Prevention of Postoperative Complications by Negative Pressure Therapy After Complex Breast Cancer Surgery
- Conditions
- Breast Cancer
- Interventions
- Procedure: Negative pressure therapy (NPT)Procedure: Dressing
- Registration Number
- NCT06265558
- Lead Sponsor
- Institut du Cancer de Montpellier - Val d'Aurelle
- Brief Summary
There is little scientific data concerning the use of negative pressure therapy after immediate breast reconstruction.
That strategy of treatment-reconstruction has expanded increasingly since the last years.
The current literature reports only 3 studies on the use of preventive negative pressure therapy in oncologic breast surgery.
Moreover, all three are retrospective, case-control studies with serious limitations.
The largest published series reports a reduction in the overall complication rate from 15.9% to 8.5%, and a significant reduction in several criteria: infection, scar dehiscence and necrosis. However, the study presents significant biases, with non-comparable populations in terms of comorbidities, surgical procedure performed, inclusion periods (and therefore experience in performing oncological surgery).
There was also a high probability of under-assessment or postponement of post-operative complications, which is typical of published retrospective surgical studies.
The published results therefore strongly encourage further investigation of negative pressure therapy in oncological breast surgery.
- Detailed Description
In 2022, excisional surgery is still one of the mainstays of breast cancer treatment. The excisional surgery is often combined with adjuvant treatments, which may include medical treatments such as chemotherapy, targeted therapies and immunotherapy, hormone therapy and radiotherapy. All these treatments have toxicities that impact on patients' quality of life.
One of the main complications of surgery is scarring. The rate is around 2% for "simple" breast surgery (conservative breast surgery - total mastectomy). This rate can rise sharply in the case of "complex" breast surgery, such as high-level oncoplasty, or mastectomy with Immediate Breast Reconstruction (IBR). This rate of surgical wound complications (ischemia, necrosis, dehiscence, infection) reached 20% in our local series of Immediate Breast Reconstruction (IBR) by prosthesis. This rate may exceed 30% in some series, depending on the surgical technique and the population, in cases of smoking, diabetes, previous radiotherapy, obesity and large breast volume. The increasing prevalence of these risk factors in the population means that scarring disorders must be taken into account in daily cancer care.
The impact of these scarring disorders is manifold:
* Delayed initiation of adjuvant therapy with an impact on overall survival.
* Cosmetic impact of scarring
* Possible loss of prosthetic breast reconstruction
* Patient dissatisfaction, with increased burden of care
* Overall impact on patient quality of life
* Economic impact linked to the length of care over time (consumption of dressing materials and personal time) Preventing the onset of wound-healing disorders is therefore vital in order to avoid these multiple consequences for the patient and the healthcare system.
In breast surgery, the use of preventive NPT (Negative Pressure Therapy) has been little studied. The NPT has been used mainly in cosmetic surgery procedures such as breast reduction, with results in favor of NPT. The most comprehensive study is a multicenter randomized trial which included 200 patients scheduled for bilateral breast reduction. In this trial, the comparison was made between the 2 breasts, each patient being her own control. The calculation of the number of subjects was based on a reduction in the complication rate from 20% to 10% (i.e., a 50% reduction). The study was positive, showing a reduction in the dehiscence rate at day 21 from 26% to 16%. In this study, patients were under-selected, and around 40% had risk factors for complications. A second randomized study, with similar methodology and judgment criteria, included 32 patients undergoing bilateral breast reduction. The results of this study are significant, but unfortunately there weren't much detail in the publication.
There is little scientific data concerning the use of negative pressure therapy after immediate breast reconstruction. There are very few data on the use of Negative pressure Therapy (NPT) after immediate Breast Reconstruction (IBR), a treatment-reconstruction strategy that has been expanding rapidly since recent years. The current literature reports only 3 studies on the use of preventive Negative pressure Therapy (NPT) in oncologic breast surgery. All three are retrospective, case-control studies with serious limitations. The largest published series involved 356 patients and 665 breasts. A reduction was reported in the overall complication rate from 15.9% to 8.5%, and a significant reduction in several criteria: infection, seroma, scar dehiscence and necrosis. However, the study presents significant biases, with non-comparable populations in terms of co-morbidities, surgical procedure performed, inclusion periods (and therefore experience in performing oncological surgery). There was also a high probability of under-assessment or postponement of post-operative complications, which is typical of published retrospective surgical studies.
The published results therefore strongly encourage further investigation of Negative Pressure Therapy (NPT) in oncological breast surgery.
Our hypothesis, then, is that preventive NPT in the immediate post-operative phase of complex breast surgery can prevent the onset of post-operative scarring disorders and shorten the time to complete healing.
To date, there are no randomized prospective studies of NPT in complex oncologic breast surgery. Randomized studies already published in general surgery provide a good level of evidence for the efficacy of NPT in preventing local post-operative complications. The latest systematic review and meta-analysis found a reduction in the risk of surgical site infection, from 13% to 8.8%, all types of surgery included. The benefit on the risk of dehiscence in general surgery is less strong, but a 30% reduction was found in a meta-analysis of studies involving only a preventive NPT device, a device widely used throughout the world.
