EUS vs. MDCT in Pancreatic Malignancy

Resectable Pancreatic Cancer Clinical Trial

— EUSPACT  

Official title:

Endoscopic UltraSound in Potentially Resectable PAncreatic Malignancy - Does it Bear the Weight of the Rapidly Evolving Technology of Computer Tomography?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02115022
• Other study ID #: Col-gastro 5
• Status: Completed
• Start date: July 2014
• Est. completion date: February 2018

Study information

• Verified date: April 2020
• Source: Clinical Hospital Colentina
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Accurate staging of patients with pancreatic cancer is critical to avoid the expense, morbidity, and mortality related to unnecessary surgery. While several tests are available for assessing such patients, consensus has not been achieved on the optimal approach. As a matter of fact, pancreatic cancer staging is discussed controversially due to conflicting evidence and certainly EUS has lost grounds due to improvements in CT technology. Thus, the role of EUS and EUS-guided FNA varies among treatment centers.

The present study is designed to better define the role of EUS in predicting resectability, as compared to high resolution cross-sectional imaging.

Description:

Registry procedures:

• HIGH-RESOLUTION PANCREATIC PROTOCOL COMPUTED TOMOGRAPHY (CT) SCAN EXAMINATION: performed on at least 16-section multi-detector row (MD) CT and reviewed using multi-planar reconstructions, with images obtained following the oral administration of water and pancreatic protocol intravenous iopamidol, with images acquired in the pancreatic and portal venous phases of contrast enhancement, reconstructed as thin slice (at 1 mm - pancreatic phase or 2 mm - portal venous phase increments).

• EUS EXAMINATION: performed within 2 weeks of the MDCT, aiming visualization of the pancreas, main surrounding vascular structures, celiac and mediastinal lymph nodes, liver and left adrenal gland, with EUS-FNA performed at the discretion of the investigator/examiner to confirm/exclude metastases and for the confirmation of malignancy in the primary tumor. Patients confirmed by EUS as having distant metastases are to be deferred from the planned surgical intervention.

• SURGICAL INTERVENTION: aiming to provide curative intent (R0) resection.

• HISTOPATHOLOGICAL POSTOPERATIVE STAGING: with evaluation of loco-regional invasiveness and degree of complete surgical resection (R0/R1).

• FOLLOW-UP OF PATIENTS: with phone-calls on an every 6 month basis, for up to 2 years, retaining the following data: survival (or not), date of decease and its direct cause (if applicable), the presence of tumor recurrence (or not).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: February 2018
• Est. primary completion date: January 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• adult (= 18 years of age) patients;

• the presence of a confirmed pancreatic mass (suspected neoplastic) deemed resectable or borderline resectable on multislice (at least 16 simultaneously acquired slices) pancreatic protocol computed tomography (CT);

• patients fit and willing to undergo surgery with a curative (R0) intent;

• sign of the informed consent.

Exclusion Criteria:

• the presence of significant co-morbidities that contraindicate pancreatic resection;

• previous neo-adjuvant oncologic therapy;

• distant metastases;

• lack of discernment;

• refusal to sign the informed consent..

Related Conditions & MeSH terms

• Pancreatic Neoplasms
• Resectable Pancreatic Cancer

Locations

Country	Name	City	State
Romania	Fundeni Clinical Institute	Bucharest
Romania	Gastroenterology Department, Clinical Hospital Colentina	Bucharest
Romania	University Military Hospital	Bucharest
Romania	Iuliu Hatieganu University of Medicine	Cluj Napoca
Romania	Research Center in Gastroenterogy and Hepatology	Craiova	Dolj

Sponsors (4)

Lead Sponsor	Collaborator
Clinical Hospital Colentina	Institutul Clinic Fundeni, Iuliu Hatieganu University of Medicine and Pharmacy, University of Medicine and Pharmacy Craiova

Country where clinical trial is conducted

Romania, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Staging capability of each study procedure	Each imaging test (MDCT and EUS) and findings at or after surgery are to be judged on their ability to provide descriptions of the primary tumor's size, location, relationship to vessels - using the terms abutment (=180º of contact) and encasement (>180º of contact), vessel occlusion, variant vascular anatomy, a grade regarding local tumor resectability (resectable, borderline resectable, or locally advanced; R0 or R1 resection), and extent and location of extrapancreatic disease.	Up to 2 weeks, depending on the time of the surgical intervention
Secondary	Side-effects related to the EUS examination	Each patient will be monitored for 24 hours after the EUS examination to identify possible early complications of the procedure	Monitored for 24 hours after EUS
Secondary	Patient survival time, and tumor recurrence-free survival	Each patient is going to be followed-up for up to 2 years after the surgical intervention an an every-6 month basis, in order to identify events such as death or tumor recurrence.	Up to 2 years