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NCT07408999Not yet recruiting

Totally Versus Hybrid Minimally Invasive Esophagectomy for Esophageal Cancer

Totally Versus Hybrid Minimally Invasive Esophagectomy for Esophageal Cancer - A Multicentric Phase III Prospective Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 13 Feb 2026

Brief summary (registry, in English)

Esophageal and gastroesophageal junction cancers remain associated with poor survival despite progress in multimodal treatment. Surgery, especially Ivor-Lewis esophagectomy, combined with peri-operative therapy improves survival but is burdened by major morbidity, mainly respiratory and anastomotic complications, which compromise recovery and adjuvant treatment. Minimally invasive approaches such as totally minimally invasive esophagectomy (TMIE) have shown potential to reduce postoperative morbidity compared to the hybrid approach (HE). However, existing studies are heterogeneous, mostly retrospective, and insufficient to establish a standard. This trial aims to provide high-level evidence comparing TMIE to HE, including robotic techniques, with integrated analyses of clinical outcomes, quality of life, and health economics.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
327 (estimated)
First submitted
23 Jan 2026
Start date
31 Mar 2026
Primary completion date
30 Jun 2028
Lead sponsor
University Hospital, Lille
NCT number
NCT07408999

What you commit to

  • Study type: Interventional
  • Planned participants: 327
  • From 31 Mar 2026 to the primary completion date, 30 Jun 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Non inclusion criteria for screening - part A (for patients receiving a neo-adjuvant treatment)
  • Patients with prior thoracic surgery or thoracic traum of the right hemithorax
  • Pregnant or breastfeeding woman or patient expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 6 months after the last dose of adjuvant chemotherapy
  • Distant metastatic extension
    • Non inclusion criteria before surgery (after neo-adjuvant treatment or for patients receiving primary surgery)
  • Patients with prior thoracic surgery or thoracic traum of the right hemithorax
  • Pregnant or breastfeeding woman or patient expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 6 months after the last dose of adjuvant chemotherapy

Other illness

  • Documented liver cirrhosis or portal hypertension
  • Recent myocardial infarction (less than 6 months old) or progressive coronary artery disease
  • Synchronous cancer, other than subcarinal esophageal
  • Neoplasic history except for cancers without recurrence after at least 5 years of surveillance
  • History of xyphopubic laparotomy
  • ASA score\> 3
    • Disease-related non-inclusion criteria
  • Documented liver cirrhosis or portal hypertension
  • Recent myocardial infarction (less than 6 months old) or progressive coronary artery disease
  • Synchronous cancer, other than subcarinal esophageal
  • Neoplasic history except for cancers without recurrence after at least 5 years of surveillance
  • History of xyphopubic laparotomy
  • IESG ≤ -5 (Very high risk patients)
    • Disease-related non-inclusion criteria

Other

  • Patient-related non-inclusion criteria
  • Performance status 3 or 4
  • Distal arteritis from stage IIb (200 m) of Leriche and Fontaine
  • Patient refusal
  • Patient under guardianship or curatorship
  • Histology other than squamous cell carcinoma or adenocarcinoma
  • Tumors of the upper third of the thoracic esophagus, cervical esophagus or pharyngo-esophageal junction or tumor of the esogastric junction Siewert 3
  • Supraclavicular nodes invaded clinically or on puncture
  • Recurrent nerve paralysis
  • Evidence of extension to the tracheobronchial tree
  • Signs of mediastinal invasion (vertebral adhesion, aortic overlap \> 90°, invasion of unresectable neighboring organs such as the aorta, trachea…)
  • Performance status 3 or 4
  • Forced expiratory volume in 1 second \< 1000 ml
  • Distal arteritis from stage IIb (200 m) of Leriche and Fontaine
  • Weight loss of more than 15% of body weight, not recovered after appropriate nutritional management
  • Patient refusal
  • Patient under guardianship or curatorship
  • ASA score\> 3
  • Histology other than squamous cell carcinoma or adenocarcinoma
  • Tumors of the upper third of the thoracic esophagus, cervical esophagus or pharyngo-esophageal junction or tumor of the esogastric junction Siewert 3
  • Supraclavicular nodes invaded clinically or on puncture
  • Recurrent nerve paralysis
  • Evidence of extension to the tracheobronchial tree
  • Signs of mediastinal invasion (vertebral adhesion, aortic overlap \> 90°, invasion of unresectable neighboring organs such as the aorta, trachea…)
  • Distant metastatic extension

Who the study is looking for

  • Age ≥ 18 years and ≤ 80 years For patients between 70 and 80 years old : score G8 ≥ 14 or oncogeratrician approval
  • Squamous cell carcinoma or adenocarcinoma of the esophagus or esogastric junction
  • Clinical stage T1, T2, T3, T4a, N0-N3, M0 before any treatment
  • Tumors of the middle or lower third of the esophagus, or tumor of the esogastric junction Siewert 1 or 2
  • With or without neoadjuvant (radio) chemotherapy ± targeted therapy
  • Disease deemed curatively resectable preoperatively
  • Requiring a 2-stage Ivor-Lewis esophagectomy
  • Performance status 0, 1 or 2
  • Patient capable of receiving either surgical treatment
  • Patient informed of the terms of the study and having given written consent
  • Patient able to read and understand the language and content of the study documents and agreeing to adhere to the protocol requirements.
  • Covered by a medical/health insurance
  • Willingness and ability to comply with scheduled visits and study procedures
  • Age ≥ 18 years and ≤ 80 years For patients between 70 and 80 years old : score G8 ≥ 14 or oncogeratrician approval
  • Squamous cell carcinoma or adenocarcinoma of the esophagus or esogastric junction
  • Clinical stage T1, T2, T3, N0-N3, M0 before surgery
  • Tumors of the middle or lower third of the esophagus, or tumor of the esogastric junction Siewert 1 or 2
  • With or without neoadjuvant (radio) chemotherapy ± targeted therapy
  • Disease deemed curatively resectable preoperatively
  • Requiring a 2-stage Ivor-Lewis esophagectomy
  • Performance status 0, 1 or 2
  • Patient capable of receiving either surgical treatment
  • Patient informed of the terms of the study and having given written consent
  • Patient able to read and understand the language and content of the study documents and agreeing to adhere to the protocol requirements.
  • Covered by a medical/health insurance
  • Willingness and ability to comply with scheduled visits and study procedures

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.