Clinical Research Directory

Inclusion Criteria: * Adults ≥18 years of age with the ability to independently provide written informed consent, fulfilling the criteria for either the oncology or control cohort, capable of undergoing baseline BALF and peripheral blood sampling at treatment commencement or time of diagnosis, and consenting to serial blood sampling at 2-4 weeks and 8-12 weeks following treatment initiation. Exclusion Criteria: 1. Active infection or established non-drug-related etiology of ILD (including but not limited to connective tissue disease-associated ILD, environmental or occupational exposure-induced ILD, active radiation pneumonitis) 2. Prolonged pre-enrollment treatment with moderate-to-high dose systemic corticosteroids or immunosuppressive agents that would compromise baseline evaluation 3. Absolute contraindications to bronchoscopic procedures or inability to comply with scheduled key follow-up assessments 4. Severe decompensated comorbid conditions 5. Pregnancy or lactation period.