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The efficacy of third-generation EGFR-TKIs in patients with advanced, T790M-negative, EGFR-mutated NSCLC after progression on first- or second-generation EGFR-TKIs treatment: A retrospective study

The efficacy of third-generation EGFR-TKIs in patients with advanced, T790M-negative, EGFR-mutated NSCLC after progression on first- or second-generation EGFR-TKIs treatment: A retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096109
Enrollment
Unknown
Registered
2025-01-17
Start date
2025-02-01
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Non-small cell lung cancer

Interventions

non-third-generation (Non-3rd) EGFR-TKIs group:None
third-generation EGFR-TKIs treatment group:None

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed diagnosis of non-small cell lung cancer by histopathology; 2. Tumor tissue or body fluid samples tested negative for T790M by genetic testing; 3. First-line treatment with first- or second-generation EGFR-TKIs. 4. The patient has good compliance and can undergo regular follow-up visits; 5. The medical records are complete.

Exclusion criteria

Exclusion criteria: 1.Diagnosed with other malignancies within the last 5 years or a history of other malignancies, except for skin basal cell carcinoma, cervical carcinoma in situ, and breast ductal carcinoma in situ that have been effectively controlled; 2.Severe acute or chronic infections, including: Active infections requiring systemic treatment or systemic antibiotics; Known history of human immunodeficiency virus (HIV) infection and/or acquired immunodeficiency syndrome; patients with unknown HIV status who do not agree to undergo HIV testing are not eligible; Patients with active chronic hepatitis B or active hepatitis C infections, including those who test positive for hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibody at screening. Patients cannot be enrolled until further quantitative testing clearly rules out the presence of active hepatitis B or C infection requiring treatment (e.g., HBV DNA <= 2500 copies/mL or 500 IU/mL, HCV RNA = lower limit of detection); 3.Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
overall survival;Second progression-free survival (PFS2);

Secondary

MeasureTime frame
Incidence of adverse reactions;

Countries

China

Contacts

Public ContactShujun Li

Affiliated Hospital of Guangdong Medical University

guwu72@163.com+86 759 2386971

Outcome results

None listed

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