Clinical trial · Interventional
Apatinib Combined With EGFR-TKI for Advanced Slow-progressed EGFR-TKI Resistant NSCLC
Apatinib Combined With Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors Used for the Advanced Slow-progressed Non Small Cell Lung Cancer Patients With EGFR-TKI Resistance
NCT03428022CI-TRIAL-00037941AFLCunknownPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Patients with advanced non-small cell lung cancer (NSCLC) who progress slowly after Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors(EGFR-TKI)resistance will be treated with Apatinib and EGFR-TKI. The primary objective is the disease progression free survival of the patients.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Apatinib | — | UNRESOLVED | — |
| EGFR-TKI | — | UNRESOLVED | — |
| NSCLC | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Apatinib(Tab. 500mg/d) combined with EGFR-TKI(as previously) | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Apatinib combined with EGFR-TKI
- description
- Apatinib(Tablet(Tab. )500millgram(mg)/day(d)) combined with EGFR-TKI(as previously)
- interventionNames
- Drug: Apatinib(Tab. 500mg/d) combined with EGFR-TKI(as previously)
Primary outcomes (1)
- measure
- PFS
- timeFrame
- 3 months
- description
- the disease progression free survival of patients
Secondary outcomes (2)
- measure
- OS
- timeFrame
- 8 months
- description
- overall survival
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Pathologically confirmed advanced (stage IV) non-squamous, non-small cell lung cancer with measurable lesions * Electronics Coordinating Grop(ECOG)score:0-2 * Expected survival over 3months * Hemoglobin(HB)≥90 gram(g)/liter(L);absolute neutrophil count(ANC)≥1.5×109/L;platelet(PLT)≥80×109/L;total-bilirubin(T-BIL)\<1.5 upper limit of normal value(ULN);alanine aminotransferase(ALT)and aspartate aminotransferase(AST)\<2.5 ULN;Cr≤1.25ULN Exclusion Criteria: * Brain metastases, meningococcal meningitis, patients with spinal cord compression with evidence of imaging (computed tomography(CT) / magnetic resonance imaging (MRI), et cetera(etc.)); * Uncontrolled hypertension (systolic blood pressure(BP)≥140 millimeter mercury column(mmHg) or diastolic BP ≥90 mmHg, despite optimal drug therapy); * Hemorrhoid dysfunction (inernational standard ratio(INR)\> 1.5 or prothrombin time (PT)\> ULN + 4 seconds or activated partial thromboplastin(APTT)\> 1.5 ULN) with bleeding tendency or undergoing thrombolytic or anticoagulant therapy; * Patients treated with anticoagulants or vitamin K antagonists such as warfarin, heparin, or the like; * Patients underwent major surgery or severe traumatic injury, fracture or ulcer in 4 weeks before study; * Urine routine urine protein ≥ +++, or confirmed 24 hours urinary protein content ≥ 1.0 g;
References
Publications (0)
Data not yet available
No reference posted for this study.