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Combining Osimertinib With Chemotherapy in EGFR-Mutant NSCLC at Progression
Maya N White1, Zofia Piotrowska2, Kevin Stirling3
1Department of Medicine, Division of Oncology, Stanford University, Stanford, CA.
Combining osimertinib with chemotherapy in advanced non-small cell lung cancer (NSCLC) showed promising central nervous system (CNS) control and manageable safety. This combination therapy demonstrated favorable duration on treatment and overall survival in heavily pre-treated patients.
Area of Science:
- Oncology
- Pharmacology
- Medical Research
Background:
- Osimertinib, a third-generation EGFR tyrosine kinase inhibitor, has shown efficacy in non-small cell lung cancer (NSCLC) with EGFR mutations.
- Limited data exists on the combination of osimertinib with chemotherapy in advanced NSCLC.
- Understanding the efficacy and safety of this combination is crucial for treatment optimization.
Purpose of the Study:
- To evaluate the efficacy and safety of combining osimertinib with chemotherapy in advanced EGFR-mutated NSCLC.
- To assess outcomes including duration on treatment (DOT), overall survival (OS), and central nervous system (CNS) control.
- To analyze safety profiles of concurrent osimertinib and chemotherapy regimens.
Main Methods:
- Retrospective study at three institutions involving patients with advanced EGFR-mutated NSCLC.
- Inclusion criteria: concurrent osimertinib and chemotherapy in the third-line or beyond.
- Data collection via chart review, assessing efficacy (DOT, OS, CNS outcomes) and safety.
Main Results:
- 44 patients met inclusion criteria; 28 received osimertinib plus platinum doublet, 29 received osimertinib plus single-agent chemotherapy.
- Median DOT was 6.1 months with platinum doublet and 2.6 months with single-agent chemotherapy.
- Median OS was 10.4 months; 84% had CNS metastases at baseline, with 24% experiencing CNS progression.
Conclusions:
- Combination of osimertinib plus chemotherapy appears safe in advanced NSCLC patients with prior treatment progression.
- Favorable CNS disease control was observed in this cohort.
- DOT and survival outcomes were comparable to historical chemotherapy controls.
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