Preoperative Percutaneous Radiofrequency Ablation of Primary and Secondary Lung Tumors

University Hospital Tuebingen

Status and phase: Completed; Phase 2

Conditions: Lung Cancer; Lung Metastasis

Treatments: Procedure: pulmonary radiofrequency ablation

Study type: Interventional

Funder types: Other

Identifiers

NCT00610844

LungRFA_V1

Details and patient eligibility

About

The purpose of the study is to evaluate the effectiveness of radiofrequency ablation by pathological correlation and to characterize the tissue response after treatment of primary and secondary pulmonary tumors.

Full description

Thermal ablation therapy is an increasingly performed technique in the local tumor treatment. Among these techniques, image-guided radiofrequency (RF) ablation attained widespread consideration in the therapy of liver tumors and osteoid osteoma. Promising results of hepatic RF ablation raised expectations to utilize the advantages of image-guided ablation therapy for the treatment of pulmonary malignancies. The purpose of the study is to evaluate the effectiveness of radiofrequency ablation by pathological correlation and to characterize the tissue response after treatment of primary and secondary pulmonary tumors. Computed tomography-guided RF ablation is performed in local or general anesthesia, followed by surgical resection three days later. An analysis of complete RF ablation and a characterization of tissue response is performed by hematoxylin and eosin staining, immunostaining, and electron microscopy. Adverse effects and complications are recorded.

Enrollment: 9 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Signed informed consent for radiofrequency ablation and surgery
• Maximum of 3 lung tumors
• Maximum tumor size 5 cm
• Must be able to receive standard surgery

Exclusion criteria

• Pathological coagulation tests
• Pregnant or breast feeding
• Maximum tumor size more than 5 cm
• Bilateral secondary lung cancer with more than 3 tumors
• Inoperable patient

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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9 participants in 1 patient group

1

Experimental group

Description:

pulmonary radiofrequency ablation

Treatment:

Procedure: pulmonary radiofrequency ablation