Role of CTC´s Spread During Pancreaticoduodenectomy in Patients With Pancreatic and Periampullary Tumors (CETUPANC)
Primary Purpose
Pancreatic Tumor, Periampullary Carcinoma Resectable, Circulating Tumor Cells
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
No Touch (NT)
Superior Mesenteric Artery First (SMA)
Sponsored by
About this trial
This is an interventional other trial for Pancreatic Tumor
Eligibility Criteria
Inclusion Criteria:
1. Patients older than 18 years, with adenocarcinomas of the pancreas and potentially resectable periampullary tumors by cephalic duodenopancreatectomy or total duodenopancreatectomy indicated intraoperatively for technical reasons, who voluntarily agree to participate in the study and sign informed consent
Exclusion Criteria:
- Patients in whom liver metastases or peritoneal carcinomatosis are detected during surgery.
- Patients with neuroendocrine pancreatic tumors or cystic tumors.
- Patients in whom tumor resection is not finally achieved because it shows intraoperatively that the tumor is locally advanced and unresectable.
- Patients with macroscopic residual tumor (R2).
- High-risk patients with severe pathology (ASA IV) according to the American Association of Anesthesiologists.
- Patients receiving neoadjuvant therapy
- Patients in whom the intraoperative pathological anatomy indicates borders of pancreatic resection affected
Sites / Locations
- Hospital Universitario Virgen del Rocío
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
No Touch (NT)
Superior Mesenteric Artery First (SMA)
Arm Description
Pancreatic and Periampullary Tumors resection by no-touch technique
Pancreatic and Periampullary Tumors resection by superior Mesenteric Artery First technique
Outcomes
Primary Outcome Measures
Circulating tumor cells (CTC´s)
Change in the concentration of circulating tumor cells (CTCs) levels (nº CTCs/ mL blood) during the surgery, 4 blood samples will be taken from the portal vein
Local tumor recurrence
Presence (YES or NO) compatible images of local tumor recurrence Valid imaging tests of presence or absence can be checked by: computerized tomography (CT) or magnetic resonance (NMR)
Metastasis
Presence (YES or NO) compatible images of metastasis
Patient survival
Death (YES OR NO): number of patients dying during study
Secondary Outcome Measures
Morbidity
The complications evaluation and their severity will be based on the classification of Dindo-Clavien and the definitions of the International Study Group of Pancreatic Surgery (ISGPS).
Pancreatic fistula: Presence (yes or no) and degree (A, B, C)
Delayed gastric emptying: Presence (yes or no) and degree (A, B, C)
Hemorrhage: Presence (yes or no) and degree (A, B, C)
Full Information
NCT ID
NCT03340844
First Posted
October 16, 2017
Last Updated
October 14, 2021
Sponsor
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
1. Study Identification
Unique Protocol Identification Number
NCT03340844
Brief Title
Role of CTC´s Spread During Pancreaticoduodenectomy in Patients With Pancreatic and Periampullary Tumors
Acronym
CETUPANC
Official Title
Role of Circulating Tumor Cells (CTC´s) Spread During Pancreaticoduodenectomy in Metastasis and Survival Rates in Patients With Pancreatic and Periampullary Tumors
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 15, 2017 (Actual)
Primary Completion Date
July 15, 2023 (Anticipated)
Study Completion Date
July 15, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
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
This multicentre, prospective and randomized study aims(1:1) to compare the rate of recurrence, metastasis and survival according to the levels of intraoperative circulating tumor cells (CTCs) during cephalic duodenopancreatectomy in patients with pancreatic and periampullary tumors.
Detailed Description
Cephalic duodenopancreatectomy is the technique indicated for patients with pancreatic head carcinoma and periampullar tumors.
There are different technical variants, it is not standardized what is the best option in relation to local recurrence, metastasis and survival.
In the study, patients will be randomized into two study groups with pancreatic and periampullary tumors undergoing cephalic pancreatectomy (NT) vs initial approach by superior mesenteric artery (SMA).
The measurement of circulating tumor cells (CTCs) allows to assess the degree of cellular dissemination due to surgical manipulation.CTCs will be evaluated during surgery (nº CTCs / mL blood). To do this, a maximum of 4 blood samples from the portal vein will be performed, in each study group according to the following scheme:
NT group: basal (at the beginning of surgery), portal vein pancreatic detachment, postresection (NT2) and before closure (NT3).
SMA group: basal (at the beginning of surgery), after Kocher maneuver and SMA dissection, postresection, before closure.
