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SHO Mitsuya
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P76 - Targeted Therapy - Clinically Focused - EGFR (ID 253)
- Event: WCLC 2020
- Type: Posters
- Track: Targeted Therapy - Clinically Focused
- Presentations: 1
- Moderators:
- Coordinates: 1/28/2021, 00:00 - 00:00, ePoster Hall
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P76.23 - A Retrospective Study of Non-Small Cell Lung Cancer Treated with Second- and Third-Generation EGFR Tyrosine Kinase Inhibitors (ID 1347)
00:00 - 00:00 | Presenting Author(s): SHO Mitsuya
- Abstract
Introduction
Various clinical trials have evaluated first- to third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) as the first-line treatment for EGFR-mutated non-small cell lung cancer (NSCLC). Although recent research evidence supports the use of third-generation TKIs such as osimertinib as therapeutic agents for patients with EGFR-mutated NSCLC, there are no reports of clinical trials comparing second-generation such as afatinib and third-generation TKIs. Further prospective evaluation is required.
Methods
Clinical research data from the Osaka Medical College Hospital were retrospectively analyzed. All patients diagnosed with EGFR-mutated NSCLC who were treated with afatinib or osimertinib as first-line treatment from January 2015 to December 2019 were included. Systemic progression-free survival (PFS) and overall survival (OS) were evaluated.
Results
A total of 47 patients were included in this study. Of these, 13 patients received afatinib and 34 osimertinib. Patients on afatinib treatment had a median age of 68; 7 were male and 6 were female. Patients on osimertinib treatment had a median age of 72; 14 were male and 20 were female. The performance status (0/1/≧2) of afatinib and osimertinib was 4/9/0 and 6/25/3, respectively. The type of EGFR mutation (Exon 19 deletion/L858R/Others) differed between afatinib (6/4/3) and osimertinib (14/17/3). Progression-free survival analysis indicated no significant differences between the two groups: afatinib 18 months vs. osimertinib, which could not be calculated (hazard ratio = 0.576; 95% confidence interval = 0.171-1.941; P=0.356). Overall survival in months was calculated: afatinib could not be calculated vs. 33 months for osimertinib (hazard ratio = 1.981; 95% confidence interval = 0.348-11.273; P=0.422). Afatinib was superior to osimertinib in the objective response rate (afatinib, 76.9% vs. osimertinib, 64.7%). Severe adverse events (grade≧3) were more reported for afatinib than for osimertinib (23.1% vs. 14.7%).
Conclusion
Second- and third-generation TKIs are both appropriate first-line treatments for EGFR-mutated NSCLC.