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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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
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.

Ebbe B Thorgersen, MD PhD contact

+4748144121

ebbtho@rr-research.no

Arne M Solbakken, MD contact

+4748281082

arne.mide.solbakken@icloud.com

Norway1 site, 1 recruiting
  • Oslo University Hospital The Radium Hospital

    Oslo

    Ebbe B Thorgersen, MD PhD, 48144121, ebbtho@rr-research.no

    Recruiting

Other trials in Norway

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:

  1. Determining the R0 resection rate in included study patients
  2. Assessment of conversion rate to open surgery
  3. 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 groups in NCT05186493
Study groupRoleWhat they receive
Locally advanced pelvic cancer that requires total pelvic exenterationExperimentalAdult 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.

  1. 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)
  1. Rate of conversion from laparoscopic robot-assisted to open surgery

    a quality indicator and feasibility measure for the procedure

    Measured: peroperative

  2. Rate and type of postoperative complications

    Any complications within the first 90 days after surgery

    Measured: 90 days

  3. Hospital length of stay

    How long the patient stay in Hospital after surgery

    Measured: up to 4 weeks

  4. Disease free survival

    If the patient have any recurrent disease

    Measured: up to 5 years

  5. Overall survival

    If the patient is alive

    Measured: up to 5 years

  6. 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.

  1. First posted11 Jan 2022
  2. Study start1 Nov 2021
  3. Primary completion1 Dec 2025 (estimated)
  4. Study completion1 Dec 2030 (estimated)

Resources

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)
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

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.

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