Open Vs Robotic-Assisted Radical Cystectomy: A Randomized Trial
Primary Purpose
Bladder Cancer Requiring Cystectomy
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Open radical cystectomy
Robotic assisted radical cystectomy
DaVinci robot
Sponsored by
About this trial
This is an interventional treatment trial for Bladder Cancer Requiring Cystectomy focused on measuring open cystectomy, robotic assisted radical cystectomy, bladder cancer
Eligibility Criteria
Inclusion Criteria:
- Patient must have biopsy proven bladder cancer. Official pathology report reviewed at the participating institution is required.
- Bladder cancer must be clinical stage T1-T4, N0-1, M0. (AJCC 7th edition) or refractory cis (carcinoma in situ).
Exclusion Criteria:
- Inability to give informed consent.
- Prior major abdominal and pelvic open surgical procedures that would preclude a safe robotic approach, as determined by the treating surgeon.
- At the discretion of the treating surgeon, any pre-existing condition such as severe chronic obstructive pulmonary disease that precludes a safe initiation or maintenance of pneumoperitoneum over a prolonged period of time and during surgery.
- Age <18 or >99 years.
- Pregnancy.
Sites / Locations
- Mayo Clinic Arizona
- University of California, Irvine Medical Center (UC Irvine)
- Stanford University
- University of Miami
- University of Chicago Medical Center
- Loyola University Medical Center
- Brigham and Women's Hospital
- University of Michigan Health System
- University of Minnesota
- Mayo Clinic
- University of North Carolina
- Ohio State University Medical Center
- Vanderbilt University Medical Center
- The University of Texas Health Science Center at San Antonio, Medical Arts & Research Center
- University of Virginia Health Science Center, Department of Urology
- Cancer Research and Biostatistics (Data Management and Statistical Office)
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Open cystectomy
Robotic assisted radical cystectomy
Arm Description
Open cystectomy performed using an incision made just above or at the level of umbilicus to the pubic symphysis.
Robotic assisted Radical Cystectomy (RARC) is accomplished by a robot assisted laparoscopic approach.
Outcomes
Primary Outcome Measures
Percentage of Participants With 2-year Progression Free Survival (PFS)
Progression will be determined by the treating physician using the Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 criteria based on radiographic or pathological evidence of disease progression or death from disease.
Number of Participants With Positive Margins
Evaluated are the number of participants with positive surgical, bladder, and urethral margins. Positive margin is defined as presence of tumor cells at the edge of the dissected tissue.
Number of Participants Requiring Lymph Node Dissection
Evaluated are the number of participants requiring extended or standard lymph node dissection
Quality of Life (QOL) Outcomes
Functional Assessment of Cancer Therapy- Vanderbilt Cystectomy Index (FACT-VCI) scores range is 0-168 which is sum of physical, emotional, wellbeing, and FACTS Bl Cys. higher scores=better QOL.
Number of Participants With Post-surgical Complications
Post surgical complications will be evaluated using the Clavien grading system with scores ranging from 0-5 with the higher number indicating increased post-surgical complications.
Amount of Estimated Blood Loss (EBL) in ml
Perioperative measures such as EBL will be evaluated by measuring the amount of participant blood loss in ml.
Number of Participants Requiring Blood Transfusion
Number of participants requiring peri, intra, and post operative blood transfusion.
Number of Days of Post Operative Length of Hospital Stay
Number of days of post operative length of hospital stay will be evaluated
Length of Operative Time
Length of minutes of cystectomy procedure
Laboratory Values
Serum Hemoglobin (Hb) and Albumin will be reported in grams per deciliters (g/dL)
Measures of Functional Independence as Assessed by the Activities of Daily Living (ADL) Questionnaire
Participant reported ADL questionnaire is a 7 item questionnaire with scores ranging from 7-21 with a lower score indicating increased independence.
Percentage of Participants With 3-year Progression Free Survival (PFS)
Progression will be determined by the treating physician using the RECIST Version 1.1 criteria based on radiographic or pathological evidence of disease progression or death from disease.
Quality of Life (QOL) Outcomes as Assessed by the Short Form 8 (SF-8) Questionnaire
The SF-8 consists of two component summary scores; physical (PCS) and mental component summary (MCS). They are scored by weighting each score to a norm-based scoring model. The total scores will be reported as a percentile with higher score indicating better quality of health.
Total Number of Participants Requiring Intra-operative Fluid Requirement
Total number of participants requiring Intra-operative fluid requirement. (blood+plasma+platelets) Note: In robotic group 1 participant received both plasma and platelets and 1 other received platelets in addition to blood transfusion. In the open group 5 participants received plasma in addition to blood transfusion.
