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The Canada Lymph Node Score Project: A Crossover Trial

Phase 3
Completed
Conditions
Lung Cancer
Non-small Cell Lung Cancer Stage I
Non-small Cell Lung Cancer Stage II
Non Small Cell Lung Cancer
Interventions
Diagnostic Test: Systematic Sampling
Diagnostic Test: Selective Targeted Sampling
Registration Number
NCT04342377
Lead Sponsor
St. Joseph's Healthcare Hamilton
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Systematic SamplingSystematic SamplingUpon 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.
Selective Targeted SamplingSelective Targeted SamplingDuring 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.
Primary Outcome Measures
NameTimeMethod
Non-Inferiority Margin between Selective Targeted Sampling and Systematic Sampling2 years

A margin of 5% or less would be considered satisfactory for STS to be deemed non-inferior to SS.

Secondary Outcome Measures
NameTimeMethod
Agreement (between staging methods)2 years

Based on Cohen's Kappa statistics

Difference in Procedure Length2 years

For each sampling method (in minutes)

Diagnostic Statistics (between staging methods)2 years

Sensitivity, specificity, negative predictive value and positive predictive value

Inconclusive Biopsy Rate2 years

Percentage of lymph nodes with inconclusive pathology from biopsy

Diagnostic Yield (accuracy)2 years

Proportion of lymph nodes with a pathological diagnosis for both sampling methods

Difference in Cost per Procedure2 years

For each sampling method (sum of dollar costs for EBUS procedure)

Trial Locations

Locations (7)

McMaster University

🇨🇦

Hamilton, Ontario, Canada

Health Sciences Centre

🇨🇦

Winnipeg, Manitoba, Canada

Toronto General Hospital

🇨🇦

Toronto, Ontario, Canada

Royal Alexandra Hospital

🇨🇦

Edmonton, Alberta, Canada

CHUM Endoscopic Tracheo-bronchial and Oesophageal Center

🇨🇦

Montréal, Quebec, Canada

MUHC Interventional Pulmonology Department

🇨🇦

Montréal, Quebec, Canada

St. Joseph's Healthcare Hamilton

🇨🇦

Hamilton, Ontario, Canada

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