# Safety and efficacy of osimertinib 160 mg daily given concurrently with a strong CYP3A4 inducer

**Authors:** Mostafa Aglan, Erin Spyropoulous, Joel Oster, Paul J. Hesketh, A.J. Piper-Vallillo

PMC · DOI: 10.1016/j.rmcr.2025.102200 · Respiratory Medicine Case Reports · 2025-04-01

## TL;DR

A patient with lung cancer safely and effectively received a higher dose of osimertinib while taking a drug that lowers its concentration in the body.

## Contribution

First reported case of safely using 160 mg osimertinib with a strong CYP3A4 inducer in EGFR-mutant NSCLC.

## Key findings

- Dose-escalated osimertinib (160 mg) with a CYP3A4 inducer provided durable disease control for over 32 months.
- The treatment was well-tolerated with minimal side effects despite the drug interaction.
- The patient achieved a partial response and stable disease while on concurrent therapy.

## Abstract

Osimertinib remains the standard first-line therapy for patients with advanced EGFR-mutant NSCLC, at least in part due to its improved CNS penetrance compared to earlier generation EGFR TKIs. Strong CYP3A4-inducing medications are known to reduce the effective concentration of osimertinib, prompting the recommendation to double the standard osimertinib dose from 80 to 160 mg daily. However, little is known about the real-world safety and efficacy of osimertinib given in combination with long term CYP3A4 inducer use. We detail, to our knowledge, the first reported case of a patient receiving an escalated osimertinib dosage concurrent with a potent CYP3A4 inducer.

A 69-year-old-female with a long-standing history of a seizure disorder was diagnosed with stage IV EGFR exon 19 deletion positive lung adenocarcinoma. After a failed trial to wean the patient off phenytoin, osimertinib at a dose of 160 mg in combination with phenytoin was recommended based on existing clinical guidelines. She achieved a partial response and continues with stable disease for more than 32 months from initiation of osimertinib. Additionally, she tolerated osimertinib well with minimal side effects although with persistent dyspnea of unclear etiology.

Our case illustrates that 160 mg of osimertinib administered concurrently with a strong CYP3A4 inducer can be given safely and with retained efficacy in treating CNS metastatic EGFR-positive non-small cell lung cancer.

•Patient with advanced EGFR Ex19del+ NSCLC required concurrent treated with osimertinib and a strong CYP3A4 inducer.•Dose-escalated osimertinib (160 mg daily) co-administered with a CYP3A4 inducer provided durable disease control.•Concurrent dosing was well-tolerated, with minimal side effects, supporting the feasibility of this dosing approach.

Patient with advanced EGFR Ex19del+ NSCLC required concurrent treated with osimertinib and a strong CYP3A4 inducer.

Dose-escalated osimertinib (160 mg daily) co-administered with a CYP3A4 inducer provided durable disease control.

Concurrent dosing was well-tolerated, with minimal side effects, supporting the feasibility of this dosing approach.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Chemicals:** osimertinib (PubChem CID 71496458), phenytoin (PubChem CID 1775)
- **Diseases:** NSCLC (MONDO:0005233), lung adenocarcinoma (MONDO:0005061)

## Full-text entities

- **Genes:** CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** dyspnea (MESH:D004417), lung adenocarcinoma (MESH:D000077192), non-small cell lung cancer (MESH:D002289), seizure disorder (MESH:D004827)
- **Chemicals:** phenytoin (MESH:D010672), Osimertinib (MESH:C000596361)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12008127/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12008127/full.md

## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12008127/full.md

---
Source: https://tomesphere.com/paper/PMC12008127