Fluorescence Image Guided Foregut Surgery (FOREGUT)
Primary Purpose
Esophageal Cancer, Gastric Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Near Infra-Red Fluorescence Guided Surgery
Sponsored by
About this trial
This is an interventional other trial for Esophageal Cancer focused on measuring Esophageal cancer, Gastric cancer, Lymphadenectomy, Complications, Anastomosis
Eligibility Criteria
Inclusion Criteria:
- Man or woman over 18 years old.
- Patient with resectable primitive esophageal or gastric cancer confirmed by biopsy without distant metastases
- Patient with no contraindications to anaesthesia and performance of esophageal and/or gastric surgery
- Patient able to receive and understand information related to the study and give written informed consent.
- Patient affiliated to the French social security system.
Exclusion Criteria:
- Patient undergoing emergency surgery (hemorrhage, occlusion or perforation).
- Presence of distant metastasis
- Patient at risk of allergy to indocyanine green or to other fluorescent compounds
- Pregnant or lactating patient.
- Patient in exclusion period (determined by a previous or a current study).
- Patient under the protection of justice.
- Patient under guardianship or trusteeship.
- Patient deprived of liberty
Sites / Locations
- Service de Chirurgie Digestive et Endocrinienne, NHCRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
NIR Fluorescence guided lymphadenectomy and anastomosis
Arm Description
Outcomes
Primary Outcome Measures
Evaluation of the usefulness of ICG fluorescence to guide lymphadenectomy in oncological esogastric resections
Additional detection (YES-NO) of lymph nodes after activation of the NIR fluorescence guidance system during lymphadenectomy.
Secondary Outcome Measures
Evaluation of the impact of fluorescence guidance on the number of resected lymph nodes in oncological esogastric resections
Number of lymph nodes, counted in anatomopathological analysis, obtained after fluorescence-guided lymphadenectomy in the esogastric oncology resections compared to historical data
Evaluation of the impact of fluorescence guidance in intraoperative evaluation of pre-anastomotic tissue perfusion
Anastomotic fistula rate after fluorescence control of pre-anastomotic vascularisation in oncological esogastric resections compared to historical data
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04734821
Brief Title
Fluorescence Image Guided Foregut Surgery
Acronym
FOREGUT
Official Title
Prospective Study on the Contribution of Fluorescence in the Guidance of Lymphadenectomy and in Peroperative Evaluation of Pre-anastomotic Tissue Perfusion in Laparoscopic Esogastric Oncologic Resections
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
February 1, 2024 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IHU Strasbourg
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
A high number of resected lymph nodes is an independent prognostic factor for improved survival after esophagectomy or gastrectomy for cancer. The quality of the lymphadenectomy is operator-dependent, as is the evaluation of the vascularization of the digestive structures that are anastomosed to restore digestive continuity after esophago-gastric resection. The aim of the study is to evaluate the impact of Indocyanine Green (ICG) and near infra-red (NIR) fluorescence imaging guidance in terms of number of lymph nodes resected and quality of gastrointestinal tract anastomoses in esophagogastric cancer surgery.
Detailed Description
In cancer surgery, an oncological resection involves the resection of the primary lesion but also of the loco-regional lymph nodes.In the large retrospective study of the Global Group of esophageal cancer collaboration (WECC) involving 3,572 patients having had resection of the main tumor (60% adenocarcinomas, 40% squamous cell carcinomas), a high total number of resected lymph nodes has been shown to be an independent prognostic factor of improved survival after esophagectomy for esophageal or gastroesophageal junction cancer. The maximum survival at 5 years is modulated by the T classification: it is recommended to resect 10 lymph nodes for a "pT1" stage tumor (pathologic tumor stage 1), 20 for a "pT2" stage and at least 30 for a "pT3" / "T4" stage. This number is important in terms of staging, the decision of adjuvant treatments and prognostic. A recent European study showed that the average number of resected lymph nodes was 20. In addition, lymphatic drainage is variable according to the type and location of tumors, involving an adapted lymphadenectomy strategy to each situation.
Also in gastric cancer, a complete resection (R0) and adequate lymphadenectomy are predictive factors for healing and long-term survival. Lymphadenectomy is adapted to the type, stage and location of the primary lesion.
In the U.S., the National Cancer Network guidelines recommend a D2 lymphadenectomy or a minimum of 15 lymph nodes (Lymph Node, LN) recovered.However, most international guidelines consider the recovery of only 15 LNs is insufficient. A recent Korean study on more than 25,000 patients showed that the maximum survival advantage is observed by performing a lymphadenectomy with a minimum of 29 LNs recovered. The experience of Western surgeons is much less than that of surgeons in Asia, and it seems obvious that an intraoperative guidance method would be a major support for the decision making in real time and thus remove the current variability related to the level of experience of the surgeon.
