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The Canada Lymph Node Score Project: A Crossover Trial (CLNS)

Primary Purpose

Lung Cancer, Non Small Cell Lung Cancer, Non-small Cell Lung Cancer Stage I

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Selective Targeted Sampling
Systematic Sampling
Sponsored by
St. Joseph's Healthcare Hamilton
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lung Cancer focused on measuring Mediastinal Staging, Nodal Disease, Endobronchial Ultrasound, Diagnostic Testing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years
  • Both CT and PET scans completed prior to EBUS
  • Suspected or confirmed NSCLC requiring mediastinal staging
  • cN0-cN1 as indicated by CT and PET scans

Exclusion Criteria:

  • Patients with cN0 disease AND peripheral tumors AND tumor < 2 cm in diameter, as they do not require mediastinal staging
  • Evidence of cN2 disease or higher on CT and PET scans

Sites / Locations

  • Royal Alexandra Hospital
  • Health Sciences Centre
  • St. Joseph's Healthcare Hamilton
  • McMaster University
  • Toronto General Hospital
  • CHUM Endoscopic Tracheo-bronchial and Oesophageal Center
  • MUHC Interventional Pulmonology Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Selective Targeted Sampling

Systematic Sampling

Arm Description

During patients' Endobronchial Ultrasound (EBUS) procedure, they will first undergo: Selective Targeted Sampling - endosonographic assessment of at least 3 mediastinal lymph node stations (4R, 4L, and 7) using the four criteria of the Canada Lymph Node Score (predictor of nodal disease during Endobronchial Ultrasound). Each lymph node will be assigned a CLNS ranging from 0 to 4. Triple Normal lymph nodes will be defined as those that appear normal on CT (diameter < 1 cm), AND normal on PET (SUV < 2.5), AND normal on EBUS (CLNS < 2). Lymph nodes that are found to be Triple Normal will be marked as "Not for Biopsy", whereas all other lymph nodes will be biopsied.

Upon completion of Systematic Targeted Sampling, all patients will crossover and receive the standard of care: Systematic Sampling - all lymph nodes previously marked as "Not for Biopsy" will be biopsied. At the conclusion of the EBUS procedure, all nodal stations would have been sampled as is mandated by current guidelines.

Outcomes

Primary Outcome Measures

Non-Inferiority Margin between Selective Targeted Sampling and Systematic Sampling
A margin of 5% or less would be considered satisfactory for STS to be deemed non-inferior to SS.

Secondary Outcome Measures

Diagnostic Statistics (between staging methods)
Sensitivity, specificity, negative predictive value and positive predictive value
Agreement (between staging methods)
Based on Cohen's Kappa statistics
Inconclusive Biopsy Rate
Percentage of lymph nodes with inconclusive pathology from biopsy
Diagnostic Yield (accuracy)
Proportion of lymph nodes with a pathological diagnosis for both sampling methods
Difference in Procedure Length
For each sampling method (in minutes)
Difference in Cost per Procedure
For each sampling method (sum of dollar costs for EBUS procedure)

Full Information

First Posted
April 8, 2020
Last Updated
July 25, 2022
Sponsor
St. Joseph's Healthcare Hamilton
Collaborators
Health Sciences Centre, Winnipeg, Manitoba, Royal Alexandra Hospital, Toronto General Hospital, Centre hospitalier de l'Université de Montréal (CHUM), McGill University Health Centre/Research Institute of the McGill University Health Centre
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1. Study Identification

Unique Protocol Identification Number
NCT04342377
Brief Title
The Canada Lymph Node Score Project: A Crossover Trial
Acronym
CLNS
Official Title
Improving Preoperative Lung Cancer Staging Through the Canada Lymph Node Project: A Pan-Canadian Multicentered Crossover Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
November 30, 2020 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Joseph's Healthcare Hamilton
Collaborators
Health Sciences Centre, Winnipeg, Manitoba, Royal Alexandra Hospital, Toronto General Hospital, Centre hospitalier de l'Université de Montréal (CHUM), McGill University Health Centre/Research Institute of the McGill University Health Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Before deciding on treatment for patients with lung cancer, a critical step in the investigation is finding out whether the lymph nodes in the chest contain cancer cells. This is accomplished with a biopsy of the lymph nodes through the airway wall, known as Endobronchial Ultrasound-guided Transbronchial Needle Aspiration. Guidelines require that every single lymph node in the chest be biopsied through a process called Systematic Sampling. However, emerging data suggests that the lymph nodes that appear benign on imaging and ultrasound do not need a biopsy. A proposed alternative to the inefficient Systematic Sampling is the simplified Selective Targeted Sampling of the lymph nodes, whereby only lymph nodes that look malignant are biopsied. This trial will evaluate the simplified Selective Targeted Sampling of lymph nodes and compare it to Systematic Sampling to see whether it is equally as effective in staging lung cancer.
Detailed Description
Treatment decisions in Non-Small Lung Cancer (NSCLC) are reliant on a thorough staging process that includes imaging with Computed Tomography (CT), Positron Emission Tomography (PET) and Systematic Sampling (SS) of mediastinal lymph nodes (LNs) by Endobronchial Ultrasound Transbronchial Needle Aspiration (EBUS-TBNA). Collectively, the results of these staging procedures dictate whether patients will be treated with surgery, radiation and/or chemotherapy. Current guidelines for SS through EBUS-TBNA mandate the biopsy of at least 3 mediastinal LN stations (4R, 4L and 7) in the chest, even if they appear normal on CT and PET scan. Despite improvements in diagnostic techniques and safety, LN biopsies remain onerous for the patient and costly to our healthcare system. SS is also unreliable, yielding inconclusive pathology results in 42.14% of cases, especially for Triple Normal LNs, which are LNs that appear normal on PET, and CT, and EBUS. In fact, SS results in mostly negative or inconclusive biopsies for Triple Normal LNs, which may be due in part to their very low probability (< 6%) of malignancy. As such, the researchers have proposed to replace the onerous and unreliable process of SS by a simpler Selective Targeted Sampling (STS) staging process. In STS, Triple Normal LNs will not be biopsied, due to the very high negative predictive value (NPV) of malignancy. STS follows the simple notion that only LNs that have the potential to be malignant should be biopsied, whereas LNs which are very likely benign (i.e. Triple Normal LNs) should not be biopsied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer, Non Small Cell Lung Cancer, Non-small Cell Lung Cancer Stage I, Non-small Cell Lung Cancer Stage II
Keywords
Mediastinal Staging, Nodal Disease, Endobronchial Ultrasound, Diagnostic Testing

