Locally Advanced Pelvic Cancer That Require Pelvic ExenterationNCT05186493
Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers
A study testing robot-assisted total pelvic exenteration in people with Locally Advanced Pelvic Cancer That Require Pelvic Exenteration, run by Oslo University Hospital at 1 site in Norway.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Locally Advanced Pelvic Cancer That Require Pelvic Exenteration
- What is being tested?
- robot-assisted total pelvic exenteration
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteNorway
- Study dates
- 1 Nov 2021to 1 Dec 2030
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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.
Who cannot join
- Any reason why the patient in the investigator's opinion is not suited for inclusion.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Norway1 site, 1 recruiting
- Recruiting
Oslo University Hospital The Radium Hospital
Oslo
Ebbe B Thorgersen, MD PhD, 48144121, ebbtho@rr-research.no
About this study
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
Read more
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.
Read the 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
- Being tested
- robot-assisted total 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
- Medical subject headings
- Endometrial Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
robot-assisted total pelvic exenterationProcedure or surgery
Patients with locally advanced pelvic cancer that require pelvic exenteration considered eligble, are operated minimmally invasive robot-assisted
| Study group | Role | What they receive |
|---|---|---|
| Locally advanced pelvic cancer that requires total pelvic exenteration | Experimental | 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 Receives: Procedure: robot-assisted total pelvic exenteration |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: up to three months from surgery
Secondary outcomes (6)
Rate of conversion from laparoscopic robot-assisted to open surgery
a quality indicator and feasibility measure for the procedure
Measured: peroperative
Rate and type of postoperative complications
Any complications within the first 90 days after surgery
Measured: 90 days
Hospital length of stay
How long the patient stay in Hospital after surgery
Measured: up to 4 weeks
Disease free survival
If the patient have any recurrent disease
Measured: up to 5 years
Overall survival
If the patient is alive
Measured: up to 5 years
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
Measured: Preoperative, and at 3, 6, 12 and 36 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jan 2022
- Study start1 Nov 2021
- Primary completion1 Dec 2025 (estimated)
- Study completion1 Dec 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Locally Advanced Pelvic Cancer That Require Pelvic ExenterationStudies of the same condition, open and under way.
- More trials run by Oslo University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Open label observational study
- Masking
- None (open label)
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Oslo University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ebbe Billmann Thorgersen, Oslo University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05186493
- Sponsor's protocol ID
- 286145
- Status last verified
- Apr 2024
- First submitted
- 26 Nov 2021
- Last updated
- 3 Apr 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Apr 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers
- ClinicalTrials.gov ID
- NCT05186493
- Acronym / sponsor ID
- 286145
- 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
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Oslo University HospitalUniversity, hospital or other
- Study start
- 1 Nov 2021 (actual)
- Primary completion
- 1 Dec 2025 (estimated)
- Study completion
- 1 Dec 2030 (estimated)
- First posted
- 11 Jan 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Open label observational study
| Arm | Type | Receives |
|---|---|---|
| Locally advanced pelvic cancer that requires total pelvic exenteration | Experimental | Procedure: robot-assisted total pelvic exenterationAdult 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 |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (1 listed)
- Any reason why the patient in the investigator's opinion is not suited for inclusion.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| robot-assisted total pelvic exenterationPatients with locally advanced pelvic cancer that require pelvic exenteration considered eligble, are operated minimmally invasive robot-assisted | Procedure or surgery | Locally advanced pelvic cancer that requires total pelvic exenteration |
Primary outcome
Rate of R0 resection
Time frame: up to three months from surgery
R0 resection in oncological surgery means resection with circumferential margin >1mm from the tumour. R0 resection is considered as an important predictor for outcome.
6 secondary outcomes
Rate of conversion from laparoscopic robot-assisted to open surgery
Time frame: peroperative
Rate and type of postoperative complications
Time frame: 90 days
Hospital length of stay
Time frame: up to 4 weeks
Disease free survival
Time frame: up to 5 years
Overall survival
Time frame: up to 5 years
Quality of Life measured with the validated EORTC Quality of Life Questionnaire C-30 measurement tool (QoL C-30)
Time frame: Preoperative, and at 3, 6, 12 and 36 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Apr 2024.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing robot-assisted total pelvic exenteration in people with Locally Advanced Pelvic Cancer That Require Pelvic Exenteration, run by Oslo University Hospital at 1 site in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 3 Apr 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ebbe B Thorgersen, MD PhD (+4748144121, ebbtho@rr-research.no), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Rate of R0 resection (time frame: up to three months from surgery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2024.