Skip to content

Apatinib combined with continuous hepatic arterial infusion of oxaliplatin and raltitrexed in hepatocellular carcinoma with extrahepatic spread: a prospective study

Apatinib combined with continuous hepatic arterial infusion of oxaliplatin and raltitrexed in hepatocellular carcinoma with extrahepatic spread: a prospective study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029082
Enrollment
Unknown
Registered
2020-01-13
Start date
2020-01-20
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Hepatocellular Carcinoma

Interventions

single arm:Oral apatinib combined with continuous hepatic arterial infusion of oxaliplatin and raltitrexed

Sponsors

Fujian Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Ages 18 to 70 years, (2) The diagnosis of hepatocellular carcinoma based on the recommendation of the American Association for the Study of Liver Diseases, (3) The patient should be a BCLC stage C patient with extrahepatic metastasis, and a person who has progressed or is unable to receive molecular targeted drug therapy such as Solafini. (4) When entering the study, the patient should be stopped for more than 4 weeks. (5) There is at least one measurable lesion that meets the RECIST v1.1 standard; (6) Child-Pugh class: A or B. (7) ECOG score 0-2. (8) An estimated survival period of more than 2 months. (9) Bone marrow function (hemoglobin >= 10 g/dL, leukocyte >= 3,000µL, platelet>= 75,000µL), liver function (bilirubin <= 3 mg/dL, aminotransferase <= 200 U/L), kidney function (muscle liver <= 390µmol/L). The coagulation function is basically normal.

Exclusion criteria

Exclusion criteria: (1) Decompensation of liver function (including uncontrolled ascites, hepatic encephalopathy, acute or recent gastrointestinal bleeding within 2 weeks). (2) Acute infection or sepsis. (3) During pregnancy. (4) Patients with cardiac insufficiency or poor lung function. (5) The life expectancy is less than three months. (6) Brain metastases.

Design outcomes

Primary

MeasureTime frame
Tumor response;

Countries

China

Contacts

Public ContactShiguang Chen

Fujian Cancer Hospital

sghcen207@163.com+86 15659996166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026