Efficacy and Safety of First-line Anti-PD-1/PD-L1 Monoclonal Antibody in Combination With Chemotherapy and Bronchoscopy-assisted Interventional Therapy in Patients With Advanced Central Non-small Cell Lung Cancer

Korábbi kezelés

• Patients with contraindications to chemotherapy or immunotherapy.
• Patients have received a live vaccines within 28 days of the first drug use. Patients receiving inactivated viral vaccines to treat seasonal influenza are allowed, but inactivated live influenza vaccines with intracn nasal drugs are not allowed.

Más betegség

• Patients have other active malignancies. Patients with cured limited tumors, such as skin substrate cell carcinoma, skin squamous cancer, superficial bladder cancer, carcinoma in situ of prostate, carcinoma in situ of cervix, and breast in-place cancer, can be included.
• Patients with human immunodeficiency virus (HIV) infection.
• Patients with infection of active tuberculosis.
• Patients have a known history of psychosophedic substance abuse or drug abuse;

Egyéb

• Patients with uncertain diagnosis.
• Non-central NSCLC patients.
• Bronchoscopy is contraindicated in patients.
• Pregnant or lactating women.
• The researchers determined that there may be other factors that might have contributed to the early termination of the study.

• Patients volunteer to participate in clinical studies and sign an informed consent (ICF), and are willing to follow and able to complete all trial procedures.
  • 2)18-75 years of age 3) All patients included are diagnosed with lung cancer detected by fibrous bronchoscope or percutaneous lung puncture biopsy, and are confirmed as NSCLC by Immunohistochemistry.
• Obstruction-type central lung cancer that cannot be surgically removed. 5) Patients without EGFR, ALK, and ROS mutation. 6) Patients have not previously received systemic treatment for phase IV NSCLC or patients receiving the adjuvant or neoadjuvant therapy for more than 6 months before the diagnosis of phase IV NSCLC.
• Within 4 weeks, at least one measurable lesions are required for researchers to evaluate in accordance with RECIST 1.1 requirements.
• Appropriate tumor tissues for PD-L1 expression level determination are required.
• Relevant laboratory tests indicate tolerance for chemotherapy, immunotherapy, and bronchoscopy.