Total Postoperative Analgesic Requirements
Total postoperative analgesic requirements in milli grams
Creatinine Value.
Serum creatinine will be reported in milligrams per deciliters (mg/dL).
Measures of Functional Independence as Assessed by the Instrumental Activities of Daily Living (IADL) Questionnaire
Participant reported IADL questionnaire is an 8 item questionnaire with scores ranging from 8-32 with a lower score indicating increased independence.
Performance Related Measures of Functional Independence as Assessed by the Hand Grip Strength Test
The hand grip strength test is measured in kilograms of pressure using a handheld dynamometer.
Performance Related Measures of Functional Independence as Assessed by the Time Up and Go (TUG) Walking Test
The TUG test is measured in seconds. Patients will be timed as they rise from a standard chair, walk 3 meters, turn, walk back, and sit again.
Quality of Life (QOL) Outcomes as Assessed by the Functional Assessment of Cancer Therapy - Vanderbilt Cystectomy Index (FACT-VCI) Questionnaire
FACT-VCI consists of eight domains: Five subscale scores (physical wellbeing, social wellbeing, emotional wellbeing, functional wellbeing, and FACT for patients with Bladder Cancer following Cystectomy [FACT-BL-Cys]) and three derived scores (trial outcome index), FACT-General form (FACT-G), and FACT-BL-Cys Total.The ranges of scores for each domain are as follows: 0-28 for physical, social, and functional wellbeing; 0-24 for emotional wellbeing; 0-60 for FACT-BL-Cys; 0-116 for FACT-VCI Trial Outcome Index (sum of physical wellbeing, functional wellbeing, and FACT-BL-Cys scores); 0-108 for FACT-G (sum of physical, social, emotional, and functional wellbeing scores); and 0-168 for FACT-BL-Cys Total (sum of physical, social, emotional, and functional wellbeing scores, and FACT-BL-Cys).The higher score indicates increased wellbeing.
Secondary Outcome Measures
Cost
Fixed and variable costs associated with the procedure.
Full Information
NCT ID
NCT01157676
First Posted
June 30, 2010
Last Updated
October 30, 2020
Sponsor
University of Miami
Collaborators
National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT01157676
Brief Title
Open Vs Robotic-Assisted Radical Cystectomy: A Randomized Trial
Official Title
Open Vs Robotic-Assisted Radical Cystectomy: A Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Miami
Collaborators
National Cancer Institute (NCI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a multi-institutional, randomized trial evaluating oncologic, perioperative, and functional outcomes following two standard care procedures for radical cystectomy. The participants will have one of the standard care procedures as part of their care. The two procedures that will be followed are open radical cystectomy and robotic assisted radical cystectomy (RARC). Open cystectomy is considered to be the more traditional approach. While newer, RARC is considered to be equivalent to open surgery when it is performed by a trained robotics surgeon. The reported complication rates of RARC appear comparable to open surgery. This means there is no significant difference in the risk between the two standard procedures. However, despite these potential advantages, true comparison between the open and robotic technique with regards to long term cancer related and functional outcomes has not been accomplished because previous studies did not compare patients of equal health status. The researchers hope to learn whether or not patients undergoing RARC recover more quickly than or at the same rate as patients undergoing an open radical cystectomy while having non inferior cancer related outcomes. This study is funded by the National Institutes of Health (NIH).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer Requiring Cystectomy
Keywords
open cystectomy, robotic assisted radical cystectomy, bladder cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Non inferiority phase 3 randomized clinical trial comparing robotic to open radical cystectomy
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Open cystectomy
Arm Type
Active Comparator
Arm Description
Open cystectomy performed using an incision made just above or at the level of umbilicus to the pubic symphysis.
Arm Title
Robotic assisted radical cystectomy
Arm Type
Active Comparator
Arm Description
Robotic assisted Radical Cystectomy (RARC) is accomplished by a robot assisted laparoscopic approach.
Intervention Type
Procedure
Intervention Name(s)
Open radical cystectomy
Intervention Description
Standard of care removal of urinary bladder.
Intervention Type
Procedure
Intervention Name(s)
Robotic assisted radical cystectomy
Intervention Description
Standard of care removal of urinary bladder using DaVinci robot.
Intervention Type
Device
Intervention Name(s)
DaVinci robot
Intervention Description
DaVinci robotic surgical system.
