Lung Cancer Clinical Trial
Official title:
Additive Value of EBUS TBNA for Staging Non-Small Cell Lung Cancer in Patients Evaluated for Stereotactic Body Radiation Therapy
This clinical trial studies how well endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) after positron emission tomography/computed tomography (PET/CT) scan works in diagnosing patients with stage I-IIA non-small cell lung cancer evaluated for stereotactic body radiation therapy (SBRT). Performing EBUS-TBNA after PET/CT scan may help doctors learn more about the accuracy and ways to find early stage lung cancer.
PRIMARY OBJECTIVES: I. To assess the use of EBUS-TBNA after a PET/CT as a means of improving the accuracy of lymph node staging in patients considered for SBRT. SECONDARY OBJECTIVES: I. To assess the usefulness of PET/CT as a diagnostic test in identifying N1 versus N0 staging. II. To compare survival and recurrence rates in patients with discordant PET/CT and EBUS-TBNA. III. To describe EBUS-TBNA and SBRT related complications. OUTLINE: Patients undergo EBUS-TBNA before SBRT. After completion of study, patients are followed up at 6 weeks, then every 3 months for the first 2 years then twice a year for the following 3 years, and annually thereafter. ;
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