A Pan-Asian Clinical Database of EGFR Exon 20 Insertion Mutated NSCLC
NCT06418412
Summary
There are limited in depth studies on the epidemiology and clinical management of EGFR exon 20 insertion mutated NSCLC in Asia. In addition, there is preliminary data suggesting the exact location of the insertion and variant may influence the response and efficacy to novel EGFR targeted therapies. This study aims to fill this knowledge gap, by comprehensively characterising the epidemiology and clinical outcomes of Asian advanced EGFR exon 20 insertion mutated NSCLC patients.
Eligibility
Inclusion Criteria: 1. Histologically confirmed advanced NSCLC 2. Positive testing result from any locally approved test (including but not limited to RT-PCR, Cobas and NGS) for EGFR exon 20 insertion mutation 3. Diagnosis date from 1 Jan 2013 to 31 Dec 2024 (to allow for minimum 12 months of follow-up clinical and treatment outcome data) 4. Male or female adults, age as defined by local regulations Exclusion Criteria: 1\. Patients without an EGFR exon 20 insertion mutation
Conditions3
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NCT06418412