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Gefitinib plus pemetrexed combined with bevacizumab or carboplatin in first-line treatment of stage IV EGFR mutant non-squamous non-small cell lung cancer.

Gefitinib plus pemetrexed combined with bevacizumab or carboplatin in first-line treatment of stage IV EGFR mutant non-squamous non-small cell lung cancer.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043395
Enrollment
Unknown
Registered
2021-02-13
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

Lung Cancer

Interventions

Treatment Group:Gefitinib plus pemetrexed and bevacizumab
Control Group:Gefitinib plus pemetrexed and carboplatin

Sponsors

Shandong Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged >= 18 and <= 75; 2. Patients whose life expectancy exceeds 3 months; 3. Patients with at least one measurable focus other than brain; 4. NSCLC patients with stage IV non squamous cells confirmed by histology and living cytology; 5. ECOG score 0-1; 6. Never accept any systemic anti-tumor treatment; 7. EGFR mutation was positive (including 19del, L858R, g719a, g719c, G719S, l861q); 8. No brain metastasis, or with no symptomatic brain metastases, or symptomatic brain metastases after treatment was stable.

Exclusion criteria

Exclusion criteria: 1. Patients with mixed NSCLC with squamous cell morphology; 2. Mixed lung cancer patients with small cell carcinoma, neuroendocrine carcinoma and sarcoma; 3. EGFR non sensitive mutation or EGFR non mutation patients; 4. Patients with meningioma, meningeal metastases, or unstable brain metastases; 5. Patients who have received chemotherapy or EGFR-TKIs in the past; patients who have received adjuvant or neoadjuvant treatment and the last treatment to recurrence time <= 6 months.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
OS;ORR;DCR;TTR;DOR;Adverse events;

Countries

China

Contacts

Public ContactLiu Jie

Shandong Cancer Hospital

lj691012@126.com+86 15553119051

Outcome results

None listed

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