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Esophageal Artery Perfusion Chemotherapy Combined with Apatinib in the Treatment of Advancand Esophageal Carcinoma with Failure of Radiochemotherapy: A Prospective, Exploratory, Open, Single-center, One-arm Clinical Trial

Esophageal Artery Perfusion Chemotherapy Combined with Apatinib in the Treatment of Advancand Esophageal Carcinoma with Failure of Radiochemotherapy: A Prospective, Exploratory, Open, Single-center, One-arm Clinical Trial

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016882
Enrollment
Unknown
Registered
2018-06-30
Start date
2018-06-29
Completion date
Unknown
Last updated
2018-07-02

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

Conditions

Esophageal Carcinoma

Interventions

Case series:Esophageal cancer infusion chemotherapy combined with apatinib

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old; 2. Patients with advanced esophageal cancer diagnosed by pathological examination, stage II~IV of pathological staging, and patients with advanced esophageal cancer who failed radiotherapy and chemotherapy, have measurable lesions; 3. Life expectancy is expected to exceed 3 months; 4. Eastern Cooperative Oncology Group(ECOG) performance status=1; 5. Pregnancy tests for women of reproductive age must be negative; both men and women should agree to use effective contraception during treatment and within the next year; 6. Subjects with good compliance and followed up voluntarily participated in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. INR > 1.5, or underway anticoagulation therapy or known hemorrhagic diseases; 2. unstable coronary heart disease or recent myocardial infarction (within one year); 3. Recent infections required antibiotic treatment; 4. Patients with pulmonary insufficiency (MVV%/VC% = 50% and FVC% = 40%); 5. WBC 2mg/L); 7. AST and/or ALT> 5 ULN; 8. The DSA showed that the tumor blood supply artery contained the anterior spinal artery; the artery was too thin and the intubation was unsuccessful; 9. The comorbidity or social environment that may cause the subject to fail to follow the study plan or even jeopardize patient safety; 10. The patient is accompanied by other primary tumors.

Design outcomes

Primary

MeasureTime frame
overall survive;Disease Control Rate;Time To Progress;

Countries

China

Contacts

Public ContactWu Gang
wuganghenan2004@163.com+86 13938570175

Outcome results

None listed

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