Evaluation of the Efficacy and Safety of Furmonertinib Combined with Bevacizumab As First-Line Treatment for EGFR-Positive Non-Small Cell Lung Cancer with Brain Metastases: a Single-Arm, Open-Label, Prospective Phase II Clinical Study

This study evaluates the safety and efficacy of Befotertinib combined with Bevacizumab as a first-line treatment for patients with EGFR mutation-positive advanced non-small cell lung cancer (NSCLC) accompanied by brain or leptomeningeal metastases. It is a single-arm, open-label, prospective Phase II clinical trial aiming to explore the potential benefits of this combination therapy in improving intracranial progression-free survival (iPFS) and overall survival (OS). Patients will receive Befotertinib daily and Bevacizumab every three weeks until disease progression, intolerable toxicity, or w

Trial Details

NCT ID
NCT06728865
Phase
PHASE2
Sponsor
Li-kun Chen
Status
RECRUITING
Cancer Type
Brain Cancer
Interventions
  • The treatment regimen is Furmonertinib combined with Bevacizumab.
Locations (sample)
  • Guangzhou, Guangdong, China|23.11667,113.25

Key Eligibility Criteria

  • Aged 18-75 years. ECOG performance status (PS) score of 0-2. Expected survival time of ≥3 months.
  • Histologically or cytologically confirmed non-squamous non-small cell lung cancer (NSCLC).
  • Baseline evaluation confirming the presence of EGFR-sensitizing mutations (19del/L858R) via first- or second-generation sequencing. Test samples ca…
  • Asymptomatic brain metastases or those with controlled intracranial hypertension symptoms following dehydration treatment. Continued medication to …

For full eligibility, visit ClinicalTrials.gov.

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