Prophylactic Cholecystectomy in Midgut NETs Patients Who Require Primary Tumor Surgery. (TNE-IDC-COLE)
Primary Purpose
Midgut Carcinoid Tumor, Biliary Stones
Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Primary tumor surgery
Primary tumor surgery (bowel resection) combined with prophylactic cholecystectomy
Sponsored by
About this trial
This is an interventional treatment trial for Midgut Carcinoid Tumor focused on measuring Neuroendocrine tumor, prophylactic cholecystectomy, Biliary stone disease
Eligibility Criteria
Inclusion Criteria:
- Patients must grant the informed consent written, signed and dated.
- Male or female older than 18 years old.
- Radiological or histological diagnose of midgut NET that can be treated with surgery.
- In case of female with childbearing age (time between menarche and menopause), a pregnancy test with negative result.
- Neuroendocrine tumors located in any of the aforementioned locations.
- Presence or not of distant metastasis.
- Presencié or not of gallstones.
- Capacity of follow up.
Exclusion Criteria:
- Neuroendocrine tumors which are not located in jejunum or ileum (bronchial, gastric, pancreatic, descending colon, sigma or rectum.).
- Patients that have gone through a previous bowel resection.
- Patients with previous cholecystectomy.
- Pacients with biliary stone disease.
- Patients who are candidate to liver resection or liver transplant.
- Patients with a gallbladder polyp bigger than 6 mm.
- Pacients with one gallbladder sessile polyp, presence of more than one polyp or patients older than 50 years old with a polyp.
- Refusal to participate.
- Patients with previous history of malignant neoplasms in the last 5 years, except skin basal cell carcinoma, "in situ" cervical carcinoma or in situ carcinoma found in a polyp removed with a colonoscopy.
- Medical criteria that doesn't consider the patient a candidate to participate in the study.
Sites / Locations
- Hospital Universitari Trias i Pujol
- Instituto Catalán de Oncología
- IDIBELL, Hospital Universitari de Bellvitge.Recruiting
- Hospital del Mar
- Hospital Universitari Vall d'Hebron
- Hospital Universitario Gregorio Marañón
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Experimental group
Control group
Arm Description
Patients with midgut neuroendocrine tumor who will undergo only primary tumor surgery.
Patients with midgut neuroendocrine tumor that will undergo through primary tumor surgery combined with prophylactic cholecystectomy.
Outcomes
Primary Outcome Measures
To evaluate the rate of biliary stone disease associated to patients with midgut NET that have gone through primary tumor surgery.
Incidence of biliary stone disease in patients with midgut NET who requiere primary tumor surgery
Secondary Outcome Measures
To assess the incidence of post-operative complications until day 28 +/- 3 (1 Month) after the surgery.
Postoperative complications according Clavien-Dindo classification
To assess the incidence of: anastomotic dehiscence, wound infection, reoperation.
Specific complications
To evaluate the incidence of gallstone in patients who require a bowel resection and/or ileocecal junction resection.
choledochal lithiasis or cholelithiasis
To evaluate de incidence of gallstones in patients who will receive medical treatment with SSA
choledochal lithiasis or cholelithiasis according medical treatment
To describe bowel movements of patients after the surgery.
Gastrointestinal Quality of Life Index (GIQLY);Minimum value of 0 (the worst health state) and a maximum of 100 (best health state)
To compare quality of life in patients who went through a prophylactic cholecystectomy against those who did not.
Health related Quality of life 15 D (HRQoL 15D);There are 15 areas with a minimum value of 0 (the worst health state) and a maximum of 100 (best health state) 15D
Full Information
NCT ID
NCT04735198
First Posted
January 21, 2021
Last Updated
July 6, 2022
Sponsor
Hospital Universitari de Bellvitge
1. Study Identification
Unique Protocol Identification Number
NCT04735198
Brief Title
Prophylactic Cholecystectomy in Midgut NETs Patients Who Require Primary Tumor Surgery.
Acronym
TNE-IDC-COLE
Official Title
Effectiveness of Prophylactic Cholecystectomy in Patients With Midgut Neuroendocrine Tumor (Jejunum, Ileum or Proximal Colon) Who Require Primary Tumor Surgery. Randomized, Proof of Concept Clinical Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 20, 2021 (Actual)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
April 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari de Bellvitge
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
The investigators want to study the effectiveness of prophylactic cholecystectomy in patients with midgut neuroendocrine tumor (jejunum, ileum or proximal colon) who require primary tumor surgery. When patients are diagnosed and are tributary to surgical treatment, the tumor might compromise vascularization, and patients need an extensive bowel resection. The patients might also receive medical treatment with somatostatin analogs. The combination of extensive bowel resection and medical treatment might increase gallbladder stones, but patients might not develop biliary stone disease, as in the general population, where 20% of the population have gallbladder stones but only a 10 to 15 % of the population will develop symptoms.
The idea comes from the lack of literature about the incidence of biliary Stone disease in patients with midgut NET tumors.
It's a multicentric, open-label and randomized clinical trial to evaluate the incidence of biliary stone disease in patients with midgut NET who require primary tumor surgery combined or not to cholecystectomy.
Our hypothesis suggests that patients with midgut neuroendocrine tumor who require primary tumor resection without the combination of prophylactic cholecystectomy do not have an increased incidence of biliary stone disease two years after the surgery, regardless of treatment with SSA.
Detailed Description
Title: Effectiveness of prophylactic cholecystectomy in patients with midgut neuroendocrine tumor (jejunum, ileum or proximal colon) who require primary tumor surgery. Randomized, proof of concept clinical trial.
