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Cost-utility of Two Strategies of Perineal Reconstruction After Abdominoperineal Resection for Anorectal Carcinoma (GRECCAR-9)

Primary Purpose

Abdominoperineal Resection

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Biological mesh
Primary perineal wound closure
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Abdominoperineal Resection focused on measuring anorectal carcinoma, perineal filling, cost-utility analysis, biological meshes, primary perineal wound closure

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 18
  • Eastern Cooperative Oncology Group performance status score of 2 or less
  • Histologically proven rectal adenocarcinoma or anal canal epidermoïd carcinoma
  • Abdominoperineal resection indication after multidisciplinary team discussion:

    • for rectal adenocarcinoma: circumferential MRI margin equal or less than 1 mm from closest tumoral structure and a striated muscular layer (levator ani or external anal sphincter)
    • for epidermoid carcinoma: residual or recurrent tumour after chemoradiotherapy.
  • Voluntary written informed consent
  • Patients with social security insurance or equivalent social protection

Exclusion Criteria:

  • T4 tumour needing a surgical extensive resection with reconstruction by a musculocutaneous flap
  • Metastasis disease deemed unresectable with curative intent
  • Previous pelvic radiotherapy for another disease than the rectal or anal cancer
  • Immunosuppressive drugs treatment
  • Uncontrolled diabetes (glycosylated hemoglobin (HbA1c) > 8 % despite adequate therapy)
  • Patient under juridical protection.
  • Sensitivity to porcine derived products.
  • Enrolment in trial with overlapping primary endpoint.
  • Pregnant women
  • Breastfeeding women

Sites / Locations

  • Amiens University Hospital
  • Angers University Hospital
  • Besançon University Hospital
  • Bordeaux University Hospital
  • Caen University Hospital
  • Clermont-Ferrand University Hospital
  • Grenoble University Hospital
  • Centre Oscar LambretRecruiting
  • CHRU Lille
  • Lyon University Hospital
  • Paoli Calmettes Institut
  • Institut de Cancérologie de Lorraine
  • Nancy University Hospital
  • Nantes University Hospital
  • Saint-Antoine Hospital
  • Rouen University Hospital
  • University Hospital of ToulouseRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm with biological mesh

Arm with primary perineal wound closure

Arm Description

The intervention consists of perinal reconstruction using biological mesh (Cellis prosthesis from Meccellis Biotech, reference C1015E size 10x15cm)

The intervention consists of perinal reconstruction by primary perineal wound closure

Outcomes

Primary Outcome Measures

Incremental Cost-Utility Ratio (ICUR)
The primary endpoint in this study is based on the assessment of the incremental cost-utility ratio at 1 year, from the collective perspective between biological mesh perineal reconstructions versus. primary perineal closure in patients operated for anorectal carcinoma with proven rectal adenocarcinoma or anal canal epidermoid carcinoma.

Secondary Outcome Measures

Perineal wound healing
The perineal wound healing will be assessed using the Southampton wound assessment scale (6-point scale ranging from 0=normal healing to V=deep or severe wound infection)
Pain intensity
assessed on an 11-point Numeric Rating Scale (NRS) at baseline before surgical procedure and at least 3 times a day during hospital stay. Thereafter, patients will rate their pain intensity in a patient subject diary every day and immediately before each use of pain medication
Health related Quality of life
Health related quality of life will be assessed using the EuroQOL EQ-5D-5L questionnaire
Perineal complications
Perineal complications include: Perineal wound infection defined as a swelling of the wound or surrounding tissues with purulent discharge Breakdown of the perineal wound included any wound dehiscence, sinus or ulcer Pelvic abscess included a fluid collection in the pelvis Perineal evisceration defined by exposure of the pelvic cavity through the perineal wound Perineal hernia symptomatic or not Perineal sinus defined as an incomplete healing after 6 months

Full Information

First Posted
July 12, 2016
Last Updated
March 2, 2021
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT02841293
Brief Title
Cost-utility of Two Strategies of Perineal Reconstruction After Abdominoperineal Resection for Anorectal Carcinoma
Acronym
GRECCAR-9
Official Title
Cost-utility Evaluation of Two Strategies of Perineal Reconstruction After Abdominoperineal Resection for Anorectal Carcinoma: Perineal Filling With Biological Meshes vs. Primary Perineal Wound Closure
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Recruiting
Study Start Date
February 7, 2021 (Actual)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
February 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

