Neoadjuvant Targeted Therapy in Patients With Resectable EGFR-mutated Lung Squamous Cell Carcinoma
- Sponsor
- The First Affiliated Hospital of Guangzhou Medical University
- Study ID
- NCT06383728
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Carcinoma, Squamous Cell
- Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Osimertinib — DRUGPatients with resectable stage II-IIIB EGFR-mutated lung squamous cell carcinoma will receive Osimertinib ( 80mg/d, ≥9 weeks).
Study Details
Previous trials, such as ADURA and CTONG, have demonstrated the benefits of neoadjuvant targeted therapy in patient with EGFR mutations , which can effectively reduce the extent of tumors and improve the survival outcomes. However, clinical trials of neoadjuvant targeted therapy in NSCLC have rarely enrolled patients with EGFR-mutated lung squamous cell carcinoma due to its rarity, which means that the safety and feasibility of neoadjuvant osimertinib in patients with resectable stage II-IIIB EGFR-mutated lung squamous cell carcinoma remains controversial.
Key Dates
- Start date
- Apr 1, 2024
- Status verified
- May 2024
- Primary completion
- Oct 31, 2025
- Completion
- Apr 30, 2029
Study Design
- Enrollment
- 51 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: OsimertinibPatients with resectable stage II-IIIB EGFR-mutated lung squamous cell carcinoma will receive Osimertinib ( 80mg/d, ≥9 weeks).
Primary Outcome Measure
Objective Response Rate, ORR [ Time Frame: analysis is completed 4 weeks after neoadjuvant treatment ]
Central Contacts
- Shuben Li, Doctor13500030280
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