Primary Outcome Measure Information:
Title
Percentage of Participants With 2-year Progression Free Survival (PFS)
Description
Progression will be determined by the treating physician using the Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 criteria based on radiographic or pathological evidence of disease progression or death from disease.
Time Frame
24 months
Title
Number of Participants With Positive Margins
Description
Evaluated are the number of participants with positive surgical, bladder, and urethral margins. Positive margin is defined as presence of tumor cells at the edge of the dissected tissue.
Time Frame
At time of cystectomy, approximately 1 hour.
Title
Number of Participants Requiring Lymph Node Dissection
Description
Evaluated are the number of participants requiring extended or standard lymph node dissection
Time Frame
At time of cystectomy, approximately 1 hour
Title
Quality of Life (QOL) Outcomes
Description
Functional Assessment of Cancer Therapy- Vanderbilt Cystectomy Index (FACT-VCI) scores range is 0-168 which is sum of physical, emotional, wellbeing, and FACTS Bl Cys. higher scores=better QOL.
Time Frame
at baseline, 3 month, and 6 months
Title
Number of Participants With Post-surgical Complications
Description
Post surgical complications will be evaluated using the Clavien grading system with scores ranging from 0-5 with the higher number indicating increased post-surgical complications.
Time Frame
90 days post operative
Title
Amount of Estimated Blood Loss (EBL) in ml
Description
Perioperative measures such as EBL will be evaluated by measuring the amount of participant blood loss in ml.
Time Frame
At time of cystectomy, approximately 1 hour
Title
Number of Participants Requiring Blood Transfusion
Description
Number of participants requiring peri, intra, and post operative blood transfusion.
Time Frame
At time of cystectomy, approximately 1 hour
Title
Number of Days of Post Operative Length of Hospital Stay
Description
Number of days of post operative length of hospital stay will be evaluated
Time Frame
Day 10 post surgery
Title
Length of Operative Time
Description
Length of minutes of cystectomy procedure
Time Frame
At time of cystectomy, approximately 1 hour
Title
Laboratory Values
Description
Serum Hemoglobin (Hb) and Albumin will be reported in grams per deciliters (g/dL)
Time Frame
baseline, 6 weeks, 3 months, 6 months, 12 months, 24 months, 36 months
Title
Measures of Functional Independence as Assessed by the Activities of Daily Living (ADL) Questionnaire
Description
Participant reported ADL questionnaire is a 7 item questionnaire with scores ranging from 7-21 with a lower score indicating increased independence.
Time Frame
baseline, 1 month , 3 months, 6 months
Title
Percentage of Participants With 3-year Progression Free Survival (PFS)
Description
Progression will be determined by the treating physician using the RECIST Version 1.1 criteria based on radiographic or pathological evidence of disease progression or death from disease.
Time Frame
3 years
Title
Quality of Life (QOL) Outcomes as Assessed by the Short Form 8 (SF-8) Questionnaire
Description
The SF-8 consists of two component summary scores; physical (PCS) and mental component summary (MCS). They are scored by weighting each score to a norm-based scoring model. The total scores will be reported as a percentile with higher score indicating better quality of health.
Time Frame
baseline, 3 month, and 6 month
Title
Total Number of Participants Requiring Intra-operative Fluid Requirement
Description
Total number of participants requiring Intra-operative fluid requirement. (blood+plasma+platelets) Note: In robotic group 1 participant received both plasma and platelets and 1 other received platelets in addition to blood transfusion. In the open group 5 participants received plasma in addition to blood transfusion.
Time Frame
At time of cystectomy, approximately 1 hour
Title
Total Postoperative Analgesic Requirements
Description
Total postoperative analgesic requirements in milli grams
Time Frame
At time of cystectomy, approximately 1 hour
Title
Creatinine Value.
Description
Serum creatinine will be reported in milligrams per deciliters (mg/dL).
Time Frame
baseline, 6 weeks, 3 months, 6 months, 12 months, 24 months, 36 months
Title
Measures of Functional Independence as Assessed by the Instrumental Activities of Daily Living (IADL) Questionnaire
Description
Participant reported IADL questionnaire is an 8 item questionnaire with scores ranging from 8-32 with a lower score indicating increased independence.
Time Frame
baseline, 1 month, 3 months, 6 months
Title
Performance Related Measures of Functional Independence as Assessed by the Hand Grip Strength Test
Description
The hand grip strength test is measured in kilograms of pressure using a handheld dynamometer.
