Study of Osimertinib+Bevacizumab+Chemotherapy for EGFR+ Advanced Non-Small Cell Lung Cancer With Concurrent Mutations
- Sponsor
- Tianjin Medical University Cancer Institute and Hospital
- Study ID
- NCT05507606
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Osimertinib — DRUGosimertinib 80mg/d
- Bevacizumab Biosimilar IBI305 — DRUGBevacizumab, 7.5mg/kg d1; was discontinued after 2 years
- Carboplatin — DRUGCarboplatin AUC5, d1; was stopped after 4 cycles
- Pemetrexed — DRUGPemetrexed, 500mg/m2, d1;Q3W/cycle; was discontinued after 2 years
Study Details
This is a single-center, open-label, phase I clinical trial aimed to evaluate the efficacy and safety of Osimertinib+Bevacizumab+Carboplatin and Pemetrexed for Untreated Patients With EGFR Mutation Advanced Non-squamous Non-Small Cell Lung Cancer With Concomitant Mutations.
Key Dates
- Start date
- Aug 1, 2021
- Status verified
- Aug 2022
- Primary completion
- Aug 1, 2023
- Completion
- Aug 1, 2024
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Osimertinib+Bevacizumab+Carboplatin and PemetrexedBevacizumab, 7.5mg/kg, d1; Pemetrexed, 500mg/m2, d1; Carboplatin AUC5, d1; Osimertinib 80mg/d , d1-21; Q3W/cycle induction therapy for 4 cycle. Then Carboplatin was stopped after 4 cycles, and Osimertinib combined with Bevacizumab and Pemetrexed were given for maintenance treatment every 3 weeks for 2 years. After that, the maintenance treatment of Osimertinib was continued.
Primary Outcome Measure
ORR [ Time Frame: 2 years ]
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