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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

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
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127214
Enrollment
Unknown
Registered
2026-06-26
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Histopathologically confirmed EGFR mutation-positive stage Ia non-small cell lung cancer (NSCLC) with high-risk factors

Interventions

Three-generation EGFR-TKI adjuvant therapy for Chinese patients with stage IA EGFR-positive NSCLC who have high-risk factors:NA

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 18 years old; 2. Patients with IA-stage (8th edition of AJCC staging) non-small cell lung cancer (NSCLC) confirmed by histopathology and with high-risk factors; 3. EGFR mutation positive; 4. No previous systemic anti-tumor treatment; 5. Expected or already received surgical treatment; 6. Intended to receive or already received third-generation EGFR-TKI adjuvant therapy after surgery.

Exclusion criteria

Exclusion criteria: 1. Small cell lung cancer; 2. With other malignant tumors that require treatment; 3. Pregnant or lactating women; 4. Those who the researchers consider not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
3-Years Disease-Free Survival rate;

Secondary

MeasureTime frame
5-Years Disease-Free Survival rate;Disease-free survival(DFS);5 years Overall Survival;3-years Overall Survival;Overall Survival;The type, frequency and severity of adverse events during treatment (TEAE) and treatment-related adverse events (TRAE);

Countries

China

Contacts

Public ContactYang Nuo

The First Affiliated Hospital of Guangxi Medical University

yangnuogxmu@163.com+86 771 535 6708

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026