Time Frame
baseline, 1 month, 3 months, 6 months
Title
Performance Related Measures of Functional Independence as Assessed by the Time Up and Go (TUG) Walking Test
Description
The TUG test is measured in seconds. Patients will be timed as they rise from a standard chair, walk 3 meters, turn, walk back, and sit again.
Time Frame
baseline, 1 month, 3 months, 6 months
Title
Quality of Life (QOL) Outcomes as Assessed by the Functional Assessment of Cancer Therapy - Vanderbilt Cystectomy Index (FACT-VCI) Questionnaire
Description
FACT-VCI consists of eight domains: Five subscale scores (physical wellbeing, social wellbeing, emotional wellbeing, functional wellbeing, and FACT for patients with Bladder Cancer following Cystectomy [FACT-BL-Cys]) and three derived scores (trial outcome index), FACT-General form (FACT-G), and FACT-BL-Cys Total.The ranges of scores for each domain are as follows: 0-28 for physical, social, and functional wellbeing; 0-24 for emotional wellbeing; 0-60 for FACT-BL-Cys; 0-116 for FACT-VCI Trial Outcome Index (sum of physical wellbeing, functional wellbeing, and FACT-BL-Cys scores); 0-108 for FACT-G (sum of physical, social, emotional, and functional wellbeing scores); and 0-168 for FACT-BL-Cys Total (sum of physical, social, emotional, and functional wellbeing scores, and FACT-BL-Cys).The higher score indicates increased wellbeing.
Time Frame
baseline, 3 months, 6 months
Secondary Outcome Measure Information:
Title
Cost
Description
Fixed and variable costs associated with the procedure.
Time Frame
Day 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient must have biopsy proven bladder cancer. Official pathology report reviewed at the participating institution is required.
Bladder cancer must be clinical stage T1-T4, N0-1, M0. (AJCC 7th edition) or refractory cis (carcinoma in situ).
Exclusion Criteria:
Inability to give informed consent.
Prior major abdominal and pelvic open surgical procedures that would preclude a safe robotic approach, as determined by the treating surgeon.
At the discretion of the treating surgeon, any pre-existing condition such as severe chronic obstructive pulmonary disease that precludes a safe initiation or maintenance of pneumoperitoneum over a prolonged period of time and during surgery.
Age <18 or >99 years.
Pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dipen J Parekh, MD
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Arizona
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85054
Country
United States
Facility Name
University of California, Irvine Medical Center (UC Irvine)
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Stanford University
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
University of Chicago Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Loyola University Medical Center
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
University of Michigan Health System
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
Ohio State University Medical Center
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Vanderbilt University Medical Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
Facility Name
The University of Texas Health Science Center at San Antonio, Medical Arts & Research Center
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
University of Virginia Health Science Center, Department of Urology
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Facility Name
Cancer Research and Biostatistics (Data Management and Statistical Office)
City
Seattle
State/Province
Washington
ZIP/Postal Code
98101
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
35171260
Citation
Venkatramani V, Reis IM, Gonzalgo ML, Castle EP, Woods ME, Svatek RS, Weizer AZ, Konety BR, Tollefson M, Krupski TL, Smith ND, Shabsigh A, Barocas DA, Quek ML, Dash A, Parekh DJ. Comparison of Robot-Assisted and Open Radical Cystectomy in Recovery of Patient-Reported and Performance-Related Measures of Independence: A Secondary Analysis of a Randomized Clinical Trial. JAMA Netw Open. 2022 Feb 1;5(2):e2148329. doi: 10.1001/jamanetworkopen.2021.48329.
Results Reference
derived
PubMed Identifier
29976469
Citation
Parekh DJ, Reis IM, Castle EP, Gonzalgo ML, Woods ME, Svatek RS, Weizer AZ, Konety BR, Tollefson M, Krupski TL, Smith ND, Shabsigh A, Barocas DA, Quek ML, Dash A, Kibel AS, Shemanski L, Pruthi RS, Montgomery JS, Weight CJ, Sharp DS, Chang SS, Cookson MS, Gupta GN, Gorbonos A, Uchio EM, Skinner E, Venkatramani V, Soodana-Prakash N, Kendrick K, Smith JA Jr, Thompson IM. Robot-assisted radical cystectomy versus open radical cystectomy in patients with bladder cancer (RAZOR): an open-label, randomised, phase 3, non-inferiority trial. Lancet. 2018 Jun 23;391(10139):2525-2536. doi: 10.1016/S0140-6736(18)30996-6.
Results Reference
derived
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Open Vs Robotic-Assisted Radical Cystectomy: A Randomized Trial
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