About this trial
This study intends to carry out prospective, randomized controlled clinical trials in many centers across the country to compare the efficacy and safety of immunotherapy after standard first-line chemotherapy or immunotherapy combined with interventional bronchial artery chemoembolization for stage IV lung squamous cell carcinoma.
Eligibility criteria
Qualifiers
Squamous cell carcinoma of the lung confirmed by histology or cytology;
According to the TNM staging system of the 9th edition of American Cancer Association, it was assessed as stage IV.
Has received standard first-line chemotherapy immunotherapy for 4~6 cycles, and achieved partial remission or disease stability according to the efficacy evaluation of RECIST1.1;
The patient is 18-80 years old;
Disqualifiers
There is epidermal growth factor receptor (EGFR) sensitive mutation or anaplasticlymphomakinase (ALK) gene translocation;
Have a history of allergy to contrast agents or chemotherapy drugs;
Received other anti-tumor treatments other than standard first-line chemotherapy immunotherapy;
Arrhythmia with myocardial ischemia or myocardial infarction above grade II and poor control (including QTc interval ≥450ms for men and ≥ 470 ms for women);
Trial design
Treatments tested in this trial
- Immunotherapy combined with interventional therapy group
- Immunotherapy group