Neoadjuvant Furmonertinib Plus Bevacizumab or Furmonertinib Monotherapy for Resectable and Potentially Resectable Stage III-IVA EGFR Mutation-Positive Lung Adenocarcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorShanghai Pulmonary Hospital, Shanghai, China

About this trial

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 criteria

Qualifiers

Lung adenocarcinoma patient with EGFR sensitive mutation as confirmed by needle biopsy;

At stage III-IVA (TNM Staging, Version 8) as identified by chest CT, PET-CT or/and EBUS;

No systemic metastasis (confirmed by head MRI, whole body bone scan, PET-CT, liver and adrenal CT, etc.);

With the feasiblility or potential feasibility to receive radical surgery (radical lung lobectomy+systematic lymph node dissection);

Disqualifiers

The patient has undergone any systemic anti-cancer treatment for NSCLC, including cytotoxic drug treatment, targeted drug treatment and experimental treatment, etc.;

The patient suffers from any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina pectoris, angina pectoris that starts to attack within the last 3 months, congestive heart failure [≥ Grade II specified by New York Heart Association (NYHA)], cardiac infarction (6 months before enrollment), severe arrhythmia and liver, kidney or metabolic diseases that requires drug treatment;

The patient is a carrier of HIV;

The patient is currently suffering from interstitial lung disease;

Trial design

Treatments tested in this trial

  • Furmonertinib
  • Bevacizumab

Treatment groups

96 Participants
are divided into 2 treatment groups