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
Abdominoperineal resection performed for anorectal tumors leaves a large pelvic and perineal defect causing a high rate of morbidity of the perineal wound (40 - 60 %). Biological meshes offer possibility for a new standard of perineal wound reconstruction. Perineal filling with biological mesh is expected to increase quality of life by reducing perineal morbidity.
Detailed Description
Perineal wound problems after abdominoperineal resection (APR) in the context of cancer are frequent. These types of resection problems occur because of wound complications caused by large perineal defects. Indeed, perineal wound complications, perineal abscess, wound dehiscences, chronic fistulas and sinuses lengthen the hospital stays. Futhermore, the standardization of the surgery since the late 2000s and the extralevator technique lead a larger defect and increase i perineal complications. Several strategies are used to decrease the complication rate. Closure by direct approximation of the pelvic muscles leads to a rate of major complication up to 57% depending on the series. Musculocutaneous flaps help to reduce this rate (16- 65%) but they generate their own morbidity, require experience and increase the costs of care. Finally, the use of biologic meshes since the beginning of 2010 seems to have improve the healing process. However, results are still variable and the only randomized study comparing direct closure and mesh closure showed no significant results at one year. Another ongoing randomized trial is comparing gluteus maximus flap to mesh closure and focusing on physical performances. This increase in post-operative complications and their consequences causes an increase in costs. In addition, they affect the patients' quality of life and lead to a loss of productivity. From an oncological point of view, perineal scarring problems can cause a delay in the adjuvant therapeutic sequence. Few studies have highlighted the efficiency of perineal wound complications, using cost-effectiveness analyses. In order to clarify the best strategy comparing primary and mesh closure in term of cost effectiveness on perineal healing after ELAPE, we designed this randomized controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominoperineal Resection
Keywords
anorectal carcinoma, perineal filling, cost-utility analysis, biological meshes, primary perineal wound closure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm with biological mesh
Arm Type
Experimental
Arm Description
The intervention consists of perinal reconstruction using biological mesh (Cellis prosthesis from Meccellis Biotech, reference C1015E size 10x15cm)
Arm Title
Arm with primary perineal wound closure
Arm Type
Active Comparator
Arm Description
The intervention consists of perinal reconstruction by primary perineal wound closure
Intervention Type
Procedure
Intervention Name(s)
Biological mesh
Intervention Description
The intervention consists of suturing a biological mesh in the pelvic floor defect. The mesh will be sutured at each side of the coccyx or distal sacrum and directly to the residual pelvic floor muscle and fascia by using interrupted or continuous hand-sewn sutures with an appropriate amount of tension. The mesh that will be used is the Cellis prosthesis from Meccellis Biotech, reference C1015E which size is 10x15cm.
Intervention Type
Procedure
Intervention Name(s)
Primary perineal wound closure
Intervention Description
The intervention consists of stitching the ischioanal and subcutaneous fat using interrupted Vicryl sutures in one or two layers similar to primary perineal closure
Primary Outcome Measure Information:
Title
Incremental Cost-Utility Ratio (ICUR)
Description
The primary endpoint in this study is based on the assessment of the incremental cost-utility ratio at 1 year, from the collective perspective between biological mesh perineal reconstructions versus. primary perineal closure in patients operated for anorectal carcinoma with proven rectal adenocarcinoma or anal canal epidermoid carcinoma.
Time Frame
At 12 months
Secondary Outcome Measure Information:
Title
Perineal wound healing
Description
The perineal wound healing will be assessed using the Southampton wound assessment scale (6-point scale ranging from 0=normal healing to V=deep or severe wound infection)
Time Frame
At 1, 3, 6, 9 and 12 months
Title
Pain intensity
Description
assessed on an 11-point Numeric Rating Scale (NRS) at baseline before surgical procedure and at least 3 times a day during hospital stay. Thereafter, patients will rate their pain intensity in a patient subject diary every day and immediately before each use of pain medication
Time Frame
From date of randomization until the date of study participation end of patient, assessed up to 12 months
Title
Health related Quality of life
Description
Health related quality of life will be assessed using the EuroQOL EQ-5D-5L questionnaire
Time Frame
1 month, 3 months, 6 months, 9 months, 12 months
Title
Perineal complications
Description
Perineal complications include: Perineal wound infection defined as a swelling of the wound or surrounding tissues with purulent discharge Breakdown of the perineal wound included any wound dehiscence, sinus or ulcer Pelvic abscess included a fluid collection in the pelvis Perineal evisceration defined by exposure of the pelvic cavity through the perineal wound Perineal hernia symptomatic or not Perineal sinus defined as an incomplete healing after 6 months
Time Frame