In view of these results from randomized trials in general surgery and non-oncological breast surgery, and the results of retrospective studies in oncological breast surgery, a randomized trial must be carried out. This randomized controlled trial will be pragmatic, incorporating an intermediate analysis, given the endpoint evaluating the reduction in complications in a surgical context, to rapidly meet our objectives with a sufficient level of evidence to have an immediate impact on patients and modify practice.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 254
-
Female ≥ 18 years
-
Patient with unilateral invasive or in situ breast carcinoma
-
Patient with or without neoadjuvant treatment
-
Patient presenting an indication for complex breast surgery by mastectomy with immediate breast reconstruction by implant or oncoplasty by T-shaped mammoplasty.
-
Patient presenting at least one of the following risk factors for scarring disorders:
- Obesity with Body Mass Index BMI ≥ 30 and/or Cup size ≥ E
- Active smoking or smoking cessation for less than one month
- Diabetes
- History of homolateral breast radiotherapy
- Long-term corticosteroid therapy
-
Patient to have signed informed consent prior to study entry
-
Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests and other study procedures.
-
Patient affiliated with a health insurance plan.
- Legal incapacity or limited legal capacity. Medical or psychological conditions preventing the patient from completing the study or signing the consent form.
- Pregnant or breast-feeding patient
- Patient under guardianship or safeguard of justice
- Patient participating in an interventional study with the objective of wound healing
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Negative pressure therapy (NPT) Negative pressure therapy (NPT) Immediate post-operative negative pressure therapy Standard care Dressing Conventional post-operative care
- Primary Outcome Measures
Name Time Method Rate of patients with post-operative scarring trouble From baseline to 30 days after surgery Number of patients with post-operative scarring trouble divided by the total number of patients operated on in the trial.
- Secondary Outcome Measures
Name Time Method Surgical complication rate by Clavien-Dindo classification Approximately 10 days, from surgery to hospital discharge The Clavien-Dindo classification of surgical classifications is used throughout surgery for grading adverse events (complications) which occur as a result of surgical procedures. It includes 5 grades from grade 1 (recourse to usual postoperative treatments) to Grade 5 (death).
Rate of patients with a surgical site infection From baseline to 90 days after the surgery Number of patients with surgical site infection divided by total number of patients operated on in the trial.
Rate of patients with at least one rehospitalization Frm baseline to 90 days after the surgery Number of patients with at least one rehospitalization divided by total number of patients operated on in the trial.
Surgical revision rate From baseline to 90 days after the surgery Number of patients with repeat surgery divided by the total number of patients operated on in the trial.
Time to initiation of adjuvant therapy Approximately 3 months, from surgery to beginning of adjuvant therapy Number of days between surgery and initiation of adjuvant therapy
Patient satisfaction about cosmetic result evaluated using the BR23 questionnaire From baseline to 15 days then to 30 and 90 days after surgery The QLQ-BR23 incorporates five multi-item scales to assess body image, sexual functioning, systemic therapy side effects, breast symptoms, and arm symptoms.
Medical cost of post-surgery care From baseline to 90 days after surgery There will be a comparison between two arms. The medical cost of post-surgery care will be calculated on the basis of data such as number and type of dressings, consumables, time spent by the nurse, reason for hospital consultations and hospitalization, type of transport with home-hospital distance.
Quality of life evaluated by questionnaire QLQ-C30 (Version 3) From baseline to 15 days then to 30 and 90 days after surgery The EORTC QLG Core Questionnaire (EORTC QLQ-C30) is a 30-item instrument designed to measure quality of life in all cancer patients.Version 3, incorporates five functional scales on physical (PF), role (RF), cognitive (CF), emotional (EF) and social (SF) functioning, three symptom scales on fatigue (FA), pain (PA) and nausea and vomiting (NV), single items assessing dyspnoea (DY), insomnia (SL), loss of appetite (AP), constipation (CO) and diarrhoea (DI), one item assessing perceived financial impact (FI) and a global health status/QoL scale (Global QoL). Each item is scored in one of four categories 1) 'Not at all', 2) 'A little', 3) 'Quite a bit' 4) 'Very much', with the exception of 'Global QoL'which ranges from 1) 'Very poor' to 7) 'Excellent'.
Scoring of the items in the PF scale in the latest revision of EORTC QLQ-C30, Version 3 is extended to the four-point scale instead of the previous 'Yes/No' dichotomyQuality of life evaluated by questionnaire QLQ-BReast cancer (BR23) From baseline to 15 days then to 30 and 90 days after surgery The Breast Cancer module is a supplementary questionnaire module to be employed in conjunction with the QLQ-C30. The QLQ-BR23 incorporates five multi-item scales to assess body image, sexual functioning, systemic therapy side effects, breast symptoms, and arm symptoms. All of the scales and single-item measures range in score from 0 to 100. A high score for the functional scales represents a high/healthy level of functioning, whilst a high score for the symptom scales represents a high level of symptomatology or problems.
Trial Locations
- Locations (7)
Centre Georges-François Leclerc
🇫🇷Dijon, Côte d'Or, France
Centre Hospitalier de Nîmes
🇫🇷Nîmes, Gard, France
Institut Bergonié
🇫🇷Bordeaux, Gironde, France
Centre Hospitalier de Montpellier
🇫🇷Montpellier, Hérault, France
Institut régional du Cancer de Montpellier
🇫🇷Montpellier, Hérault, France
Institut de Cancérologie de l'Ouest
🇫🇷Angers, Maine Et Loire, France
Centre Léon Bérard
🇫🇷Lyon, Rhône, France