the International Index of Erectile Function (IIEF-5).

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients undergo standard RALP.

ARM II: Patients undergo R-LESS RP.

After completion of study treatment, patients are followed up periodically for 1 year.

Sex: Male

Ages: 35 to 72 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients must have a biopsy proven newly diagnosed locally confined, stage T1a, T2a or T2b prostate cancer
• Judged by the study doctor to be a suitable candidate for a radical prostatectomy
• Serum prostate specific antigen equal to or less than 10 ng/mL
• Gleason score equal to or less than 7
• Life expectancy greater than 10 years
• Prostate size on trans-rectal ultrasound (TRUS) measurement less than 50 grams
• Favorable operative risk defined as American Society of Anesthesiology Score (ASA score) =< 3
• Ability to understand and the willingness to sign a written informed consent document or have a surrogate with the ability to understand and the willingness to sign a written informed consent

Exclusion criteria

• Patients with any prior pelvic surgery
• Patients with prior history of pelvic fractures or hip replacement
• Large pelvic or intra-abdominal masses
• Any condition or history of illness or surgery that, in the opinion of the investigator, might confound the results of the study or pose additional risk to the patient (e.g. significant cardiovascular conditions)
• Poor surgical risk (defined as American Society of Anesthesiology Score > 3)
• Active infection
• Uncorrected coagulopathy
• Body mass index equal to or greater than 35

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Arm I (RALP)

Active Comparator group

Description:

Patients undergo standard RALP.

Treatment:

Other: quality-of-life assessment

Procedure: robot-assisted laparoscopic surgery

Procedure: robot-assisted laparoscopic surgery

Other: questionnaire administration

Other: laboratory biomarker analysis

Arm II (R-LESS RP)

Experimental group

Description:

Patients undergo R-LESS RP.

Treatment:

Other: quality-of-life assessment

Procedure: robot-assisted laparoscopic surgery

Procedure: robot-assisted laparoscopic surgery

Other: questionnaire administration

Other: laboratory biomarker analysis