Skip to content

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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02841293
Acronym
GRECCAR-9
Enrollment
140
Registered
2016-07-22
Start date
2021-02-07
Completion date
2024-02-29
Last updated
2021-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominoperineal Resection

Keywords

anorectal carcinoma, perineal filling, cost-utility analysis, biological meshes, primary perineal wound closure

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.

Interventions

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.

PROCEDUREPrimary perineal wound closure

The intervention consists of stitching the ischioanal and subcutaneous fat using interrupted Vicryl sutures in one or two layers similar to primary perineal closure

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Incremental Cost-Utility Ratio (ICUR)At 12 monthsThe 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

MeasureTime frameDescription
Perineal wound healingAt 1, 3, 6, 9 and 12 monthsThe 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 intensityFrom date of randomization until the date of study participation end of patient, assessed up to 12 monthsassessed 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 life1 month, 3 months, 6 months, 9 months, 12 monthsHealth related quality of life will be assessed using the EuroQOL EQ-5D-5L questionnaire
Perineal complicationsDaily during hospitalization and at 1, 3, 6, 9 and 12 months after surgeryPerineal 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

Countries

France

Contacts

Primary ContactEtienne BUSCAIL, MD
buscail.e@chu-toulouse.fr33-561322373
Backup ContactCindy CANIVET, CRA
canivet.c@chu-toulouse.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026