A phase II study is conducted to determine the efficacy and safety of a single agent Camtobell inj.(belotecan) on a weekly schedule in locally advanced or metastatic non-small cell lung cancer patients previously treated with chemotherapy. The usefulness of the this regimen is evaluated by response rate, median survival time, progression free survival and duration of response.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
52
3.0 mg/m2, Day 1, 8, 15 every 4 weeks
Objective Response Rate
Time frame: every 2 cyc
Overall Survival
Time frame: 6 months after Last patient out
Progression Free survival
Time frame: 6 months after Last patient out
Adverse event
Time frame: every visit
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