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Neoadjuvent therapy of furmonertinib for locally advanced lung adenocarcinoma with EGFR mutation: a prospective single arm, multicenter clinical trial

Neoadjuvent therapy of furmonertinib for locally advanced lung adenocarcinoma with EGFR mutation: a prospective single arm, multicenter clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076712
Enrollment
Unknown
Registered
2023-10-17
Start date
2023-10-17
Completion date
Unknown
Last updated
2023-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lung adenocarcinoma

Interventions

intervention:Furmonertinib

Sponsors

Department of thoracic surgery, Tongji hospital, Tongji medical college, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1- Age range: 18-70 years, both males and females are eligible. 2- Locally advanced lung adenocarcinoma confirmed by pathology, clinically staged as T3-4N0-2M0. 3- Positive for EGFR sensitive gene mutations, specifically EGFR 19 deletion mutation and EGFR 21 L858R mutation. 4- No previous exposure to radiotherapy or chemotherapy. 5- ECOG PS (Eastern Cooperative Oncology Group Performance Status): 0-1 points. 6- Subjects must voluntarily participate in this study, sign an informed consent form, demonstrate good compliance, and cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1-History of malignancy. 2-Presence of single or multiple distant metastases. 3-Poorly controlled heart diseases or symptoms, such as: a. heart failure(NYHA class 2 or higher). b. Unstable angina. c. Myocardial infarction within the past year. d. Clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention. 4-Severe COPD (Chronic Obstructive Pulmonary Disease), FEV1 (Forced Expiratory Volume in one second) < 0.8L, FEV1% < 50%.

Design outcomes

Primary

MeasureTime frame
ORR;

Secondary

MeasureTime frame
R0 rate;MPR;mPFS;

Countries

China

Contacts

Public ContactBo Ai

Department of thoracic surgery, Tongji hospital, Tongji medical college, Huazhong University of Science and Technology

tjaibo@126.com+86 134 7603 8820

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026