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Intrapleural Bevacizumab Injection for Malignant Effusion in Lung Cancer

Intrapleural Bevacizumab Injection for Treating Malignant Pleural or Pericardial Effusion in Non-small Cell Lung Cancer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02054052
Enrollment
22
Registered
2014-02-04
Start date
2014-01-31
Completion date
2019-03-31
Last updated
2019-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Pleural Effusion, Non-small Cell Lung Cancer

Keywords

non-small cell lung cancer, malignant pleural effusion, bevacizumab, intrapleural injection, pericardial effusion

Brief summary

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.

Detailed description

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

Interventions

DRUGBevacizumab

Bevacizumab 100 mg, intrapleural injection treating MPE after the drainage of MPE

Sponsors

Haihong Yang, MD, Pricipal investigator
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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. Estimated survival of more than 3 months. 6.18 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

Design outcomes

Primary

MeasureTime frame
Lung cancer symptomEvaluated by lung cancer symptom scale 21-30 days after the treatment

Secondary

MeasureTime frame
response rateEvaluate response rate 21-30 days after the treatment
Time to progression1 year after the treatment of MPE.
Overall survival1 year after the treatment of MPE
Number of Participants with Adverse Eventsone months after the treatment of MPE

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026