Treatment Strategies and Survival Outcome for Non-small Cell Lung Cancer With Oncogenic Mutation
- Sponsor
- Hunan Province Tumor Hospital
- Study ID
- NCT04322890
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- ALK Gene Mutation
- EGFR Gene Mutation
- MET Gene Mutation
- Non Small Cell Lung Cancer
- ROS1 Gene Mutation
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Osimertinib — DRUGOsimertinib 80mg, po, qd;
- Alectinib 150 MG — DRUGAlectinib 600mg, po, qd; Lorlatinib, 100mg, po, qd;
- Crizotinib 250 MG — DRUGCrizotinib 250 MG po bid.
- Savolitinib, Crizotinib. — DRUGSavolitinib, 300mg po qd.
- Chemotherapy — DRUG500mg, ivgtt, every 21day.
Study Details
The purpose of this study is to assess the Treatment Strategies and Survival Outcome for Non-small Cell Lung Cancer With Oncogenic Mutation.
Key Dates
- Start date
- Apr 16, 2020
- Status verified
- Oct 2024
- Primary completion
- Dec 24, 2026
- Completion
- Dec 24, 2027
Study Design
- Enrollment
- 6,000 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort A: EGFR mutationLung Cancer with EGFR mutation including EGFR exon19del, exon 21L858R, etc.
- Experimental: Cohort B: ALK fusionLung Cancer with ALK fusion.
- Experimental: Cohort C: ROS1 fusionLung Cancer with ROS1 fusion.
- Experimental: Cohort D: MET alterationsLung Cancer with MET alteration including amplification, exon 14 skipping and met fusion etc.
- Experimental: Cohort E: RET fusionLung Cancer with RET fusion.
- Experimental: Cohort F: KRAS mutationLung Cancer with KRAS mutation.
- Experimental: Cohort G: uncommon mutationCohort G mainly includes all identified lung cancer mutations except EGFR mut, ALK fusion, ROS1 fusion, MET alterations, KRAS mut and RET fusion. These include: BRAF V600E and non-V600E, NRG fusion, NTRK fusion, ERBB2 amp and mut,NRAS mut, MAP2K1 mut,RIT1 mut, RAF1 mut, FGFR fusion, ARAF mut, HRAS mut etc.
Primary Outcome Measure
Progression-free survival (PFS) [ Time Frame: Time from first subject dose to study completion, or up to 36 month ]
Central Contacts
- Yongchang Zhang, MD+8613873123436
- Nong Yang, MD+8613055193557
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