Skip to main content
Clinical Trials/NCT03435588
NCT03435588
Completed
Not Applicable

Endoscopic Ultrasound (EUS)-Guided Fine Needle Aspiration (FNA) With Rapid On-site Evaluation (ROSE) of Cytopathology vs. EUS-guided Fine Needle Biopsy (FNB) Alone in the Diagnosis of Pancreatic Solid Lesions: a Randomized Controlled Trial

McGill University Health Centre/Research Institute of the McGill University Health Centre6 sites in 1 country235 target enrollmentFebruary 14, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Solid Pancreatic Tumor
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Enrollment
235
Locations
6
Primary Endpoint
Diagnostic accuracy
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Currently, the best way to evaluate pancreatic masses is through endoscopic-guided needle sampling of the mass to determine the diagnosis by looking at the acquired tissue under a microscope. This is done by inserting a small camera (endoscope) through the mouth of the patient then advanced to the stomach and using ultrasound guidance a sample of the pancreas can be acquired through the stomach. The sampling is usually done with a small needle called fine needle aspiration needle or FNA. FNA alone is sometimes limited due to inadequate acquisition of cells for proper diagnosis under the microscope, which can lead to need for repeat endoscopic procedures and delay in diagnosis and possibly treatment. Rapid on-site evaluation of cytopathology (ROSE) is where a cytopathologist is next to the physician doing the endoscopic procedures and evaluates each sampling performed immediately under the microscope and can give feedback to the endoscopist until enough cells has been acquired for a diagnosis. This method has been shown to increase the ability to diagnose pancreatic cancer but is expensive and requires significant amount of resources. New needles called core needles (fine needle biopsy, FNB) have recently been developed which not only acquires cells but also the entire tissue structure (histology) and has been shown to be also very accurate in the diagnosis of pancreatic cancer.

The purpose of this study is to compare endoscopy-guided biopsy of pancreatic masses with the new core needle (FNB), which can obtain more tissue for diagnosis vs. using a traditional needle (FNA) with the help of an immediate assessment of the obtained samples under the microscope to determine whether enough tissue has been obtained (ROSE). Both approaches have been shown to increase the accuracy of diagnosis in solid pancreatic masses but it is unclear which one is superior. This is a randomized trial meaning that the participants would either undergo biopsy with the new needle or with the traditional needle plus the addition of on-site assessment of the obtained samples. The advantage of the new needle is that it is easy to implement and likely much cheaper. If the investigators can show in our study that the new needles are as accurate as FNA with ROSE then FNB could be implemented across hospitals worldwide in an easier and less expensive fashion.

Registry
clinicaltrials.gov
Start Date
February 14, 2018
End Date
December 15, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
Responsible Party
Principal Investigator
Principal Investigator

Yen-I Chen

Assistant Professor of Medicine, Division of Gastroenterology and Hepatology

McGill University Health Centre/Research Institute of the McGill University Health Centre

Eligibility Criteria

Inclusion Criteria

  • Age \> 18 years
  • Patients referred for EUS evaluation of a definite solid pancreatic mass noted on computed tomography(CT)/Magnetic resonance imaging(MRI)/EUS, in which malignancy is suspected with no previous histological diagnosis

Exclusion Criteria

  • Age \< 18 years, pregnant patients.
  • Uncorrectable coagulopathy Prothrombin time (PT) \>50% of control, Partial Thromboplastin time (PTT) \>50 sec, or International normalized ratio (INR) \>1.5 and/or uncorrectable thrombocytopenia platelet count\<50, 000109/L.

Outcomes

Primary Outcomes

Diagnostic accuracy

Time Frame: 12 months

Defined as (true positive + true negative)/all samples

Final diagnosis of malignant pancreatic mass

Time Frame: 10 months

Will be based on the following criteria: * Histological evidence of malignancy on the corresponding subsequent surgical specimen * Presence of an unresectable lesion during subsequent surgery * Malignant cytology/pathology on EUS-sampling followed by documented loco-regional progression/development of metastases on follow-up axial imaging.

Final diagnosis of benign pancreatic mass

Time Frame: 10 months

Will be based on the following criteria: * Surgical pathology or exploration showing the absence of malignancy * Follow-up imaging at \> 6 months reporting stability of the pancreatic lesion * Cytological or histopathological diagnosis of benign disease with an appropriate clinical course of disease for minimum of 6 months

Secondary Outcomes

  • Procedural time(6 to 12 months of data collection and 3 to 6 months of data analysis.)
  • Rate of procedure-related adverse events(6 to 12 months of data collection and 3 to 6 months of data analysis.)
  • Diagnostic characteristics(6 to 12 months of data collection and 3 to 6 months of data analysis.)
  • Median number of needle passes(6 to 12 months of data collection and 3 to 6 months of data analysis.)
  • Specimen adequacy(6 to 12 months of data collection and 3 to 6 months of data analysis.)

Study Sites (6)

Loading locations...

Similar Trials