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Real world study on second-line treatment of EGFR positive non-small cell lung cancer with apatinib and gefitinib

Real world study on second-line treatment of EGFR positive non-small cell lung cancer with apatinib and gefitinib

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039231
Enrollment
Unknown
Registered
2020-10-22
Start date
2020-10-10
Completion date
Unknown
Last updated
2021-01-25

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

Conditions

Lung cancer

Interventions

Case series:Apatinib combined with gefitinib

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old, male or female; 2. Egfr-positive patients with stage II, III, and IV NSCLC, including: patients who can continue to use EGFR-TKIS after progression of first-line EGFR-TKIS treatment; 3. T790M mutation was negative and cMET amplification was negative; 4. Participate in the study voluntarily and sign the informed consent; 5. The researchers think there are benefits; 6. ECOG PS 0-2.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients with contraindications associated with apatinib or EGFR-TKIS (e.g., active bleeding, ulcers, perforation of the intestine, intestinal obstruction, uncontrolled hypertension, grade III-IV cardiac insufficiency, 30 days after major surgery, and severe hepatic and renal insufficiency); 3. The doctor considers the patient who is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Countries

China

Contacts

Public ContactWang Ke

West China Hospital, Sichuan University

1693123369@qq.com+86 18980602252

Outcome results

None listed

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