None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Retrospective cohort: patients who have completed afatinib treatment between September 2018 and the day before the starting day of this study. Prospective cohort: patients who are treated with afatinib without disease progression at study initiation, or patients who are to initiate afatinib after study initiation. 1) Patients who recieved afatinib in locally advanced, metastatic or recurrent squamous cell carcinoma of lung progressed after platinum-based chemotherpay with/without immunotherapy from September 2018 to November 2021. 2) Patients who provide written informed consent for the study (But, obtaining informed consent will be exempted for patients in a retrospective cohort or expired patients)
Exclusion criteria
Exclusion criteria: 1) Patients who were treated with other EGFR-TKIs 2) Illiterate 3) Women of pregnant or childbearing potential who are planning on becoming pregnant 4) patinets under the age of 19
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to treatment failure (TTF) | — |
Secondary
| Measure | Time frame |
|---|---|
| Objective response rate (ORR);Progression-free survival (PFS);Overall survival (OS);Disease control rate (DCR);Duration of Response (DR);Differences in TTF, PFS, and OS according to genetic alterations and PD-L1 expression status;Safety profile | — |
Countries
Korea, Republic of
Contacts
Kyung Hee University Hospital