Daily during hospitalization and at 1, 3, 6, 9 and 12 months after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 Eastern Cooperative Oncology Group performance status score of 2 or less Histologically proven rectal adenocarcinoma or anal canal epidermoïd carcinoma Abdominoperineal resection indication after multidisciplinary team discussion: for rectal adenocarcinoma: circumferential MRI margin equal or less than 1 mm from closest tumoral structure and a striated muscular layer (levator ani or external anal sphincter) for epidermoid carcinoma: residual or recurrent tumour after chemoradiotherapy. Voluntary written informed consent Patients with social security insurance or equivalent social protection Exclusion Criteria: T4 tumour needing a surgical extensive resection with reconstruction by a musculocutaneous flap Metastasis disease deemed unresectable with curative intent Previous pelvic radiotherapy for another disease than the rectal or anal cancer Immunosuppressive drugs treatment Uncontrolled diabetes (glycosylated hemoglobin (HbA1c) > 8 % despite adequate therapy) Patient under juridical protection. Sensitivity to porcine derived products. Enrolment in trial with overlapping primary endpoint. Pregnant women Breastfeeding women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Etienne BUSCAIL, MD
Phone
33-561322373
Email
buscail.e@chu-toulouse.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Cindy CANIVET, CRA
Email
canivet.c@chu-toulouse.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Etienne BUSCAIL, MD
Organizational Affiliation
University Hospital of Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Amiens University Hospital
City
Amiens
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Marc REGIMBEAU
Email
regimbeau.jean-marc@chu-amiens.fr
First Name & Middle Initial & Last Name & Degree
Jean-Marc REGIMBEAU
Facility Name
Angers University Hospital
City
Angers
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aurélien VENARA
First Name & Middle Initial & Last Name & Degree
Aurélien VENARA
Facility Name
Besançon University Hospital
City
Besançon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zaher LAKKIS
Email
zlakkis@chu-besancon.fr
First Name & Middle Initial & Last Name & Degree
Zaher LAKKIS
Facility Name
Bordeaux University Hospital
City
Bordeaux
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric Rullier
Email
eric.rullier@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Eric Rullier
Facility Name
Caen University Hospital
City
Caen
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arnaud ALVES
Email
alves-a@chu-caen.fr
First Name & Middle Initial & Last Name & Degree
Arnaud ALVES
Facility Name
Clermont-Ferrand University Hospital
City
Clermont-Ferrand
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne DUBOIS
Email
A_dubois@chu-clermontferrand.fr
First Name & Middle Initial & Last Name & Degree
Anne DUBOIS
Facility Name
Grenoble University Hospital
City
Grenoble
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bertrand TRILLING
Email
BTrilling@chu-grenoble.fr
First Name & Middle Initial & Last Name & Degree
Bertrand TRILLING
Facility Name
Centre Oscar Lambret
City
Lille
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mehrdad JAFARI
Email
m-jafari@o-lambret.fr
First Name & Middle Initial & Last Name & Degree
Mehrdad JAFARI
Facility Name
CHRU Lille
City
Lille
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume PIESSEN, MD
Email
Guillaume.piessen@chru.lille.fr
First Name & Middle Initial & Last Name & Degree
Guillaume PIESSEN
Facility Name
Lyon University Hospital
City
Lyon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eddy Cotte
Email
eddy.cotte@chu-lyon.fr
First Name & Middle Initial & Last Name & Degree
Eddy Cotte
Facility Name
Paoli Calmettes Institut
City
Marseille
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cécile De Chaisemartin
Email
dechaisemartin@ipc.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Cécile De Chaisemartin
Facility Name
Institut de Cancérologie de Lorraine
City
Nancy
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cécilia CERIBELLI
Email
c.ceribelli@nancy.unicancer.fr
First Name & Middle Initial & Last Name & Degree
Cécilia CERIBELLI
Facility Name
Nancy University Hospital
City
Nancy
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adeline GERMAIN
Email
a.germain@chru-nancy.fr
First Name & Middle Initial & Last Name & Degree
Adeline GERMAIN
Facility Name
Nantes University Hospital
City
Nantes
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emilie DUCHALAIS, MD
First Name & Middle Initial & Last Name & Degree
Emilie DUCHALAIS
Facility Name
Saint-Antoine Hospital
City
Paris
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérémie LEFEVRE
Email
jeremie.lefevre@aphp.fr
First Name & Middle Initial & Last Name & Degree
Jérémie LEFEVRE
Facility Name
Rouen University Hospital
City
Rouen
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Jacques Tuech
Email
jean-jacques.tuech@chu-rouen.fr
First Name & Middle Initial & Last Name & Degree
Jean-Jacques Tuech
Facility Name
University Hospital of Toulouse
City
Toulouse
ZIP/Postal Code
31059
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Etienne Buscail, MD
Email
buscail.e@chu-toulouse.fr
First Name & Middle Initial & Last Name & Degree
Cindy Canivet, CRA
Email
canivet.c@chu-toulouse.fr
First Name & Middle Initial & Last Name & Degree
Etienne Buscail, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33795299
Citation
Buscail E, Canivet C, Ghouti L, Kirzin S, Carrere N, Molinier L, Rosillo A, Lauwers-Cances V, Costa N; French Research Group of Rectal Cancer Surgery (GRECCAR Group). Randomised clinical trial for the cost-utility evaluation of two strategies of perineal reconstruction after abdominoperineal resection in the context of anorectal carcinoma: biological mesh repair versus primary perineal wound closure, study protocol for the GRECCAR 9 Study. BMJ Open. 2021 Apr 1;11(4):e043333. doi: 10.1136/bmjopen-2020-043333.
Results Reference
derived

Learn more about this trial

Cost-utility of Two Strategies of Perineal Reconstruction After Abdominoperineal Resection for Anorectal Carcinoma

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