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Endoscopic Ultrasound Versus Endoscopic Retrograde Cholangiopancreatography (ERCP) Tissue Sampling for the Diagnosis of Suspected Pancreatico-Biliary Cancer

C

California Pacific Medical Center Research Institute

Status

Completed

Conditions

Pancreaticobiliary Cancers
Jaundice
Bile Duct Obstruction

Treatments

Procedure: EUS FNA
Procedure: ERCP

Study type

Interventional

Funder types

Other

Identifiers

NCT01356030
2011.048

Details and patient eligibility

About

The two most commonly used methods to biopsy suspected pancreaticobiliary masses are (1) endoscopic ultrasound guided fine-needle aspiration (EUS-FNA) and (2) cytology brush biopsies obtained during endoscopic retrograde cholangiopancreatography (ERCP). At most centers, the specific method used depends on the availability of the technology and local expertise. Although it is believed that EUS-FNA is more accurate than ERCP brushings, there have been no head-to-head comparisons. The investigators' hypothesis is that EUS-FNA is superior to ERCP in obtaining tissue biopsies of pancreaticobiliary tumors, and the investigators aim to directly compare the two techniques.

Full description

Patients with pancreaticobiliary tumors usually present with painless jaundice due to bile duct obstruction. The standard clinical evaluation may include EUS and/or ERCP. At centers where EUS is available (like CPMC), it is usually used first as it is generally considered a better tool for tumor detection, staging, and performing biopsies (FNA). ERCP is then performed, if needed, to place a stent and relieve jaundice. As EUS is a relatively newer technology that has not widely disseminated, other centers use ERCP as the 1st modality to evaluate suspected malignant pancreaticobiliary obstruction. The role of ERCP in this setting is to not only place a stent to relieve jaundice, but to additionally obtain cytology brushings for tissue diagnosis.

Several studies have reported high sensitivity of EUS-FNA for detecting pancreaticobiliary cancers that are causing bile duct obstruction and jaundice (80-90%). The sensitivity for ERCP brushings and biopsies to detect the same types of tumors is reportedly lower (30-80%), but there have been no direct comparisons of these techniques.

Few centers use both technologies (EUS and ERCP) for patient care, or often perform EUS and ERCP at separate sessions. At CPMC, the investigators routinely perform EUS and ERCP together for patients needing these procedures. Thus the investigators are in a unique position to directly compare EUS-FNA to ERCP brushings for tissue diagnosis of suspected pancreaticobiliary tumors.

The proposed study will be the 1st direct comparison of EUS-FNA to ERCP tissue sampling for patients with suspected pancreaticobiliary cancers. Study results will highlight the best approach to obtain a biopsy diagnosis of pancreatic and biliary tract cancers.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients age >18 years that are scheduled for EUS and possible ERCP for the evaluation of jaundice from suspected pancreaticobiliary tumors.

Exclusion criteria

  • Patients that do not provide consent for EUS and ERCP (for standard clinical reasons)

  • Patients that do not require ERCP based on EUS findings (e.g. no mass seen, mass is not causing jaundice

  • Patients in whom an additional 5 minutes of procedure time may increase the procedural/sedation risks:

    • pregnant patients
    • patients with severe medical co-morbidities (ASA class 4 or 5)
  • Patients with significant bleeding risk precluding endoscopic tissue sampling

    • INR > 1.4 or Prothrombin time > 5 sec more than control
    • Platelet count < 50,000

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

51 participants in 2 patient groups

EUS-FNA
Active Comparator group
Treatment:
Procedure: EUS FNA
ERCP Brushing and Biopsy
Active Comparator group
Treatment:
Procedure: ERCP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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