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Completed

NCT Number: NCT04342377

The Canada Lymph Node Score Project: A Crossover Trial

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Royal Alexandra Hospital, Edmonton, Alberta, Canada

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Selective Targeted Sampling

Diagnostic Test

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.

Other names: STS

Systematic Sampling

Diagnostic Test

All examined mediastinal lymph nodes are biopsied, regardless of whether they appear normal during PET, CT and EBUS.

Other names: SS

Primary outcomes

  1. Non-Inferiority Margin between Selective Targeted Sampling and Systematic Sampling

    Time frame: 2 years

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

Secondary outcomes

  1. Diagnostic Statistics (between staging methods)

    Time frame: 2 years

    Sensitivity, specificity, negative predictive value and positive predictive value

  2. Agreement (between staging methods)

    Time frame: 2 years

    Based on Cohen's Kappa statistics

  3. Inconclusive Biopsy Rate

    Time frame: 2 years

    Percentage of lymph nodes with inconclusive pathology from biopsy

  4. Diagnostic Yield (accuracy)

    Time frame: 2 years

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

  5. Difference in Procedure Length

    Time frame: 2 years

    For each sampling method (in minutes)

  6. Difference in Cost per Procedure

    Time frame: 2 years

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

Sponsors and collaborators

Lead sponsor

St. Joseph's Healthcare Hamilton

Other

Collaborators

  • Centre hospitalier de l'Université de Montréal (CHUM)
  • Health Sciences Centre, Winnipeg, Manitoba
  • McGill University Health Centre/Research Institute of the McGill University Health Centre
  • Royal Alexandra Hospital
  • Toronto General Hospital

Registry information

Official study title

Improving Preoperative Lung Cancer Staging Through the Canada Lymph Node Project: A Pan-Canadian Multicentered Crossover Trial

Acronym: CLNS

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Apr 13, 2020
Registry last updated
Jul 27, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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