Efficacy and Safety of Furmonertinib for Epidermal Growth Factor Receptor (EGFR) Sensitive Mutation Positive Non-Small Cell Lung Cancer (NSCLC) Patients With Brain Metastasis: a Prospective Observational Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

EGFR mutation positive advanced NSCLC patients with CNS metastases were associated with poor prognosis. Furmonertinib showed promising CNS efficacy in doses of 80 mg orally once daily or higher in patients with EGFR T790M mutation positive NSCLC. This study aims to investigate the efficacy and safety of furmonertinib in the treatment of EGFR-sensitive mutation positive NSCLC patients with brain metastasis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• at least 18 years of age;

• Histologically or cytologically confirmed metastatic non-squamous Non-Small Cell Lung Cancer (NSCLC);

• Patient with EGFR 19Del or L858R mutation diagnosed histologically or cytologically.( EGFR L858R or Del 19 with/without T790M )

• Imaging (MR/CT) confirmed untreated brain metastases before Furmonertinib initiation;

• Organ function is compatible with oral Furmonertinib therapy (investigator determination based on real-world practice);

• Life expectancy ≥12 weeks before Fumonertinib initiation;

• ECOG PS of 0 to 2;

• Sign the informed consent form.

Locations
Other Locations
China
Tangdu Hopspital
RECRUITING
Xi’an
Contact Information
Primary
Haichuan Su, PhD
such@fmmu.edu.cn
18629190366
Backup
Jie Min, PhD
minjie1504@163.com
13709202616
Time Frame
Start Date: 2022-01-28
Estimated Completion Date: 2024-09-30
Participants
Target number of participants: 30
Treatments
Furmonertinib group
Patients treated with Furmonertinib
Sponsors
Leads: Tang-Du Hospital

This content was sourced from clinicaltrials.gov

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