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CompletedNCT01329575CT0024Updated Mar 30, 2018

Predicting Malignancy Using Endoluminal Ultrasound Characteristics in Mediastinal Lymph Nodes

An observational study in Neoplasm of Mediastinal Lymph Nodes, sponsored by Centre hospitalier de l'Université de Montréal (CHUM). Completed at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-03-30.

Sponsored by Centre hospitalier de l'Université de Montréal (CHUM) · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
184
Ages
18 Years and older
Sex
All
01

Study summary

There is no single method to investigate mediastinal LN invasion. Hence, a patient may have to undergo several tests and procedures. Noninvasive and invasive approaches are employed. Within the invasive techniques, endoscopic ultrasonography with needle aspiration (EUS-FNA) and endobronchial ultrasonography with transbronchial needle aspiration (EBUS-TBNA) are gaining importance in mediastinal staging.5 They provide ultrasonographic images and permit needle aspiration under direct vision for cytology specimen analysis. As more evidence is being accumulated on these staging approaches, the number of cervical mediastinoscopies, considered as the gold-standard for mediastinal staging, is diminishing.

Color Doppler LN characteristics with endoluminal ultrasound (US) is only mentioned in a small number of studies and needs to be further investigated.13,14 With the good results obtained with superficial US, it seems reasonable to believe that color Doppler characteristics would increase accuracy in detecting malignancy of mediastinal LNs with endoluminal US.

Read the detailed description

Lung cancer is the leading cause of cancer-related death in the United States with a 5-year survival rate of 15,7%.1 In lung cancer and other malignancies, such as esophageal cancer, accurate staging is essential to establish prognosis and for patient management. Staging will help determine if surgery, chemotherapy, radiation therapy, a combination of these, or a palliative approach is the most adequate.2,3

Assessment of lymph nodes (LNs) for invasion by metastasis is undertaken if patient management is influenced by a positive or negative result. In non-small cell lung cancer (NSCLC), mediastinal LN invasion by malignant cells is a critical factor to determine if a patient is considered as a surgical candidate or not.2 In esophageal cancer, LN metastasis may be found in the mediastinum, the neck and the abdomen.4 Invasion of these LNs must be considered in the selection of treatment of esophageal cancer.3,4

There is no single method to investigate mediastinal LN invasion. Hence, a patient may have to undergo several tests and procedures. Noninvasive and invasive approaches are employed. Within the invasive techniques, endoscopic ultrasonography with needle aspiration (EUS-FNA) and endobronchial ultrasonography with transbronchial needle aspiration (EBUS-TBNA) are gaining importance in mediastinal staging.5 They provide ultrasonographic images and permit needle aspiration under direct vision for cytology specimen analysis. As more evidence is being accumulated on these staging approaches, the number of cervical mediastinoscopies, considered as the gold-standard for mediastinal staging, is diminishing.6

Characteristics of benign and malignant LNs using ultrasonography have been described in various contexts. Cervical and axillary LNs provided accurate characteristics (eg. shape, short- to long-axis ratio, number of blood vessels in LN, vascularization pattern, etc.) in predicting malignancy with linear superficial transducers.7-11 LN characteristics using EUS or EBUS also have established criteria predicting mediastinal LN malignancy (eg. size, shape, borders and echogenicity).12 Depending on the studies, it has been suggested to obtain specimens of all accessible LNs without considering their characteristics. It has also been suggested to proceed to a selective LN aspiration based on LN characteristics, with the advantage of cost reduction (fewer needles used, less time to carry out procedure, and specimens needed to be analysed).6

Color Doppler LN characteristics with endoluminal ultrasound (US) is only mentioned in a small number of studies and needs to be further investigated.13,14 With the good results obtained with superficial US, it seems reasonable to believe that color Doppler characteristics would increase accuracy in detecting malignancy of mediastinal LNs with endoluminal US.

New processors and probes are more accurate than the ones used in some of the past studies. Hence, the investigators can possibly obtain more precise findings than the ones the investigators can find in the literature.14

This study will consist of a prospective assessment of LN characteristics in patients undergoing EUS-FNA and/or EBUS-TBNA for diagnostic purposes. Cytology results will be considered as the gold-standard. By comparing the LN characteristics with the cytology results, the investigators will establish a scoring system to accurately predict malignancy.

