EBUS Score Validation for Malignancy

Sponsor
McMaster University (Other)
Overall Status
Completed
CT.gov ID
NCT02793713
Collaborator
Toronto General Hospital (Other), Vancouver General Hospital (Other)
300
2
15.5
150
9.7

Study Details

Study Description

Brief Summary

Surgical removal of a tumour in the lung offers the best chance for survival in early stage lung cancers. One main criteria of surgical eligibility is the absence of cancer spread to the lymph nodes; rendering the staging process extremely important. The evaluation of these lymph nodes is thought to be best completed using Endobronchial Ultrasound (EBUS), a procedure in which several lymph nodes are sampled and send to pathology to determine whether or not it is malignant. More recently, studies have observed that there are clear differences in the characteristics of cancerous and benign (non-cancerous) lymph nodes, and so there has been great interest in creating a list of criteria that can determine whether a node is malignant. This study aims to prospectively validate a previously proposed score based on observed characteristics of lymph nodes during an EBUS procedure relating to pathology-confirmed results. To test this, the results of the lymph node samples and the observed score will be compared for agreement. If the investigators find that the scoring system can accurately predict which lymph nodes are cancerous, it would provide the evidence to establish the score as a standard procedure during cancer staging.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endobronchial Ultrasound

Study Design

Study Type:
Observational
Actual Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Validation of a Malignancy Scoring System During Endoscopic Evaluation of Mediastinal Lymph Nodes for Lung Cancer
Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Sep 17, 2017
Actual Study Completion Date :
Sep 17, 2017

Outcome Measures

Primary Outcome Measures

  1. Internal validity of an aggregate sonographic score [Duration of EBUS procedure (estimated 1 hour)]

    Objective is to compare the lymph node malignancy predictor score obtained by two raters, one who performed the procedure and the other a secondary rater who viewed the video of the procedure. The score will ideally be similar between raters, showing good inter-rater internal validity.

  2. External validity of an aggregate sonographic score [From time of EBUS procedure to date of surgery (expected to be up to 1 month)]

    As the gold standard for lymph node assessment is via tissue sampling obtained during an EBUS (or other invasive method) procedure, the scores obtained using the lymph node malignancy predictor scoring technique will be compared to later post-surgical pathological staging. The score will be considered to have good criterion (external) validity if there is a high degree of agreement between the pathology and score values.

Secondary Outcome Measures

  1. Rate of staging re-intervention after initial EBUS [Up to 12 months]

    If the original tissue samples taken during the EBUS procedure were found to be insufficient to rule out malignancy, the patient may undergo another EBUS, or will undergo an Endoscopic ultrasound or a mediastinoscopy. During these follow-up procedures, the surgeon would be obtaining additional tissue in the hope that a result can be made. These re-intervention is not without a risk of adverse events, and ideally should be minimized. We will be abstracting re-intervention occurrences from patient charts.

  2. Correlation between lymph node aggregate sonographic score and Positron Emission Tomography-elicited Standardized Uptake Values (SUVs) [From first presentation for diagnosis to date of surgery (Estimated to be 2-3 months)]

    All patients undergo Positron Emission Tomography in the course of their clinical staging for suspected lung cancer. The values obtained from this diagnostic test (Standardized Uptake Values [SUVs]) will be obtained and compared to the surgeon's observed score on the lymph node aggregate sonographic scoring tool to investigate whether there is any relationship between the score and the SUVs.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Must be diagnosed with confirmed or suspected lung cancer and be undergoing EBUS diagnosis/staging
Exclusion Criteria:
  • N/A

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Joseph's Healthcare Hamilton Hamilton Ontario Canada L8N 4A6
2 Toronto General Hospital Toronto Ontario Canada M5G 2C4

Sponsors and Collaborators

  • McMaster University
  • Toronto General Hospital
  • Vancouver General Hospital

Investigators

  • Principal Investigator: Wael C Hanna, MDCM MBA, McMaster University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
McMaster University
ClinicalTrials.gov Identifier:
NCT02793713
Other Study ID Numbers:
  • EBUS_ScoreValidation
First Posted:
Jun 8, 2016
Last Update Posted:
Feb 14, 2018
Last Verified:
Feb 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by McMaster University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2018