Lung Cancer Clinical Trial
Official title:
Microbiome in Patients With Pulmonary Tuberculosis, Non-tuberculous Mycobacterial Pulmonary Diseases (NTM-PD), Lung Cancer and Hemoptysis
Microbiome in lower respiratory diseases is not sufficiently known yet. The objective of this study is to investigate microbiome in patients who present with hemoptysis, and those with pulmonary tuberculosis, non-tuberculous mycobacterial pulmonary disease (NTM-PD), and lung cancer, analyzing respiratory specimen acquired by bronchoscopic approach.
Subjects who were going to undergo bronchoscopy for hemoptysis or suspected lower respiratory
diseases including endobronchial tuberculosis (Tb), NTM-PD, or endobronchial lung cancer (LC)
were enrolled after informed consents.
Subjects who were supposed to receive bronchoscopy to rule out endobronchial lesions were
also enrolled as control group (ctrl) after informed consents. In those control group,
endobronchial tuberculosis, malignancy or other certain respiratory diseases was not clearly
suspected.
Before acquiring respiratory specimens, bronchoscopic channels were washed to acquire
negative control in all cases of groups.
In Tb group and LC group, specimens of normal bronchial mucosa near suspicious endobronchial
lesion were obtained with protected brush (PB), then specimens of abnormal bronchial mucosa
in suspicious endobronchial lesion with PB. After acquiring respiratory specimens of PB,
bronchial washing was done in suspicious endobronchial lesion.
In NTM-PD group, specimens of bronchial mucosa in bronchus of suspicious NTM-PD with PB.
After acquiring respiratory specimens of PB, bronchial washing was done in bronchus of
suspicious NTM-PD.
In hemoptysis group, bronchial washing was done in bronchus of ongoing bleeding.
In control group, specimens of bronchial mucosa in predetermined random bronchus (not
bronchus with suspicious endobronchial lesion) with PB. After acquiring respiratory specimens
of PB, bronchial washing was done in the same bronchus.
Microbiome in lower respiratory species was analyzed using 16S rRNA sequencing.
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