Management of Advanced Non-Small Cell Lung Cancer (NSCLC) and Clinical Outcomes in Patients Who Received Gefitinib in Thailand
Completed
- Conditions
- Lung Cancer
- Registration Number
- NCT01130961
- Lead Sponsor
- AstraZeneca
- Brief Summary
The purpose of this study is to determine progression-free survival of lung cancer patients who received gefitinib in clinical practice in Thailand.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 104
Inclusion Criteria
- Diagnosed as having lung cancer based on histological/cytological findings
- Admitted to the hospital between January 2004 and December 2008
- Treated with gefitinib for at least 3 months
Exclusion Criteria
- Involvement in the planning and/or conduct of the study
- Participation in another clinical study during the last 3 months
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Progression-free survival median time from the first date of treatment until date of disease progression during Jan 2004- Dec 2008 or 5 years approx.
- Secondary Outcome Measures
Name Time Method Prevalence of EGFR & KRAS mutation from laboratory result During Jan 2004- Dec 2008 or 5 years approx. Time to maximum response Median time from the first date of treatment until the date that the disease can be maximum controlled during Jan 2004- Dec 2008 or 5 years approx. Overall survival time from the first date of treatment until date of patients dead during Jan 2004- Dec 2008 or 5 years approx.
Trial Locations
- Locations (1)
Research Site
🇹🇭Bangkok, Thailand