The impact of this study is significant. If clinicians can accurately predict malignancy in mediastinal lymph nodes using ultrasound characteristics, biopsy of these lymph nodes could be avoided which would decrease the risk to the patient and the cost to the system (disposable needle costs, cytological preparation and analysis).

Hypotheses:

With a combination of endoluminal ultrasound characteristics, a simple scoring system can be established to help predict malignancy in mediastinal lymph nodes.

Objectives:

  1. Establish a scoring system to accurately predict mediastinal lymph node malignancy with endoluminal ultrasound.
  2. Retrospectively evaluate the impact of the established scoring system on the number of lymph nodes aspirations required for accurate staging.

Study Design:

Prospective, cohort study design. Clinical trial: Intervention - endoluminal ultrasound.

Methods:

This study will consist of a prospective non-randomized evaluation of endoluminal ultrasound characteristics in mediastinal lymph nodes using endoluminal ultrasound to predict malignancy within these nodes. All patients undergoing EUS-FNA and/or EBUS-TBNA for mediastinal LN staging for any suspected or confirmed malignancy at the CHUM - Hôpital Notre-Dame will be approached in an attempt to enroll them in the study. Patients will be enrolled and consented for the study during the pre-operative evaluation in the pre-operative clinic. The investigators will aim to recruit 100 consecutive patients.

Consented patients will undergo EUS with or without FNA and/or EBUS with or without TBNA in the same way as planned or decided during the procedure by the surgeon. During the procedure, data will be collected, including lymph node size, shape, border, echogenicity, homogeneity, location, color Doppler characteristics, number of nodes, etc. This will not add additional steps or time to the procedure. All this data and the cytology results obtained from EUS-FNA and EBUS-TBNA will be entered in a prospective database.

The cytology results will be considered as the gold-standard and with the collected characteristics univariate and multivariate logistic regressions will be used to establish a scoring system to predict malignancy. Sensitivity, specificity, positive predictive value, negative predictive value and accuracy will be determined based on the developed model.

02

Conditions studied

  • Neoplasm of Mediastinal Lymph Nodes

Keywords

  • endoluminal ultrasound
  • Mediastinal LN invasion
03

In context

Lead sponsor

Centre hospitalier de l'Université de Montréal (CHUM) is the lead sponsor of 376 studies on the registry; 110 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Primary care clinic

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients undergoing EUS-FNA and/or EBUS-TBNA for mediastinal LN assessment

Exclusion criteria

Exclusion Criteria:

  • Age \< 18 years old
  • Inability to consent to the study
  • Medications including Warfarin (Coumadin) or Clopidogrel (Plavix)
  • Coagulopathy
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
184 participants (actual)
06

What researchers measure

Primary outcomes

  1. With a combination of endoluminal ultrasound characteristics, a simple scoring system can be established to help predict malignancy in mediastinal lymph nodes.

    collected characteristics univariate and multivariate logistic regressions will be used to establish a scoring system to predict malignancy. Sensitivity, specificity, positive predictive value, negative predictive value and accuracy will be determined based on the developed model.

    Time frame: 3 months

07

Study locations

1 site
  • Centre Hospitalier de l'Université de Montréal
    Montreal, Quebec H2L 4M1, Canada
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2011, a primary completion of Dec 2016 and a completion of Jul 2017. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 4, 2011
First posted
Apr 6, 2011
Start
Jan 2011
Primary completionActual
Dec 2016
CompletionActual
Jul 2017
Last update
Mar 30, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 30, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01329575
Collaborators
Centre de Recherche du Centre Hospitalier de l'Université de Montréal
Responsible party
Sponsor
First posted
Apr 6, 2011
Start date
Jan 2011
Primary completion
Dec 2016
Completion
Jul 2017
Last update
Mar 30, 2018

Study contacts

Moishe Liberman, MD, PhD
principal investigator · Centre hospitalier de l'Université de Montréal (CHUM)

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2018. You cannot join it, but the record below documents what was studied.

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