Clinical Research Directory

Inclusion Criteria: 1. Informed consent has been signed, and according to the judgment of the investigator, the patient can comply with the study protocol and sign the written informed consent; 2. NSCLC patients who have been clinically diagnosed with RP or CIP after histopathologically confirmed radiotherapy or immunocheckpoint inhibitor treatment and have not received glucocorticoid or other drugs. 3. ≥18 years old, less than 75 years old; 4. ECOG PS score 0-3 in the Eastern Tumor Collaboration group; 5. Patients without contraindications to alveolar lavage; Exclusion Criteria: 1. Poor patient compliance and violation of test regulations; 2. Liver and kidney dysfunction, such as myocardial infarction, angina pectoris, liver transaminase significantly increased; 3. Had any medical condition requiring systemic treatment with corticosteroids or other immunosuppressive drugs within 14 days prior to enrollment; 4. Severe infection occurred within 4 weeks prior to enrollment, including but not limited to hospitalization due to infection complications, bacteremia or severe pneumonia; 5. Severe chronic or active infections (including tuberculosis infection) requiring systemic (oral or intravenous) antibiotic treatment within 14 days prior to enrollment; 6. Untreated patients with chronic hepatitis B, HBV carriers with HBV DNA≥ 500 IU/mL, or patients with active hepatitis C virus (HCV) should be excluded. Note: Non-active hepatitis B, surface antigen (HBsAg) carriers, treated and stable hepatitis B carriers (HBV DNA \& LT; 500 IU/mL), patients with cured hepatitis C could be enrolled; 7. Known history of HIV infection; 8. Received any other investigational drug or participated in any other clinical trial within 28 days.