Plasma MTB cfDNA Before Bronchoscopy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChinese University of Hong Kong

About this trial

Tuberculosis (TB) remains a major global health challenge, affecting over 10 million people annually. Hong Kong carries an intermediate TB burden, with \~3,200 new cases reported yearly. Pulmonary TB (PTB), the most common form, presents diagnostic difficulties. Traditional methods like sputum smear and culture often fail in patients unable to produce adequate samples, necessitating bronchoscopy to collect bronchoalveolar lavage (BAL) for mycobacterial testing.

These limitations pose risks for patients and strain healthcare systems. Bronchoscopy is invasive, resource-intensive, and may delay treatment-especially for elderly patients with comorbidities. Blood-based inflammatory markers lack diagnostic specificity. A rapid, non-invasive alternative is urgently needed.

The investigators developed a plasma-based assay that detects Mycobacterium tuberculosis cell-free DNA (MTB cfDNA) in blood. This liquid biopsy leverages metagenomic sequencing and computational analysis to identify TB-specific genetic material while minimizing contamination. Preliminary data show excellent diagnostic performance, with area under the receiver operating characteristic curve values \>0.94 for TB pleurisy.

The investigators propose a prospective clinical validation study comparing plasma MTB cfDNA testing to bronchoscopy with BAL culture and molecular testing. The primary aim is to demonstrate non-inferiority of plasma cfDNA within a 10% sensitivity margin. Secondary aims include assessing how clinical and radiological features affect test performance and evaluating the assay's ability to detect drug resistance mutations for personalized therapy.

Validation could transform TB diagnosis by offering a rapid, safe, and accurate blood test. Patients could avoid invasive procedures, receive faster diagnoses, and begin treatment sooner. Detecting resistance mutations directly from plasma would enable timely, targeted therapy-critical for addressing multidrug-resistant TB. This represents a paradigm shift toward precision medicine in TB care.

Tailored to Hong Kong's epidemiological context, this study addresses a key diagnostic gap. The approach has global relevance, with potential to improve clinical outcomes, reduce costs, and accelerate progress toward WHO's TB elimination goals.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18 years or above

Presence of respiratory indication requiring bronchoscopy

Sputum AFB smear negative or unable to expectorate sputum for investigations

Disqualifiers

BALF collected but not sent for MTB PCR

History of PTB or EPTB

Concomitant use of at least two anti-TB medications for more than 14 consecutive days in the past 3 months

Repeated bronchoscopy in the same subject within the study period

Trial population

Patients with clinical indications for undergoing bronchoscopy and BAL who meet the inclusion and exclusion criteria will be prospectively enrolled in consecutive sequences

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Diagnostic Test: Plasma MTB cfDNA assay

    Diagnostic test

    Quantitative measurement of MTB cfDNA level in the plasma

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: PTB1 intervention
Group B: Non-PTB1 intervention

Trial outcomes

Primary outcomes

1

Area under ROC curve of MTB cfDNA assay

The area under ROC curve of MTB cfDNA assay in discriminating PTB and non-PTB in a prospective non-selective cohort of bronchoscopy procedures

Time frame
27 months

Secondary outcomes

1

The effect of radiological features on the diagnostic performance (sensitivity and specificity) of the MTB cfDNA assay

To compare the diagnostic performance (sensitivity and specificity) of the MTB cfDNA assay in patients with different radiological features (cavitary vs non-cavitary)

Time frame
27 months

Other outcomes

Sponsors and contacts

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