Tests third-generation EGFR drugs after surgery in early lung cancer patients
Observes EGFR-positive early lung cancer patients with high-risk features taking third-generation EGFR drugs.
Key facts
- Who runs it
- First Affiliated Hospital of Guangxi Medical University
- Where
- Nanning, ChinaSee the site
- Trial code
- Registry title
- A Non-interventional, Real-world Study on the Adjuvant Treatment of Chinese EGFR-positive Stage IA NSCLC Patients With High-risk Factors Using Third-generation EGFR-TKIs.
- Status
- Not yet recruiting
- People taking part
- 500 people, planned
- Started
- 1 Sept 2026
- Expected to end
- 31 Dec 2032
- Type of study
- Observational
- Treatments tested
- Third-generation EGFR-TKI
- Record updated
- 7 July 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with stage IA non-small cell lung cancer, an EGFR mutation and high-risk features, who have had or will have surgery and take a third-generation EGFR-TKI afterwards.
- Age
- 18 years or older
- Sex
- All sexes can join
- Disease stage
- Stage IA non-small cell lung cancer (8th edition of the AJCC staging system), confirmed under the microscope, with high-risk factors such as poor differentiation, lymphovascular invasion or spread through air spaces
- Earlier treatment
- No earlier treatment for the cancer that works through the whole body. Surgery already done or planned. Third-generation EGFR-TKI after surgery already given or planned
- Biomarker or test result
- EGFR mutation positive
Main reasons for not taking part
- Small cell lung cancer
- Another cancer that needs treatment
- Pregnant or breastfeeding women
- The researchers think the person should not take part
The registry criteria, word for word
Show all 10 criteriaShow less
Who can take part
- Age ≥ 18 years old
- Patients with IA-stage (8th edition of AJCC staging) non-small cell lung cancer (NSCLC) confirmed by histopathology and with high-risk factors
- EGFR mutation positive
- No previous systemic anti-tumor treatment
- Expected or already received surgical treatment
- Intended to receive or already received third-generation EGFR-TKI adjuvant therapy after surgery
Who cannot take part
- Small cell lung cancer
- With other malignant tumors that require treatment
- Pregnant or lactating women
- Those who the researchers consider not suitable to participate in this clinical trial
Where in China
- The First Affiliated Hospital of Guangxi Medical UniversityNanning, ChinaContact: Nuo YangNo longer taking part
About the trial
What the trial wants to find out
This study aims to evaluate the real-world effectiveness and safety of third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs)-such as osimertinib, aumolertinib, and furmonertinib-as adjuvant therapy for patients with early-stage non-small cell lung cancer (NSCLC) in China.
Read full original descriptionShow less
Approximately 500 eligible patients are planned to be enrolled. All participants must have been diagnosed with Stage IA NSCLC (according to the 8th edition of the AJCC staging system) following surgical resection, harboring EGFR-sensitive mutations, and presenting with high-risk recurrence factors (e.g., poor differentiation, lymphovascular invasion, and spread through air spaces).
This is a non-interventional, real-world study that does not alter physicians' original prescribing habits or clinical management strategies. Patients will receive standard treatment with third-generation EGFR-TKIs according to routine clinical practice (typically for a duration of three years). The research team will periodically collect follow-up data, with a primary focus on postoperative disease-free survival (DFS) and drug safety profiles.
Through this investigation, we seek to determine whether this specific population of high-risk early-stage patients can derive clinical benefit from postoperative targeted therapy. The findings are expected to provide evidence to support the development of future clinical guidelines.
The group in the trial
- Observational Group
Third-generation EGFR-TKI adjuvant therapy for Chinese patients with stage IA EGFR-positive NSCLC who have high-risk factors
Treatment: Third-generation EGFR-TKI
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- A Non-interventional, Real-World Study of Third-Generation EGFR-TKI Adjuvant Therapy in Chinese EGFR-Positive Stage IA Non-Small Cell Lung Cancer Patients With High-Risk Factors
- Plain-language title
- Tests third-generation EGFR drugs after surgery in early lung cancer patientsGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Record updated
- 7 July 2026