Subsequently, the quantified levels of CTCs will be correlated with the occurrence of local tumor recurrence, metastasis development and patient patient survival.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Tumor, Periampullary Carcinoma Resectable, Circulating Tumor Cells, Metastasis
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, randomized (1:1) to 2 study groups according to duodenopancreatectomy surgical approach: "No-Touch group" (NT) or "Artery First group" (SMA) in patients with pancreatic and periampullary tumors, to evaluated circulating tumor cells (CTCs) levels during the surgery. Sample size = 86
Masking
None (Open Label)
Allocation
Randomized
Enrollment
86 (Actual)
8. Arms, Groups, and Interventions
Arm Title
No Touch (NT)
Arm Type
Experimental
Arm Description
Pancreatic and Periampullary Tumors resection by no-touch technique
Arm Title
Superior Mesenteric Artery First (SMA)
Arm Type
Active Comparator
Arm Description
Pancreatic and Periampullary Tumors resection by superior Mesenteric Artery First technique
Intervention Type
Procedure
Intervention Name(s)
No Touch (NT)
Intervention Description
Tumor resection by No-touch technique: dissection of hepatic hilum, dissection of superior mesenteric vein (SMV) in caudal aspect of pancreas, section of antrum, pancreatic neck section. Section-ligation of veins of duodenopancreatectomy part of SMV and portal. Then Kocher-uncrossing maneuver of the jejunal loop and final section of the retro-portal (back of the portal vein) blade.
Intervention Type
Procedure
Intervention Name(s)
Superior Mesenteric Artery First (SMA)
Intervention Description
Tumor resection by SMA technique: Kocher maneuver extends to the left renal vein (LRV). Dissection above the LRV of the SMA (refer to vessel-loop). Then, SMA will be identified on the caudal side of the pancreas (mesenterial root) and progressive dissection until its origin in the aorta artery (previously referenced with vessel loop).
Primary Outcome Measure Information:
Title
Circulating tumor cells (CTC´s)
Description
Change in the concentration of circulating tumor cells (CTCs) levels (nº CTCs/ mL blood) during the surgery, 4 blood samples will be taken from the portal vein
Time Frame
During the surgery: at the beginning of surgery, immediately after disconnecting the pancreas from the portal vein, just at the moment the pancreatic resection ends and before the skin closed
Title
Local tumor recurrence
Description
Presence (YES or NO) compatible images of local tumor recurrence Valid imaging tests of presence or absence can be checked by: computerized tomography (CT) or magnetic resonance (NMR)
Time Frame
From the day of surgery to 3 years of follow-up
Title
Metastasis
Description
Presence (YES or NO) compatible images of metastasis
Time Frame
From the day of surgery to 3 years of follow-up
Title
Patient survival
Description
Death (YES OR NO): number of patients dying during study
Time Frame
From the day of surgery to 3 years of follow-up
Secondary Outcome Measure Information:
Title
Morbidity
Description
The complications evaluation and their severity will be based on the classification of Dindo-Clavien and the definitions of the International Study Group of Pancreatic Surgery (ISGPS).
Pancreatic fistula: Presence (yes or no) and degree (A, B, C)
Delayed gastric emptying: Presence (yes or no) and degree (A, B, C)
Hemorrhage: Presence (yes or no) and degree (A, B, C)
Time Frame
From the day of surgery up to 6 weeks of follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1. Patients older than 18 years, with adenocarcinomas of the pancreas and potentially resectable periampullary tumors by cephalic duodenopancreatectomy or total duodenopancreatectomy indicated intraoperatively for technical reasons, who voluntarily agree to participate in the study and sign informed consent
Exclusion Criteria:
Patients in whom liver metastases or peritoneal carcinomatosis are detected during surgery.
Patients with neuroendocrine pancreatic tumors or cystic tumors.
Patients in whom tumor resection is not finally achieved because it shows intraoperatively that the tumor is locally advanced and unresectable.
Patients with macroscopic residual tumor (R2).
High-risk patients with severe pathology (ASA IV) according to the American Association of Anesthesiologists.
Patients receiving neoadjuvant therapy
Patients in whom the intraoperative pathological anatomy indicates borders of pancreatic resection affected
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco Javier Padillo Ruiz, PhD
Organizational Affiliation
Hospitales Universitarios Virgen del Rocío
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Virgen del Rocío
City
Sevilla
ZIP/Postal Code
41013
Country
Spain
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Yes. Anonymized data for individual participant data (IPD) is planned to be shared with all participants within 6 months of data completion
IPD Sharing Time Frame
Within 6 months after database closure and analysis.
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Role of CTC´s Spread During Pancreaticoduodenectomy in Patients With Pancreatic and Periampullary Tumors
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