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Dry Pleurodesis With Talcum and Afatinib is Used to Treat Patients With Non-Small Cell Lung Carcinoma (DPTA)

C

Center Trials & Treatment Europe

Status and phase

Active, not recruiting
Phase 1

Conditions

Non Small Cell Lung Cancer

Treatments

Drug: Afatinib
Drug: Talcum powder

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT03827070
9TJJ425H1D

Details and patient eligibility

About

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.

Full 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%.

Enrollment

12 patients

Sex

Male

Ages

21 to 40 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

Talcum powder & Afatinib
Experimental group
Description:
Talcum powder 4 g + Afatinib 0,4 g. Is entered once
Treatment:
Drug: Afatinib
Drug: Talcum powder

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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