Malignant Hydrothorax, Non Small Cell Lung Cancer
Conditions
Brief summary
The purpose of this multi-center clinical trial is to verify more effective on local control of malignant pleural effusions in NSCLC patients by thoracic cavity perfusion of recombinant human adenovirus type 5 injection and recombinant human Endostatin injection (Endostar) compared with cisplatin perfusion, with acceptable side effects.
Detailed description
Malignant pleural effusion, which can malfunction of circulatory and respiratory systems, is a common complication in advanced NSCLC, finally decreases the quality of life and lifespan. Nowadays, it is still a challenge to effectively control malignant pleural effusion. In this multi-center randomized and controlled clinical trial, 134 NSCLC patients diagnosed as malignant pleural effusion in the first time will enroll. Based on systemic chemotherapy and pleural cavity perfusion, all eligible patients are randomly assigned into treatment group (recombinant human adenovirus type 5 and Endostatin injections) and control group (cisplatin) with ratio 1:1. Local control rate and side effects are record respectively. The anticipation is that treatment group obtains faster and longer control of pleural effusion.
Interventions
Sponsors
Xinqiao Hospital of Chongqing
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. age 18-75 yrs; 2. Kamofsky score (KPS) ≥70, and a predicted lifespan \>3 months; 3. Enough function of vital organs, such as heart, liver and kidney; 4. Advanced NSCLC diagnosed by cytology or pathology 5. Unilateral or bilateral of malignant pleural effusion in the first time; 6. Patients who are considered as malignant pleural effusion by cytology or biomarkers (CEA, CA199, CA125) in pleural effusion; 7. Without systemic infection or high fever; 8. Without active EGFR mutation or unwilling to targeted molecular therapy; 9. NO Anti tumor Radiotherapy chemotherapy and molecular targeted therapy,or Received Anti tumor Radiotherapy chemotherapy and molecular and clinical remission more than three months and in the past month ,disease progress with pleural cavity effusion but haven't use systemic or local anti tumor treatment. 10. No pleural cavity injection of antineoplastic drugs.
Exclusion criteria
1. Non-malignant pleural effusion; 2. Pleural effusion cause by other malignant tumors; 3. Allergic to Recombinant human adenovirus type 5 injection or Endostar; 4. Pregnant or lactation women; 5. Previously using Medicine for treating NSCLC with pleural cavity effusion by Systemic or pleural cavity perfusion treatment one month prior to enrollment; 6. Previously using the diuretics, albumin and anti-angiogenesis drugs, or dexamethasone one month prior to enrollment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Objective response rate (ORR) of malignant pleural effusions | up to 3 years | Assessed by WHO Cancerous effusion scoring system |
Secondary
| Measure | Time frame |
|---|---|
| progression-free survival | up to 3 years |
Other
| Measure | Time frame | Description |
|---|---|---|
| quality of life | up to 3 years | Assessed by Karnofsky Performance Status(KPS) |
| side effects | up to 3 years | Assessed by NCI CTC3.0 |
Contacts
Primary ContactZhengTang Chen, PHD
Outcome results
None listed