Malignant pleural or pericardial effusion is common in lung cancer, and intrapleural drugs injection is important in the treatment. Non- cytotoxic drugs include those with a sclerosing effect that produces pleurodesis, which is easy to cause severe chest pain despite of no influence on the following chemotherapy. Tumor angiogenesis is important in producing MPE. Bevacizumab has been administrated locally in treating optic nerve sickness successfully by anti-VEGF mechanism. So we hypothesize that intrapleural bevacizumab is also effective in treating MPE.
Inclusion Criteria: 1. Histological or cytological diagnosis of non-small cell lung cancer. 2. Cytological diagnosis of malignant pleural or pericardial effusion (MPE) 3. Symptomatic MPE evaluated by researchers 4. Unsuitable for or reject systemic therapy of tumor 5. Continuous TKI treatment after TKI-resistance 6. Estimated survival of more than 3 months. 7.18 years or older Exclusion Criteria: 1. Current or recent (within 10 days prior to treatment) use the full amount of inhibition of platelet function, anticoagulants or thrombolytic therapy, which allows prophylactic anticoagulants 2. Be allergic to bevacizumab 3. Pregnant or lactating woman 4. Pleural or pericardial infection
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
22
Bevacizumab 100 mg, intrapleural injection treating MPE after the drainage of MPE
The First Affliliated Hospital of Guangzhou MC
Guangzhou, Guangdong, China
Lung cancer symptom
Time frame: Evaluated by lung cancer symptom scale 21-30 days after the treatment
response rate
Time frame: Evaluate response rate 21-30 days after the treatment
Time to progression
Time frame: 1 year after the treatment of MPE.
Overall survival
Time frame: 1 year after the treatment of MPE
Number of Participants with Adverse Events
Time frame: one months after the treatment of MPE
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