Lung Cancer Clinical Trial
Official title:
A Pilot Study of Radiofrequency Ablation in High-Risk Patients With Stage IA Non-Small Cell Lung Cancer
This pilot clinical trial studies how well radiofrequency ablation works in treating patients with stage IA non-small cell lung cancer. Radiofrequency ablation uses high-frequency electric current to kill tumor cells. Computed tomography (CT)-guided radiofrequency ablation may be a better treatment for non-small cell lung cancer.
PRIMARY OBJECTIVES:
I. To assess the overall 2-year survival rate after radiofrequency ablation (RFA).
SECONDARY OBJECTIVES:
I. To assess freedom from regional or distant recurrence. II. To assess freedom from local
recurrence in the ablated lobe. III. To estimate the number of procedures deemed technical
successes. IV. To evaluate procedure-specific morbidity and mortality. V. To explore the
utility of immediate (within 96 hours) post-RFA positron emission tomography (PET) in
predicting overall survival and local control.
VI. To explore the effect of RFA on both short-term (3 months post-RFA) and long-term (24
months post-RFA) pulmonary function.
OUTLINE:
A radiofrequency electrode is placed by CT guidance into the target tumor. Patients undergo
RFA directly to the tumor for up to 12 minutes to obtain an intratumoral temperature > 60°
Celsius (C). Patients may receive 3 RFA treatments (a total of 36 minutes) to obtain the
target temperature.
After completion of study treatment, patients are followed every 3 months for 1 year and
then every 6 months for 1 year.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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