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Study Comparing EBUS & EUS to Mediastinoscopy in Staging and Detection of Lung Cancer

Not Applicable
Terminated
Conditions
Non Small Cell Lung Cancer
Interventions
Procedure: Mediastinoscopy/thoracoscopy
Procedure: EBUS/EUS
Registration Number
NCT00970645
Lead Sponsor
Mayo Clinic
Brief Summary

This is a prospective randomized clinical trial with the study cohort comprised of all male and female patients over the age of 21 presenting to the study site for evaluation of lung cancer. The study will enroll 300 subjects, with 150 in each arm. Three sites will be in the study, Mayo Rochester, Mayo Jacksonville and Medical University of South Carolina. Mayo Rochester will enroll approximately 125 subjects. This study does not require subjects to undergo any additional procedures than what they would receive per standard medical care. The consenting subjects will receive EUS and /or EBUS- guided FNA or Mediastinoscopy/Thoracoscopy.

Detailed Description

This is a prospective randomized clinical trial of males and females age 21 or older being evaluated for lung cancer. The study will enroll approximately 300 subjects (150 in each arm) at 3 participating centers (MUSC, Mayo Clinic Rochester and Jacksonville). This sample size will provide sufficient statistical power (i.e. \>80%) using a non-inferiority study design with 1-sided hypothesis testing (Farrington and Manning 1990) to determine whether or not the sensitivity of the EUS/EBUS diagnostic technique is inferior (i.e. 10% or more lower) when compared to the sensitivity of malignant mediastinal adenopathy of about 40%. This study requires subjects to agree to the selection of their standard of care procedure. Subjects will be randomized (stratified computer generated randomization stratified y center and y CT positivity for pathologically enlarged \[\>1cm short axis\] node - 10 strata). Randomization will use variable block sizes (4-8), so that randomization allocation remains concealed as investigators will not be blinded. This study requires subjects to consent to the release of outcome data and follow-up data to be used for study analysis. No additional visit will be required for this study; this study will not require any additional time requirements beyond their scheduled evaluations.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
2
Inclusion Criteria
  • Age 21 years or greater
  • Pt is a surgical candidate for mediastinoscopy, thoracoscopy, or lung resection
  • Known or suspected non-small cell carcinoma of the lung eligible for resection
  • CT scan performed within 45 days prior to evaluation for study participation
  • PET scan performed within 45 days prior to evaluation for study participation
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Exclusion Criteria
  • Pathologically proven metastatic disease
  • History of malignancy within 5 years other than (skin) basal cell carcinoma
  • Enlarged ipsilateral mediastinal lymph nodes > 2.5 cm in diameter
  • Peripheral T1 tumors with normal mediastinal lymph nodes on CT and PET
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
traditional mediastinoscopy/thoracoscopyMediastinoscopy/thoracoscopyTraditional Mediastinoscopy used to detect or stage lung cancers.
EBUS/EUSEBUS/EUSMinimal invasive technique for staging/detecting lung cancer.
Primary Outcome Measures
NameTimeMethod
Develop an integrated staging technique to detect early metastases in lung cancer which should affect patient outcomes more accurately than conventional staging techniques.Post operative
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

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