Neoadjuvant Furmonertinib Plus Bevacizumab or Furmonertinib Monotherapy for Resectable and Potentially Resectable Stage III-IVA EGFR Mutation-Positive Lung Adenocarcinoma
Neoadjuvant Furmonertinib Plus Bevacizumab or Furmonertinib Monotherapy for Resectable and Potentially Resectable Stage III-IVA EGFR Mutation-Positive Lung Adenocarcinoma: A Randomized, Controlled, Open-label, Single-center Phase II Clinical Trial
Shanghai Pulmonary Hospital, Shanghai, China
96 participants
Feb 1, 2022
INTERVENTIONAL
Conditions
Summary
To explore the efficacy and safety of neoadjuvant furmonertinib combined with bevacizumab in the treatment of resectable and potentially resectable stage III-IVA EGFR mutation-positive lung adenocarcinoma.
Eligibility
Plain Language Summary
Simplified for easier understanding
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Interventions
Furmonertinib 80 mg/day for 16 weeks
bevacizumab 400 mg/4 weeks i.v. for 4 times
Locations(1)
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NCT05503667