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Updated: Jun 29, 2025

Profiling Sensitivity to Targeted Therapies in EGFR-Mutant NSCLC Patient-Derived Organoids
Published on: November 22, 2021
Early dose reduction of osimertinib in advanced EGFR -mutated non-small cell lung cancer
Marion Ferreira1,2, Matthew I Ebia3, Karen L Reckamp3
1Department of Pneumology and Respiratory Functional Exploration, University Hospital of Tours.
Abstract:
Osimertinib has become the standard of care for epidermal growth factor receptor ( EGFR )-mutated non-small cell lung cancer (NSCLC). In order to prevent or treat toxicity, the osimertinib dose may be reduced. However, data regarding the impact of dose reduction during treatment are limited. We aimed to compare the efficacy of osimertinib early dose reduction during the first 3 months of treatment with late dose reduction in EGFR -mutated advanced NSCLC. This retrospective study included patients with EGFR -mutated advanced NSCLC who received osimertinib. We constituted two groups: 'early dose reduction' (early) with patients receiving a reduced dose of osimertinib from 80 to 40 mg within the 3 months of osimertinib initiation and 'late dose reduction' (late) with patients receiving a reduced dose after 3 months of full-dose treatment. Thirty-five patients were included, with 17 and 18 patients in the early and late groups, respectively, and a higher median age in the early group (76 vs. 67 years). The real-world progression-free survival (rwPFS) at 1 year was 70.5% in the early group and 88.9% in the late group ( P = 0.31). Median rwPFS was 32.7 and 24.6 months ( P = 0.98), and the median overall survival was 46.9 versus not reached in early and late groups, respectively ( P = 0.17). Central nervous system rwPFS was not different between the early and late groups: 29.8 and 35.8 months, respectively ( P = 0.39). We showed that a reduced dose of osimertinib within the first 3 months of treatment, compared to a later reduced dose, could influence treatment response or patient survival.
Insights
Reducing osimertinib dose early in treatment for EGFR-mutated non-small cell lung cancer may impact patient outcomes. This study compared early versus late dose reductions, finding potential differences in treatment response and survival.
Area of Science:
- Oncology
- Pharmacology
Background:
- Osimertinib is a standard treatment for EGFR-mutated non-small cell lung cancer (NSCLC).
- Dose reduction of osimertinib is sometimes necessary due to toxicity.
- Limited data exist on the impact of early versus late dose reduction on treatment efficacy.
Purpose of the Study:
- To compare the efficacy of early versus late dose reduction of osimertinib in patients with EGFR-mutated advanced NSCLC.
- To evaluate the influence of dose modification timing on real-world progression-free survival (rwPFS) and overall survival.
Main Methods:
- Retrospective study of 35 patients with EGFR-mutated advanced NSCLC treated with osimertinib.
- Patients were divided into two groups: 'early dose reduction' (within 3 months) and 'late dose reduction' (after 3 months).
- Comparison of rwPFS, overall survival, and central nervous system rwPFS between the two groups.
Main Results:
- One-year rwPFS was 70.5% in the early group and 88.9% in the late group (P=0.31).
- Median rwPFS was 32.7 months (early) vs. 24.6 months (late) (P=0.98).
- Median overall survival was 46.9 months (early) vs. not reached (late) (P=0.17).
Conclusions:
- Early dose reduction of osimertinib within the first 3 months may influence treatment response and patient survival compared to later dose reduction.
- Further research is needed to fully understand the implications of osimertinib dose modification timing.
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