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Recruiting Phase 1, Phase 2 NCT05455034

Single-cell Sequencing of BLF to Guide the Treatment of Radiation Pneumonitis or Immune Checkpoint Inhibitor Pneumonitis

Trial Parameters

Condition Pneumonitis
Sponsor Xinqiao Hospital of Chongqing
Study Type INTERVENTIONAL
Phase Phase 1, Phase 2
Enrollment 40
Sex ALL
Min Age 18 Years
Max Age 80 Years
Start Date 2023-08-01
Completion 2025-12-30
Interventions
single-cell sequencing

Brief Summary

A multicenter, exploratory clinical research, to map the radiation or immune checkpoint inhibitor pneumonitis in patients with alveolar lavage single-celled map. Find out the pathogenesis and prevention strategies of radiation or immune checkpoint inhibitor pneumonitis. Specific treatment is given based on the recommendation of the treatment guidelines for radiation or immune checkpoint inhibitor pneumonitis and the results of single cell sequencing, which will become a new technology for clinical application.

Eligibility Criteria

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

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