Dry Pleurodesis With Talcum and Afatinib is Used to Treat Patients With Non-Small Cell Lung Carcinoma (DPTA)
Primary Purpose
Non Small Cell Lung Cancer
Status
Active
Phase
Phase 1
Locations
Georgia
Study Type
Interventional
Intervention
Afatinib
Talcum powder
Sponsored by

About this trial
This is an interventional treatment trial for Non Small Cell Lung Cancer focused on measuring Afatinib, Talcum powder, Thoracoscopy, Pleurodesis, BIBW2992
Eligibility Criteria
Inclusion Criteria:
- Non-small cell lung cancer with positive mutation of EGFR verified
- Malignant pleural effusion
- Recurrent pleural effusion
- Complete lung expansion (> 80%) after puncture emptying confirmed by chest radiography.
- Karnofsky index > 50
- Agreed to participate in the study and sign an Informed Consent
Exclusion Criteria:
- Radiotherapy not earlier than 3 months before the pleurodesis procedure
- Previous surgeries on the same hemitorace
- Thrombocytopenia or coagulation disorders
- Trapped lung syndrome
- Patients with estimated life expectancy < 4-8 weeks
- Pleural or active systemic infection
Sites / Locations
- Central Contact
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Talcum powder & Afatinib
Arm Description
Talcum powder 4 g + Afatinib 0,4 g. Is entered once
Outcomes
Primary Outcome Measures
The effectiveness of the procedure of dry pleurodesis through a thoracoscope
Evaluation of the effectiveness of the dry pleurodesis procedure in combination with talc and afatinib with the introduction of a powder suspension through a thoracoscope.
The assessment is performed by CT (computed tomography) of each participant twice: 30 days from the day of the procedure and 90 days later.
Secondary Outcome Measures
Full Information
NCT ID
NCT03827070
First Posted
January 29, 2019
Last Updated
April 23, 2023
Sponsor
Center Trials & Treatment Europe
Collaborators
Center Trials & Treatment
1. Study Identification
Unique Protocol Identification Number
NCT03827070
Brief Title
Dry Pleurodesis With Talcum and Afatinib is Used to Treat Patients With Non-Small Cell Lung Carcinoma
Acronym
DPTA
Official Title
New Method of Treatment for Thoracoscopy or Bronchoscopy by Suspension of Fine Powder of Talcum and Afatinib is Used in Patients With Positive Mutation of EGFR in Non-Small Cell Lung Carcinoma (NSCLC)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 5, 2019 (Actual)
Primary Completion Date
February 21, 2023 (Actual)
Study Completion Date
July 21, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Center Trials & Treatment Europe
Collaborators
Center Trials & Treatment
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In non-small cell lung cancer and metastases in the pleural cavity, pathological effusion is formed.
Currently, the most common and effective method of obliteration of the pleural cavity is pleurodesis with talcum powder.
Talc, when it surface of the pleura, causes chemical inflammation that leads to the soldering of the lungs and chest wall. As a result, the liquid ceases to accumulate.
The addition of a therapeutic dose of afatinib to talc not only blocks effusion into the pleural cavity, but also reduces tumor and metastatic processes.
Detailed Description
The proposed procedure for dry pleurodesis consists of one stage.
Talc is introduced into the pleural cavity in several ways:
Drainage - a tube is inserted into the pleural cavity through a puncture in the chest, and then a pasty talcum is delivered into the cavity, which spreads through the cavity during the change of the patient's body position.
Talcum powder - under the control of thoracoscopy, dry talc is blown into the pleural cavity of the patient, which allows him to evenly distribute and significantly increases the effectiveness of the procedure.
In this Clinical Trial investigators will use the method of thoracoscopy - the blow in of talcum powder and therapeutic dose of Afatinib. Before injection, a suspension of talc and afatinib is subjected to the procedure of pharmaceutical mixing.
The operation is well tolerated by participants and lasts no more than 30 minutes. The effectiveness of the method is 90%.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Small Cell Lung Cancer
Keywords
Afatinib, Talcum powder, Thoracoscopy, Pleurodesis, BIBW2992
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Single Group Assignment
Masking
None (Open Label)
Masking Description
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Talcum powder & Afatinib
Arm Type
Experimental
Arm Description
Talcum powder 4 g + Afatinib 0,4 g. Is entered once
Intervention Type
Drug
Intervention Name(s)
Afatinib
Other Intervention Name(s)
BIBW2992
Intervention Description
Used Afatinib particles of which had an average size of 22 μm and a volume concentration of small particles (<5 μm) - only 19%
Intervention Type
Drug
Intervention Name(s)
Talcum powder
Other Intervention Name(s)
Talc
Intervention Description
Used Talcum powder particles of which had an average size of 24.5 μm and a volume concentration of small particles (<5 μm) - only 11%
Primary Outcome Measure Information:
Title
The effectiveness of the procedure of dry pleurodesis through a thoracoscope
Description
Evaluation of the effectiveness of the dry pleurodesis procedure in combination with talc and afatinib with the introduction of a powder suspension through a thoracoscope.
The assessment is performed by CT (computed tomography) of each participant twice: 30 days from the day of the procedure and 90 days later.
Time Frame
up to 90 days
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Non-small cell lung cancer with positive mutation of EGFR verified
Malignant pleural effusion
Recurrent pleural effusion
Complete lung expansion (> 80%) after puncture emptying confirmed by chest radiography.
Karnofsky index > 50
Agreed to participate in the study and sign an Informed Consent
Exclusion Criteria:
Radiotherapy not earlier than 3 months before the pleurodesis procedure
Previous surgeries on the same hemitorace
Thrombocytopenia or coagulation disorders
Trapped lung syndrome
Patients with estimated life expectancy < 4-8 weeks
Pleural or active systemic infection
Facility Information:
Facility Name
Central Contact
City
Tbilisi
ZIP/Postal Code
0008
Country
Georgia
12. IPD Sharing Statement
Learn more about this trial
Dry Pleurodesis With Talcum and Afatinib is Used to Treat Patients With Non-Small Cell Lung Carcinoma
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