Background: The prevalence of midgut NET has increased due to advances in diagnostic tests and its indolent course. When patients are diagnosed, they might be tributary to surgical treatment requiring an extensive bowel resection, and medical treatment with somatostatin analogs. Both treatments are related with gallbladder stone formation. The ENETS and NANETs recommend prophylactic cholecystectomy in patients with midgut NET who require primary tumor surgery, However, there is a lack of scientific evidence reinforcing this recommendation.
Objectives: The main objective is to evaluate the cumulated incidence rate of biliary stone disease in patients with midgut NET who require primary tumor resection, two years after the surgery.
Design: It's a multicentric, open-label and randomized clinical trial. Patients will be recruited from the General Surgery Services of the six Hospitals participating in the study. Patients must fullfill inclusion and exclusion criteria.
It is expected to recruit a maximum of one hundred patients in two years (50 per group). Patients will be randomly assigned into the Experimental group (primary tumor resections) or Control group (primary tumor resections combined with cholecystectomy). The investigators will follow up patients until week 104 after surgery (8 visits).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Midgut Carcinoid Tumor, Biliary Stones
Keywords
Neuroendocrine tumor, prophylactic cholecystectomy, Biliary stone disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental group
Arm Type
Active Comparator
Arm Description
Patients with midgut neuroendocrine tumor who will undergo only primary tumor surgery.
Arm Title
Control group
Arm Type
Experimental
Arm Description
Patients with midgut neuroendocrine tumor that will undergo through primary tumor surgery combined with prophylactic cholecystectomy.
Intervention Type
Procedure
Intervention Name(s)
Primary tumor surgery
Other Intervention Name(s)
Bowel resection
Intervention Description
Large bowel resection.
Intervention Type
Procedure
Intervention Name(s)
Primary tumor surgery (bowel resection) combined with prophylactic cholecystectomy
Other Intervention Name(s)
prophylactic cholecystectomy.
Intervention Description
Large bowel resection combined and cholecystectomy.
Primary Outcome Measure Information:
Title
To evaluate the rate of biliary stone disease associated to patients with midgut NET that have gone through primary tumor surgery.
Description
Incidence of biliary stone disease in patients with midgut NET who requiere primary tumor surgery
Time Frame
Two years after the surgery
Secondary Outcome Measure Information:
Title
To assess the incidence of post-operative complications until day 28 +/- 3 (1 Month) after the surgery.
Description
Postoperative complications according Clavien-Dindo classification
Time Frame
One month after the surgery
Title
To assess the incidence of: anastomotic dehiscence, wound infection, reoperation.
Description
Specific complications
Time Frame
One month after the surgery
Title
To evaluate the incidence of gallstone in patients who require a bowel resection and/or ileocecal junction resection.
Description
choledochal lithiasis or cholelithiasis
Time Frame
Two years after the surgery
Title
To evaluate de incidence of gallstones in patients who will receive medical treatment with SSA
Description
choledochal lithiasis or cholelithiasis according medical treatment
Time Frame
Two years after the surgery
Title
To describe bowel movements of patients after the surgery.
Description
Gastrointestinal Quality of Life Index (GIQLY);Minimum value of 0 (the worst health state) and a maximum of 100 (best health state)
Time Frame
Two years after the surgery
Title
To compare quality of life in patients who went through a prophylactic cholecystectomy against those who did not.
Description
Health related Quality of life 15 D (HRQoL 15D);There are 15 areas with a minimum value of 0 (the worst health state) and a maximum of 100 (best health state) 15D
Time Frame
Two years after the surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients must grant the informed consent written, signed and dated.
Male or female older than 18 years old.
Radiological or histological diagnose of midgut NET that can be treated with surgery.
In case of female with childbearing age (time between menarche and menopause), a pregnancy test with negative result.
Neuroendocrine tumors located in any of the aforementioned locations.
Presence or not of distant metastasis.
Presencié or not of gallstones.
Capacity of follow up.
Exclusion Criteria:
Neuroendocrine tumors which are not located in jejunum or ileum (bronchial, gastric, pancreatic, descending colon, sigma or rectum.).
Patients that have gone through a previous bowel resection.
Patients with previous cholecystectomy.
Pacients with biliary stone disease.
Patients who are candidate to liver resection or liver transplant.
Patients with a gallbladder polyp bigger than 6 mm.
Pacients with one gallbladder sessile polyp, presence of more than one polyp or patients older than 50 years old with a polyp.
Refusal to participate.
Patients with previous history of malignant neoplasms in the last 5 years, except skin basal cell carcinoma, "in situ" cervical carcinoma or in situ carcinoma found in a polyp removed with a colonoscopy.
Medical criteria that doesn't consider the patient a candidate to participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Inés Ginot
Phone
696014147
Email
inesginot@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ricardo Frago Montanuy
Organizational Affiliation
Hospital Universitari de Bellvitge
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitari Trias i Pujol
City
Badalona
State/Province
Barcelona
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra Vela
Email
sandravela1@gmail.com
Facility Name
Instituto Catalán de Oncología
City
L'Hospitalet De Llobregat
State/Province
Barcelona
Country
Spain
Individual Site Status
Active, not recruiting
Facility Name
IDIBELL, Hospital Universitari de Bellvitge.
City
Barcelona
ZIP/Postal Code
08907
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Inés Ginot
Phone
696014147
Email
inesginot@gmail.com
Facility Name
Hospital del Mar
City
Barcelona
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joan Altet
Email
joanaltet@gmail.com
First Name & Middle Initial & Last Name & Degree
Joan Altet
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
José Luís Sánchez
Email
30208jsg@comb.cat
Facility Name
Hospital Universitario Gregorio Marañón
City
Madrid
Country
Spain
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luís Miguel Jiménez
Email
luismijg@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
That's not decided yet
Learn more about this trial
Prophylactic Cholecystectomy in Midgut NETs Patients Who Require Primary Tumor Surgery.
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