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Model Description
A prospective pan-Canadian, multicentered, non-inferiority crossover study design
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Selective Targeted Sampling
Arm Type
Experimental
Arm Description
During patients' Endobronchial Ultrasound (EBUS) procedure, they will first undergo: Selective Targeted Sampling - endosonographic assessment of at least 3 mediastinal lymph node stations (4R, 4L, and 7) using the four criteria of the Canada Lymph Node Score (predictor of nodal disease during Endobronchial Ultrasound). Each lymph node will be assigned a CLNS ranging from 0 to 4. Triple Normal lymph nodes will be defined as those that appear normal on CT (diameter < 1 cm), AND normal on PET (SUV < 2.5), AND normal on EBUS (CLNS < 2). Lymph nodes that are found to be Triple Normal will be marked as "Not for Biopsy", whereas all other lymph nodes will be biopsied.
Arm Title
Systematic Sampling
Arm Type
Active Comparator
Arm Description
Upon completion of Systematic Targeted Sampling, all patients will crossover and receive the standard of care: Systematic Sampling - all lymph nodes previously marked as "Not for Biopsy" will be biopsied. At the conclusion of the EBUS procedure, all nodal stations would have been sampled as is mandated by current guidelines.
Intervention Type
Diagnostic Test
Intervention Name(s)
Selective Targeted Sampling
Other Intervention Name(s)
STS
Intervention Description
Mediastinal lymph nodes are assessed with the CLNS, and only those appearing malignant with the score are biopsied. Triple Normal lymph nodes (normal appearing on PET, CT and EBUS) are not biopsied.
Intervention Type
Diagnostic Test
Intervention Name(s)
Systematic Sampling
Other Intervention Name(s)
SS
Intervention Description
All examined mediastinal lymph nodes are biopsied, regardless of whether they appear normal during PET, CT and EBUS.
Primary Outcome Measure Information:
Title
Non-Inferiority Margin between Selective Targeted Sampling and Systematic Sampling
Description
A margin of 5% or less would be considered satisfactory for STS to be deemed non-inferior to SS.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Diagnostic Statistics (between staging methods)
Description
Sensitivity, specificity, negative predictive value and positive predictive value
Time Frame
2 years
Title
Agreement (between staging methods)
Description
Based on Cohen's Kappa statistics
Time Frame
2 years
Title
Inconclusive Biopsy Rate
Description
Percentage of lymph nodes with inconclusive pathology from biopsy
Time Frame
2 years
Title
Diagnostic Yield (accuracy)
Description
Proportion of lymph nodes with a pathological diagnosis for both sampling methods
Time Frame
2 years
Title
Difference in Procedure Length
Description
For each sampling method (in minutes)
Time Frame
2 years
Title
Difference in Cost per Procedure
Description
For each sampling method (sum of dollar costs for EBUS procedure)
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Both CT and PET scans completed prior to EBUS Suspected or confirmed NSCLC requiring mediastinal staging cN0-cN1 as indicated by CT and PET scans Exclusion Criteria: Patients with cN0 disease AND peripheral tumors AND tumor < 2 cm in diameter, as they do not require mediastinal staging Evidence of cN2 disease or higher on CT and PET scans
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Waël C Hanna, MDCM, MBA, FRCSC
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Alexandra Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T5H 3V9
Country
Canada
Facility Name
Health Sciences Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3A 1R9
Country
Canada
Facility Name
St. Joseph's Healthcare Hamilton
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Facility Name
McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 4L8
Country
Canada
Facility Name
Toronto General Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada
Facility Name
CHUM Endoscopic Tracheo-bronchial and Oesophageal Center
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2L 4M1
Country
Canada
Facility Name
MUHC Interventional Pulmonology Department
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H4A 3S9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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The Canada Lymph Node Score Project: A Crossover Trial

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