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Bevacizumab combined with afatinib for first-line treatment of locally advanced or advanced EGFR mutation-positive NSCLC patients: the effectiveness and safety database management platform construction project

Bevacizumab combined with afatinib for first-line treatment of locally advanced or advanced EGFR mutation-positive NSCLC patients: the effectiveness and safety database management platform construction project

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034451
Enrollment
Unknown
Registered
2020-07-05
Start date
2020-07-06
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

NSCLC

Interventions

Sponsors

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old; 2. Patients with locally advanced or advanced (stage IIIB/stage IV) or relapsed non-squamous non-small cell lung cancer confirmed by histopathology; 3. The patient has not received systematic treatment for advanced or relapsed non-squamous non-small cell lung cancer; 4. Provide detectable specimens (tissue or pleural effusion or blood specimens) for genotype testing before entering the group. EGFR sensitive mutation test results are required to be positive (except for drug resistance mutation EGFR-T790M test results that are positive); 5. The subjects voluntarily joined the study, signed an informed consent form, had good compliance, and cooperated with follow-up.

Exclusion criteria

Exclusion criteria: 1. Histopathological type is small cell lung cancer or lung squamous cell carcinoma or mixed non-small cell lung cancer containing small cell lung cancer or lung squamous cell carcinoma; 2. Patients who have received any systemic anti-tumor treatment in the past; 3. Genetic testing results of patients with EGFR-T790M resistance mutation, ALK rearrangement or ROS1 fusion; 4. Patients who are receiving anti-tumor therapy from other systems; 5. Subjects with previous malignant tumors should be excluded unless complete remission is achieved at least 2 years before enrollment in the study and no other treatment is required during the study period; 6. People with multiple factors that affect oral medications (such as inability to swallow, post-gastrointestinal resection, chronic diarrhea, and intestinal obstruction, etc.); 7. Active lung disease (interstitial pneumonia, pneumonia, obstructive pulmonary disease, asthma) or active tuberculosis; 8. Have any uncontrollable clinical problems.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
OS;ORR;DCR;

Countries

China

Contacts

Public ContactXingsheng Hu

National Cancer Center /Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

huxingsheng66@163.com+86 13641361385

Outcome results

None listed

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