Condition: Non Small Cell Lung Cancer · EGFR Exon 20 Insertion Mutation · Sponsor: Juan LI, MD
This is a phase II, prospective, multi-centre study. To assess the efficacy and safety of furmonertinib in patients with epidermal growth factor receptor 20ins mutation positive stage IB-IIIA Non-small Cell Lung Carcinoma, following complete tumour resection with or without adjuvant chemotherapy. The study plans to enroll 20 subjects, treating with furmonertinib 160mg/d, until disease recurrence, death or intolerability. The maximum duration of treatment is three years. The primary endpoint is DFS. The secondary endpoint include DFS rate , OS and the change of HRQoL. In addition, the peripheral blood ctDNA will be collected and analyzed in this study
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| Sichuan cancer hospital | Chengdu, Sichuan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06192849