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Clinical Trial Summary

To evaluate the efficacy and safety of SBRT for T1N0M0 non-small cell lung cancer


Clinical Trial Description

To evaluate the efficacy and safety of SBRT for T1N0M0 non-small cell lung cancer,the following questions should be answered. Can SRT be an alternative standard treatment modality for inoperable patients? Can SRT can be a comparable standard treatment modality with lobectomy for operable patients? 12 Gy is the daily dose at the isocenter,and 48 Gy in total by 4 fractions will be irradiated by stereotactic irradiation over 4 to 8 days. ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00238875
Study type Interventional
Source Japan Clinical Oncology Group
Contact
Status Completed
Phase Phase 2
Start date July 2004
Completion date November 2011