Lung Cancer Clinical Trial
Official title:
A Phase II Trial of Stereotactic Body Radiation Therapy (SBRT) in the Treatment of Patients With Operable Stage I/II Non-Small Cell Lung Cancer
RATIONALE: Stereotactic body radiation therapy may be able to send x-rays directly to the
tumor and cause less damage to normal tissue near the tumor.
PURPOSE: This phase II trial is studying how well stereotactic body radiation therapy works
in treating patients with stage I or stage II non-small cell lung cancer that can be removed
by surgery.
OBJECTIVES:
Primary
- Determine whether treatment with radiotherapy involving a high biological dose with
limited treatment volume (using stereotactic body radiotherapy [SBRT] techniques)
achieves acceptable primary tumor control (i.e., ≥ 90% at 2 years) in patients with
resectable early-stage non-small cell lung cancer.
Secondary
- Determine whether treatment with radiotherapy involving a high biological dose with
limited treatment volume (using SBRT techniques) achieves acceptable treatment-related
toxicity.
- Estimate the disease-free survival and the overall survival rate at 2 years.
- Observe patterns of failure in the first 2 years.
- Assess the level of comorbidity burden on morbidity and efficacy.
- Determine if blood markers prior to, during the course of treatment (between the second
and the last dose of SBRT), and at the first follow-up after SBRT predict 2-year primary
tumor control and predict for grade ≥ 2 treatment-related toxicities
OUTLINE: This is a multicenter study.
Patients receive 3 fractions of stereotactic body radiotherapy over 14 days. Patients with
disease progression undergo surgical resection as salvage local therapy.
After completion of study therapy, patients are followed every 3 months for 2 years, every 6
months for 3 years and then annually thereafter.
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