Abstract
PURPOSE: EGFR-mutated (EGFRm) NSCLC is associated with high incidence of brain metastases and leptomeningeal disease (LMD), for which effective systemic options beyond osimertinib 80 and 160 mg daily are limited. While there is some evidence for high-dose pulse administration of earlier-generation EGFR tyrosine kinase inhibitors (EGFK-TKIs), data for pulse-dose osimertinib are limited. METHODS: This multicenter retrospective case series included patients with EGFRm NSCLC with LMD or parenchymal brain metastases treated with pulse-dose osimertinib (400-560 mg once every 5-7 days) for central nervous system (CNS) progression, with or without other concurrent therapies. CNS disease control was defined as the interval from pulse-dose osimertinib initiation to radiographic progression or discontinuation for clinical progression, whichever was shorter. RESULTS: Among 14 patients, EGFR mutations included exon 19 deletion in 6, L858R in 6, and other mutations in 4. All had received previous EGFR-TKI including 5 with prior osimertinib 160 mg daily. Seven received pulse-dose osimertinib as monotherapy, while the remainder received it in combination with other systemic therapy and/or CNS radiation. No treatment-related severe or unexpected side effects were reported, and only 1 patient required dose modification for adverse events. Median duration of CNS control was 4.0 months (95% CI, 1.8-NR) and median overall survival was 6.2 months (95% CI, 3.2-NR), with benefit driven by patients without previous osimertinib 160 mg daily exposure. CONCLUSION: Though further pharmacokinetic investigation is warranted, this report provides preliminary evidence that pulse-dose osimertinib may be a safe regimen among patients with EGFRm NSCLC and refractory CNS disease.