search
Back to results

Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers

Primary Purpose

Locally Advanced Pelvic Cancer That Require Pelvic Exenteration

Status
Recruiting
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
robot-assisted total pelvic exenteration
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Locally Advanced Pelvic Cancer That Require Pelvic Exenteration focused on measuring robot-assisted, pelvic exenteration, minimally invasive surgery, locally advanced rectal and sigmoid cancers, localized central pelvic recurrence of cervical cancer or endometrial cancers, feasibility

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients (>18 years)
  • locally advanced pelvic cancer that require pelvic exenteration
  • eligible for robot- assisted minimally invasive surgery by the respective multidisciplinary teams, may be included in the study.

Exclusion Criteria:

  • Any reason why the patient in the investigator's opinion is not suited for inclusion.

Sites / Locations

  • Oslo University Hospital The Radium HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Locally advanced pelvic cancer that requires total pelvic exenteration

Arm Description

Adult patients (>18 years) with locally advanced pelvic cancer that require pelvic exenteration considered eligible for robot- assisted minimally invasive surgery by the respective multidisciplinary teams

Outcomes

Primary Outcome Measures

Rate of R0 resection
R0 resection in oncological surgery means resection with circumferential margin >1mm from the tumour. R0 resection is considered as an important predictor for outcome.

Secondary Outcome Measures

Rate of conversion from laparoscopic robot-assisted to open surgery
a quality indicator and feasibility measure for the procedure
Rate and type of postoperative complications
Any complications within the first 90 days after surgery
Hospital length of stay
How long the patient stay in Hospital after surgery
Disease free survival
If the patient have any recurrent disease
Overall survival
If the patient is alive
Quality of Life measured with the validated EORTC Quality of Life Questionnaire C-30 measurement tool (QoL C-30)
Quality of Life measured before and on specific controles postoperative

Full Information

First Posted
November 26, 2021
Last Updated
March 31, 2023
Sponsor
Oslo University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT05186493
Brief Title
Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers
Official Title
Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2021 (Actual)
Primary Completion Date
December 1, 2025 (Anticipated)
Study Completion Date
December 1, 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Radium Hospital Oslo University Hospital Estimated date of first patient enrolled: 3rd quarter 2021 Anticipated recruitment period: 4 years Estimated date of last patient completed: 4th quarter 2025 Locally advanced pelvic cancer that requires total pelvic exenteration Expected study-specific follow-up period per patient: 5 years according to standard follow-up for this patient group Primary endpoint: R0 resection rate (circumferential resection margin >1mm) Secondary endpoints: Rate of conversion to open surgery, peri- and postoperative complications, hospital length of stay, wound healing at 3 months follow-up, Quality of Life measured by EORTC Quality of Life Questionnaire C-30 preoperatively, at 3 months and 3 year follow-ups, disease-free survival, overall survival. Diagnosis specific endpoints. Open label observational study.
Detailed Description
Pelvic exenteration for locally advanced rectal cancer (LARC) and locally advanced sigmoid cancer LARC includes tumours threatening the mesorectal fascia or invading adjacent organs and structures (9). Locally advanced sigmoid cancer is defined as tumors extending through the colon wall with perforation and/or invasion of adjacent organs or structures (10). Surgical removal is the standard curative approach for these tumours, and achievement of complete tumour removal, or R0 resection, is prognostically important. The Residual tumour (R) classification defines R0 resection as having > 1 mm margin between the tumour and surrounding normal tissue, R1 resection as ≤ 1 mm margin, and R2 as local macroscopic residual tumour after resection (11). If R0 resection is achieved, the outcome for the patient is dramatically superior compared to when resection is incomplete. In a large study of 1291 LARC cases, the overall survival was 43 months in R0 cases compared to 21 months if R1 resection was achieved (12). Neoadjuvant therapy including chemotherapy and (chemo) radiotherapy ((C) RT) has resulted in improved local control (13), presumably by increasing the rate of complete surgical tumour removal (14), when the patient is operated. Total radiation dose towards the pelvis are usually 25-50 Gy, often with concomitant fluoropyrimidine-based chemotherapy. Although the neoadjuvant radiotherapy improves prognosis (14), it also imposes challenges. The surgery itself might be difficult because of edema and fibrosis resulting in potentially involved margins, and the healing after surgery is impaired leading to increased postoperative morbidity. This holds true for all tumours in the pelvis that receive radiotherapy before surgery. Despite neoadjuvant therapy, tumours still often require resection of neighboring organs in order to achieve R0-resection. First described in 1948, total pelvic exenteration can be defined as the removal of the bladder, removal of the prostate (in males), removal of the uterus or the vaginal vault and partial or total resection of the vagina (in females), and the removal of the rectum with or without the anus (15). Total pelvic exenteration is extensive surgery with reconstructions that include two stomas. Locally advanced rectal cancers and locally advanced sigmoid cancers with multiorgan involvement e.g. rectal cancer invading the prostate or the urinary bladder are candidates for total pelvic exenteration. Pelvic exenteration for recurrent cervical and endometrial cancer previously treated with radiochemotherapy and selected cases of primary advanced vulva cancer For patients with gynecologic cancer, pelvic exenteration is sometimes the only available curative treatment. Particularly patients with recurrent cervical and endometrial cancer previously treated with chemoradiation are considered candidates for pelvic exenteration. Selected cases of primary advanced vulva cancer are also considered for more extensive pelvic surgery such as modified anterior or posterior pelvic exenteration. In Norway, pelvic exenteration for recurrent cervical cancer is centralized to the Department for Gynecologic Oncology at the Oslo University Hospital and annually, approximately 10-15 patients are treated with total pelvic exenteration. An ongoing project in our Institution evaluating the clinical outcome of 95 patients treated with open pelvic exenteration for one of the above mentioned diagnoses revealed that about 50 % of the patients developed at least one severe complication (grade 3 or above according to the contracted Accordion severity grading system of surgical complications). 87% had negative surgical margins on final histology, but after median follow up time of 3.2 years, 59% of the patients had relapsed. About a third of those were central/pelvic recurrences. The high complication rate warrants further improvement of the surgical technique and minimally invasive surgery has emerged as a promising approach for selected patients (16, 17). Recently, case reports utilizing laparoscopic robot-assisted surgery have been published (18, 19). The reports indicate satisfactory oncological results and less surgical morbidity compared to open surgery. In many of the case reports on gynecological exenterations the reconstruction of the urinary tract is done extra-corporally. In our Institution, robot-assisted intra-corporal urinary diversion is well established. Thus, the robotic approach for pelvic exenterations is attractive and feasible in our multidisciplinary surgical group. Study design Open label observational study. Study objectives This study is a feasibility study of laparoscopic robot-assisted total pelvic exenteration for pelvic cancers. Feasibility will be assessed through: Determining the R0 resection rate in included study patients Assessment of conversion rate to open surgery Assessment of perioperative and postoperative complications

