Osimertinib and Etoposide as First-Line Treatment in Osimertinib-Resistant Advanced EGFR-Mutant NSCLC
- Sponsor
- Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
- Study ID
- NCT06436144
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
- EGFR Gene Mutation
- Non Small Cell Lung Cancer
- Non Small Cell Lung Cancer Stage IIIB
- Non-small Cell Lung Cancer Stage IV
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Osimertinib — DRUGEtoposide Soft Capsules Dosage:25mg/tablet, 2 tablets/time, taken continuously for 21 days, and stopped for one week. Osimertinib Dosage:80mg/tablet, 1 tablet/time, QD, taken for two cycles.
Study Details
Osimertinib, though a standard first-line treatment for EGFR-mutant advanced NSCLC, shows primary resistance in 10-30% of patients, leading to disease progression within 3-4 months. This resistance is linked to co-mutations in genes like TP53, RB1, and PIK3CA, among others. Studies indicate that Topo II inhibitor Etoposide (VP-16) can reduce cell survival, enhance DNA damage, and delay resistance in Osimertinib-resistant cells, suggesting a potential combination therapy to manage resistance.This study is a single-center, prospective, single-arm study evaluating the efficacy and safety of osimertinib combined with etoposide as a first-line treatment in patients with osimertinib-resistant or -insensitive advanced non-small cell lung cancer (NSCLC). The study focuses on patients with advanced NSCLC (stage IIIB or IV) with EGFR-sensitive mutations who developed slow resistance to osimertinib and for whom secondary biopsy after resistance did not identify any therapeutic targets.
Key Dates
- Start date
- Jun 30, 2024
- Status verified
- May 2024
- Primary completion
- Jun 30, 2029
- Completion
- Dec 31, 2029
Study Design
- Enrollment
- 93 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Osimertinib Combined With Etoposide Soft Capsule
Primary Outcome Measure
Objective Remission Rate (ORR) as assessed by RECIST v1.1 [ Time Frame: Within 1 month after treatment ]
Central Contacts
- He Yong86-23-68757791
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