This is a local, prospective, non-interventional, regulatory postmarketing surveillance study. The objectives of this study are to assess the safety and efficacy of single agent Tagrisso (Osimertinib, hereinafter "the study drug") in a real world setting according to the approved label in Korea.
* Primary objective: To assess safety of the Tagrisso for patients with NSCLC treated with Tagrisso under the approved indication in Korea * Secondary objective: To assess efficacy of the Tagrisso for patients with NSCLC treated with Tagrisso under the approved indication in Korea.
Study Type
OBSERVATIONAL
Enrollment
923
Research Site
Busan, South Korea
Research Site
Chungcheongbuk-do, South Korea
Research Site
Daegu, South Korea
Research Site
Daejeon, South Korea
Proportion (%) of patients with at least one event of adverse events (AEs), serious adverse events (SAEs) and AEs of special interest (AESI)
Time frame: For about 1 year since the first dose of the study drug
Severity of (S)AEs according to CTCAE
Time frame: For about 1 year since the first dose of the study drug
ORR (Objective response rate), if available
Time frame: For about 1 year since the first dose of the study drug
PFS (Progression free survival) , if available
Time frame: For about 1 year since the first dose of the study drug
DFS (Disease free survival), if available
Time frame: For about 1 year since the first dose of the study drug
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Research Site
Gangwon State, South Korea
Research Site
Gyeonggi-do, South Korea
Research Site
Incheon, South Korea
Research Site
Jeollabuk-do, South Korea
Research Site
Jeollanam-do, South Korea
Research Site
Seoul, South Korea