Impact of Preoperative Endoscopic Ultrasound-guided Fine-needle Aspiration in Cholangiocarcinoma Patients

Last updated: July 30, 2024
Sponsor: Asian Institute of Gastroenterology, India
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Abdominal Cancer

Biliary Tract Cancer

Liver Cancer

Treatment

Endoscopic ultrasound-guided fine-needle aspiration

Clinical Study ID

NCT06534229
ROSC01
  • Ages 18-75
  • All Genders

Study Summary

Primary objective of this study is to evaluate the number of patients with positive LN detected by EUS and precluded from further surgical interventions.

Secondary objective of this study is to evaluate the EUS-related adverse events.

Eligibility Criteria

Inclusion

Inclusion Criteria:

In order to be eligible to participate in this study, a patient must meet the following criteria:

  • Suspected resectable CCA

  • Patient underwent EUS preoperatively

Exclusion

Exclusion Criteria:

A patient who meets any of the following criteria will be excluded from inclusion:

• History of treated CCA

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: Endoscopic ultrasound-guided fine-needle aspiration
Phase:
Study Start date:
August 25, 2024
Estimated Completion Date:
August 25, 2026

Study Description

Cholangiocarcinoma (CCA) is a rare malignancy originating from the bile duct epithelium. The incidence of CCA ranges from 0.5-2.5 cases per 100.000 people in West-European countries and 1.6 cases per 100.000 people in the United States of America. CCA is classified based on anatomical site and is divided into intrahepatic (iCCA), perihilar (pCCA) and distal (dCCA). Survival is limited, as CCA is often recognized in a relatively late stadium in which potential curative treatment is not an option anymore.

Currently, surgical resection is the only potentially curative treatment. The resectability of CCA depends on multiple factors: e.g. biliary extension, vascular involvement and presence of metastatic disease. Patients with metastatic disease, including both distant lymph nodes and metastases, are ineligible for surgical resection and palliative treatment should be initiated instead. Therefore, correct lymph node (N) staging is crucial. N staging depends on CCA subtype and differs between the 7th and 8th edition of The American Joint Committee on Cancer (AJCC) staging system. The most important difference between the two staging systems is the location of the regional (N1) versus distant lymph nodes (N2) in the 7th edition for pCCA and dCCA, while in the 8th edition distant N locations are considered M1 metastases and the number of lymph nodes determines the N stage. In both editions N locations in iCCA are subdivided for the left and right sided liver segments.The AJCC staging system is used to determine treatment and is correlated to survival. The 5-year survival for patients with regional or non-regional positive lymph nodes is worse compared to patients with negative lymph nodes.

To identify distant and lymph node metastases Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) is performed. However, it is difficult to accurately identify suspicious lymph nodes on both CT and MRI since sensitivity and specificity is 61% and 88% respectively for CT and 64% and 68% respectively for MRI. To assess lymph node staging more accurately, Endoscopic Ultrasound (EUS) with Fine Needle Aspiration (FNA) might be of added value. Only a few retrospective studies have described the yield of preoperative EUS for CCA. It is clear that EUS is an effective technique for lymph node staging for CCA, but data is inconsistent about the exact value and impact of EUS on clinical decision making.

Connect with a study center

  • AIG Hospitals

    Hyderabad, Telangana 500032
    India

    Site Not Available

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