None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Male or female subjects 20 years of age or older at the time of diagnosis 2) Patients with histologically or cytologically proven diagnosis of EGFR T790M positive NSCLC 3) Patients who were treated with Osimertinib between Jan 1st, 2018 and June 30th, 2020
Exclusion criteria
Exclusion criteria: 1) Patients who received osimertinib in clinical trial setting 2) Patients whose medical records are not available for review
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression-free survival (PFS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Treatment profiles of Osimertinib; Duration of response (DoR); Disease control rate (DCR) at 6 and 12 weeks;Time to overall progression [TTP], time to intracranial progression [IC-TTP], time to extracranial progression [EC-TTP];Overall survival (OS) | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center