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Locally Advanced Pelvic Cancer That Require Pelvic Exenteration
Keywords
robot-assisted, pelvic exenteration, minimally invasive surgery, locally advanced rectal and sigmoid cancers, localized central pelvic recurrence of cervical cancer or endometrial cancers, feasibility

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Open label observational study
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Locally advanced pelvic cancer that requires total pelvic exenteration
Arm Type
Experimental
Arm Description
Adult patients (>18 years) with locally advanced pelvic cancer that require pelvic exenteration considered eligible for robot- assisted minimally invasive surgery by the respective multidisciplinary teams
Intervention Type
Procedure
Intervention Name(s)
robot-assisted total pelvic exenteration
Intervention Description
Patients with locally advanced pelvic cancer that require pelvic exenteration considered eligble, are operated minimmally invasive robot-assisted
Primary Outcome Measure Information:
Title
Rate of R0 resection
Description
R0 resection in oncological surgery means resection with circumferential margin >1mm from the tumour. R0 resection is considered as an important predictor for outcome.
Time Frame
up to three months from surgery
Secondary Outcome Measure Information:
Title
Rate of conversion from laparoscopic robot-assisted to open surgery
Description
a quality indicator and feasibility measure for the procedure
Time Frame
peroperative
Title
Rate and type of postoperative complications
Description
Any complications within the first 90 days after surgery
Time Frame
90 days
Title
Hospital length of stay
Description
How long the patient stay in Hospital after surgery
Time Frame
up to 4 weeks
Title
Disease free survival
Description
If the patient have any recurrent disease
Time Frame
up to 5 years
Title
Overall survival
Description
If the patient is alive
Time Frame
up to 5 years
Title
Quality of Life measured with the validated EORTC Quality of Life Questionnaire C-30 measurement tool (QoL C-30)
Description
Quality of Life measured before and on specific controles postoperative
Time Frame
Preoperative, and at 3, 6, 12 and 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients (>18 years) locally advanced pelvic cancer that require pelvic exenteration eligible for robot- assisted minimally invasive surgery by the respective multidisciplinary teams, may be included in the study. Exclusion Criteria: Any reason why the patient in the investigator's opinion is not suited for inclusion.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ebbe B Thorgersen, MD PhD
Phone
+4748144121
Email
ebbtho@rr-research.no
First Name & Middle Initial & Last Name or Official Title & Degree
Arne M Solbakken, MD
Phone
+4748281082
Email
arne.mide.solbakken@icloud.com
Facility Information:
Facility Name
Oslo University Hospital The Radium Hospital
City
Oslo
Country
Norway
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ebbe B Thorgersen, MD PhD
Phone
48144121
Email
ebbtho@rr-research.no

12. IPD Sharing Statement

Learn more about this trial

Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers

We'll reach out to this number within 24 hrs