Feasibility Study of the RF Ablation Catheter to Ablate Lung Tumors

Broncus Medical

Status

Terminated

Conditions

Lung Cancer Metastatic

Lung Cancer

Lung Cancer, Non-small Cell

Treatments

Device: Radio-frequency Ablation

Study type

Interventional

Funder types

Industry

Identifiers

NCT03272971

Protocol 45

Details and patient eligibility

About

The feasibility of a RF ablation catheter to bronchoscopically ablate lung tumors, will be evaluated in patients already scheduled for surgical resection.

Full description

This study is a prospective, single-arm, single-center, pilot study of bronchoscopic Radio-Frequency Ablation (RFA) treatment of target lung lesions, prior to surgical tumor resection. Up to ten (10) subjects will be treated at the investigational site.

Subjects identified for this study will be those that have a surgical resection already scheduled as part of their lung cancer treatment. Patients who have consented to participate in this study (enrolled) will undergo screening assessments to evaluate the inclusion criteria associated with their lung cancer and general health. Only patients that meet all of the inclusion criteria and none of the exclusion criteria will be scheduled for RFA treatment.

Prior to RFA, high-resolution computed tomography (HRCT) scans will be used to characterize the lesion and determine the access pathways for ablation. At the time of the RFA procedure, a point-of-entry, along a bronchial wall, is created under an image-guided navigation system. The RFA catheter is advanced down the access path until it reaches the tumor and RF is administered at the prescribed dose. Upon completion of the RFA treatment, the subject is immediately prepared for surgical resection in accordance with their lung cancer standard of care. There are no follow-up visits as part of this study, the subject is excited following surgical resection.

The resected tissue will undergo pathological evaluation for tissue viability.

Enrollment

3 patients

Sex

All

Ages

21 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Proven NSCLC or pulmonary metastases from extra-thoracic primary tumor
Must be eligible for curative lung resection (lobectomy)
Tumor/lesion size will be a minimum of 10mm along the minor diameter
Willing to participate in all aspects of study protocol for duration of the study
Able to understand study requirements
Signs informed consent form

Exclusion criteria

Any contraindication to bronchoscopy, for example:
- Untreatable life-threatening arrhythmias.
- Inability to adequately oxygenate the patient during the procedure.
- Acute respiratory failure with hypercapnia (unless the patient is intubated and ventilated).
- Recent myocardial infarction.
- Previously diagnosed high-grade tracheal obstruction.
- Uncorrectable coagulopathy
Known coagulopathy
Platelet dysfunction or platelet count <100 x 10^3 cells/mm3
History of major bleeding with bronchoscopy
Suspected pulmonary hypertension: additional testing required, such as ECG
Moderate-to-severe pulmonary fibrosis
Severe emphysema (GOLD III/IV) or chronic obstructive pulmonary disease (COPD):

additional testing and PI consent is required

Bullae >5cm located within the same lobe of target tumor/lesion
Any other severe or life-threatening comorbidity that could increase the risk associated with bronchoscopic RFA
Ongoing systemic infection
Contraindications to general anesthesia
Inability to stop anticoagulants or antiplatelet agents prior to procedure as dictated by the protocol
Prior thoracic surgery on the same side of the lung as the targeted tumor/lesion
Breastfeeding women or females of childbearing potential with a positive pregnancy test prior to the procedure or the intent to become pregnant during the study
Life expectancy of less than one year.