Clinical trial · Interventional
Apatinib and Chemotherapy Sequential Treatment With Cervical Cancer
A Phase II Clinical Trial Study on Apatinib and Chemotherapy Sequential Treatment With Advanced Metastatic Cervical Cancer
NCT03029013CI-TRIAL-00025583unknownN/AClinicalTrials.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)
The study is the single arm and single center clinical trials,We conduct the phase II clinical trial to further explore the efficacy and safety of Apatinib and chemotherapy sequential treatment with advanced recurrence of metastatic cervical cancer
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Apatinib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- experimental group
- description
- Apatinib and chemotherapy
- interventionNames
- Drug: Apatinib
Primary outcomes (1)
- measure
- Progression free survival
- timeFrame
- 24 months
Secondary outcomes (1)
- measure
- overall survival
- timeFrame
- 24 months
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 25 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * The pathological diagnosis of recurrent or metastatic cervical cancer; * Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 1; * Life expectancy of more than 3months; * With normal marrow, liver and renal function: * blood routine examination :HB≥90g/L,ANC ≥1.5×10\*9/L,PLT≥80×10\*9/L; * Biochemical examination: total bilirubin (TBil) of ≤1.5 upper normal limitation (UNL),alanine aminotransferase (ALT) and aspartate aminotransferase (AST) of ≤2.5 UNL or ≤5 UNL ,acreatinine (Cr) of ≤ 1.25 UNL; creatinine clearance rate ≥ 45ml/min (Cockcroft-Gault); * With written informed consent signed voluntarily by patients themselves . * With good compliance and agree to accept follow-up of disease progression and adverse events. Exclusion Criteria: * Uncontrolled hypertension * Suffered from grade II or above myocardial ischemia or myocardial infarction, uncontrolled arrhythmias * With abnormal coagulation function, bleeding tendency or treating with thrombolysis and anticoagulation * History of clinically relevant major bleeding event (e.g. gastrointestinal hemorrhage, bleeding ulcer, occult blood ≥ (++), and vasculitis) =\< 3 months prior to randomization; * uncured the wound or fracture * Centrally located tumors of local invasion of major blood vessels, or Researchers think that patients may invade the important blood vessels and cause fatal bleeding (CT or MRI); * Factors affecting the oral medication (e.g. inability to swallow, chronic diarrhea and intestinal obstruction); * Urine protein \>++, or urine protein in 24 hours\> 1.0g * Accumulation of coelomic fluid (e.g. pleural effusion, ascites fluid, cardiac effusion) requiring treatment * History of uncontrolled psychotropic drug abuse or mental disorders; * Prior VEGFR inhibitor treatment ; * Other malignancy within Before or at the same time other than basal cell skin cancer, or carcinoma in situ of the cervix;
References
Publications (0)
Data not yet available
No reference posted for this study.