In addition, oncology surgery includes in the vast majority of cases a resection of an segment of the digestive tract and requires the restoration of digestive continuity by simple anastomosis and/or by interposition of another intestinal segment.
This stage of the surgical procedure is critical, since any anastomotic leakage is burdened with a risk of complication sometimes lethal. The surgeon's experience, which allows him to evaluate visually the vascularization of the tissue to be anastomosed, is therefore fundamental to prevent the problems.
In esogastric surgery, anastomotic leaks are associated with increased postoperative morbidity, an extended stay in the Intensive Care Unit (ICU), a longer overall hospital stay,reduced quality of life and, in the context of cancer, shortened cancer-specific survival.
Several studies have identified risk factors for anastomotic leakage, such as chemoradiotherapy, surgical technique, smoking, diabetes, and the location of the anastomosis. These factors may compromise the perfusion of the replacement conduit after esophagectomy and gastrectomy and increase the risk of anastomotic leakage. Objective assessment of tissue perfusion could be an excellent tool to identify ischemia of the conduits and thus reduce the incidence of anastomotic leaks. A perfusion compromise of the proximal portion of the gastric conduit, used for the recovery of the digestive continuity after esophagectomy, has been identified as one of the risk factors of digestive fistula.
It is therefore obvious that at the present time, for curative cancer resection or reconstruction after esogastric resection surgery, the outcome of the treatment depends mainly on the surgeon's experience and perception of the surgical field.
Today, the development of specific fluorescence imaging devices enables the surgeons to visualize tumors and vascular and lymphatic structures. This technology is expected to increase the reproducibility of esogastric surgery and its results.
The proposed study is based on the hypothesis that Fluorescence Image Guided Surgery (FIGS) would improve the quality and reproducibility of esophageal and stomach oncology surgery (lymphadenectomy and complete resection), as well as to decrease the risk of anastomotic complications after resective surgery of the esophagus or part or all of the stomach (study of the vascularization).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer, Gastric Cancer
Keywords
Esophageal cancer, Gastric cancer, Lymphadenectomy, Complications, Anastomosis
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
NIR Fluorescence guided lymphadenectomy and anastomosis
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Near Infra-Red Fluorescence Guided Surgery
Intervention Description
ICG injection around tumor each four direction by endoscopy followed by NIR fluorescence guidance laparoscopic or robotic esophagectomy or gastrectomy
Primary Outcome Measure Information:
Title
Evaluation of the usefulness of ICG fluorescence to guide lymphadenectomy in oncological esogastric resections
Description
Additional detection (YES-NO) of lymph nodes after activation of the NIR fluorescence guidance system during lymphadenectomy.
Time Frame
During the surgical procedure
Secondary Outcome Measure Information:
Title
Evaluation of the impact of fluorescence guidance on the number of resected lymph nodes in oncological esogastric resections
Description
Number of lymph nodes, counted in anatomopathological analysis, obtained after fluorescence-guided lymphadenectomy in the esogastric oncology resections compared to historical data
Time Frame
7 days after operation when pathologic result was reported
Title
Evaluation of the impact of fluorescence guidance in intraoperative evaluation of pre-anastomotic tissue perfusion
Description
Anastomotic fistula rate after fluorescence control of pre-anastomotic vascularisation in oncological esogastric resections compared to historical data
Time Frame
30 days after operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Man or woman over 18 years old.
Patient with resectable primitive esophageal or gastric cancer confirmed by biopsy without distant metastases
Patient with no contraindications to anaesthesia and performance of esophageal and/or gastric surgery
Patient able to receive and understand information related to the study and give written informed consent.
Patient affiliated to the French social security system.
Exclusion Criteria:
Patient undergoing emergency surgery (hemorrhage, occlusion or perforation).
Presence of distant metastasis
Patient at risk of allergy to indocyanine green or to other fluorescent compounds
Pregnant or lactating patient.
Patient in exclusion period (determined by a previous or a current study).
Patient under the protection of justice.
Patient under guardianship or trusteeship.
Patient deprived of liberty
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Armelle TAKEDA, PhD
Phone
+33 390413608
Email
armelle.takeda@ihu-strasbourg.eu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Silvana PERRETTA, MD, PhD
Organizational Affiliation
Service de Chirurgie Digestive et Endocrinienne, NHC, Strasbourg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Chirurgie Digestive et Endocrinienne, NHC
City
Strasbourg
ZIP/Postal Code
67000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Silvana PERRETTA, MD, PhD
Email
silvana.perretta@ircad.fr
12. IPD Sharing Statement
Plan to Share IPD
No
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Fluorescence Image Guided Foregut Surgery
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