Robotic Low Rectum Anterior Resection
- Conditions
- Rectum Cancer
- Interventions
- Other: Clinical database
- Registration Number
- NCT04015804
- Lead Sponsor
- Institut du Cancer de Montpellier - Val d'Aurelle
- Brief Summary
The laparoscopic approach for total mesorectal excision (L-TME) results improved short-term outcomes. However this approach has technical limitations when the pelvis is narrow and deep. Indeed there is a limited mobility of straight laparoscopic instruments and associated loss of dexterity, unstable camera view and compromised ergonomics for the surgeon. Robotic technology was developed to reduce these limitations and offers the advantages of intuitive manipulation of laparoscopic instruments with wrist articulation, a 3-dimensional field of view, a stable camera platform with zoom magnification, dexterity enhancement and an ergonomic operating environment. A major advantage of the robotic approach is the surgeon's simultaneous control of the camera and of the two or three additional instruments. This advantage facilitates traction and counter-traction. The technological advantages of robotic surgery should also allow a finer dissection in a narrow pelvic cavity.
- Detailed Description
The laparoscopic approach for laparoscopic total mesorectal excision (L-TME) results improved short-term outcomes and provides a clearer intraoperative view compared with the open approach in a deep and narrow pelvis. Preliminary results from the COLOR II trial confirmed improved patient recovery and similar safety, same resection margins and completeness of resection using L-TME compared with the results achieved with open surgery.Results from the CLASICC trial supported the use of laparoscopic surgery for colorectal cancer and showed no difference between laparoscopically-assisted TME and conventional open resection at 10 years post-procedure in terms of overall survival, disease-free survival and local recurrence.
Despite these positive clinical outcomes for L-TME, laparoscopic resection of rectal cancer, especially in a deep and narrow pelvis, is technically demanding and demands a long learning curve. Technical limitations include limited mobility of straight laparoscopic instruments and associated loss of dexterity, unstable camera view and compromised ergonomics for the surgeon. These limitations could explain the conversion rate which remained at 17% in the last COLOR II trial.2 In order to avoid this drawback, we have described for patients with high-risk of conversion, the trans-anal endoscopic proctectomy (TAEP) approach performed with the Transanal Endoscopic Operation (TEO) device.This trans-anal procedure is also called trans anal minimally invasive surgery (TAMIS) if a laparoscopic port is used.
Robotic technology was developed to reduce these limitations and offers the advantages of intuitive manipulation of laparoscopic instruments with wrist articulation, a 3-dimensional field of view, a stable camera platform with zoom magnification, dexterity enhancement and an ergonomic operating environment. A major advantage of the robotic approach is the surgeon's simultaneous control of the camera and of the two or three additional instruments. This advantage facilitates traction and counter-traction. The technological advantages of robotic surgery should also allow a finer dissection in a narrow pelvic cavity. However, total robotic surgery for rectal cancer is still technically challenging and involves two operative fields (splenic flexure and rectum), potential collision of the robotic arms and lack of tactile feedback.
Reports of robotic and laparoscopic rectal cancer surgery outcomes showed similar intraoperative results and morbidity, postoperative recovery and short-term oncologic outcomes.However, longer operation times have been described as a disadvantage of the robotic system, compared with conventional laparoscopy. On the other hand, all meta-analyses comparing robotic total mesorectal excision (R-TME) and L-TME concluded in reduction of the conversion rate.
Since 2007, the rectal surgery with robotic assistance is booming. To date, seven meta-analyzes have been published. All show that the robot exceeds laparoscopy to reduce the conversion rate. The last two meta-analyzes that had gathered more than 800 patients undergoing robotic surgery have again highlighted the contribution of the robot to secure the radial margin and decrease sexual sequelae. However, there is not so far from Phase 3 randomized trial dealing with the subject. The ROLARR protocol was completed in late 2014 (Ph III laparoscopy / Robot), the first results are published in late 2015.
The interest of a European multicenter ambispective (retrospective and prospective) database is fundamental because this early work suggests that the robot can make more for specific subgroups of patients, particularly in high surgical risk patients (Male, narrow pelvis, high BMI, mesorectal fat, large tumor of the anterior and middle third).
The largest series of R-TME stems from the US national cancer database (965 patients operated by R-TME) and confirms a 9.5% conversion rate compared to 16.4% with L-TME (p \< 0.001).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 833
- Men or women ≥ 18 years
- Introducing rectal cancer, colorectal junction eligible to robotic surgery support from June 2015
- Treatment Naive for this cancer
- Enjoying a social protection scheme (For France only)
- Patient followed in the participant center
- Male or female age (s) under 18 years
- Private person of liberty or under supervision (including guardianship)
- People who do not speak French (For France only)
- Major Nobody unable to consent
- Patient GROG-R01 already included in the base
- Patient Refusal
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Clinical database Clinical database -
- Primary Outcome Measures
Name Time Method Conversion rate for robotic surgery 5 years
- Secondary Outcome Measures
Name Time Method Number of robot docking 5 years Post-operative morbidity 5 years Anatomo-pathological curability criteria 5 years Median of hospitalization time 5 years Operating time 5 years
Trial Locations
- Locations (19)
Hôpital Européen
🇫🇷Marseille, Bouches Du Rhône, France
Institut Paoli Calmettes
🇫🇷Marseille, Bouches Du Rhône, France
Clinique Saint Jean du Languedoc
🇫🇷Toulouse, Haute Garonne, France
Centre François Baclesse
🇫🇷Caen, Calvados, France
CHU Dupuytren
🇫🇷Limoges, Haute Vienne, France
Hôpital privé d'Anthony
🇫🇷Antony, Hauts De Seine, France
Institut régional du cancer de Montpellier
🇫🇷Montpellier, Hérault, France
Hôpital Michalon
🇫🇷Grenoble, Isère, France
CHU de Nantes
🇫🇷Nantes, Loire Atlantique, France
CHR Orléans
🇫🇷Orléans, Loiret, France
Institut de Cancérologie de l'Ouest
🇫🇷Saint-Herblain, Loire Atlantique, France
CHU de Nancy
🇫🇷Vandœuvre-lès-Nancy, Lorraine, France
Centre Oscart Lambret
🇫🇷Lille, Nord, France
Institut Gustave Roussy
🇫🇷Villejuif, Val De Marne, France
Hôpital européen Georges Pompidou
🇫🇷Paris, France
Hôpital Diaconesses
🇫🇷Paris, France
Centre Hospitalier-Princesse Grace
🇲🇨Monaco, Monaco
UCL
🇧🇪Bruxelles, Belgium
Clinique Kennedy
🇫🇷Nîmes, Gard, France