Skip to content

Prospective study of oxaliplatin combined with retitrexed continuous hepatic artery infusion in the treatment of advanced primary liver cancer

Prospective study of oxaliplatin combined with retitrexed continuous hepatic artery infusion in the treatment of advanced primary liver cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17014182
Enrollment
Unknown
Registered
2017-12-27
Start date
2017-12-25
Completion date
Unknown
Last updated
2018-01-08

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

Conditions

Hepatocellular Carcinoma

Interventions

Case series:continuous hepatic artery infusion of oxaliplatin combined with retitrexide

Sponsors

Fujian Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. patients with liver cancer diagnosis of AASLD and EASL HCC; 2. based on the guidelines for the management of patients should be treated with conventional transcatheter arterial chemoembolization for patients with stage C or BCLC for intrahepatic diffuse multiple lesions and conventional chemoembolization therapy expected arteriovenous fistula in patients with BCLC B; 3. patients. Before local treatment such as TACE, RFA, radiotherapy, or systemic therapy such as molecular targeted drug therapy (Sola Feeney, apatinib etc.), intravenous chemotherapy, can also be incorporated in the study, as long as the focus of premenstrual treatment has no progress, the local treatment indications. In addition to patients when they entered the study period the treatment should be stopped for more than 4 weeks. The patients in surgery after recurrence and no TACE treatment indications can also be incorporated into the tumor stage. Based on the hepatic arterial infusion chemotherapy of tumor present situation; 4. the patient's should be between the ages of 18-75 years of bone; 5. Spinal cord function (Hb = 10 g/dL, WBC = 3000/ L, platelet count or 75000/L), liver function (serum bilirubin = 3mg/dL, U/L = 200), renal function (creatinine less than or equal to 390 Mu mol /L). The coagulation function is basically normal; 6. the PS score of 2 or less; 7. can obtain informed consent of patients or their families.

Exclusion criteria

Exclusion criteria: 1. decompensation of liver function (including ascites uncontrolled, hepatic encephalopathy); 2. Acute or recent Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage / Gastrointestinal Hemorrhage within 2 weeks; 3. extensive extrahepatic metastases.

Design outcomes

Primary

MeasureTime frame
Tumor response;

Countries

China

Contacts

Public ContactYu Wenchang

Department of Interventional Oncology, Fujian Cancer Hospital

sgchen207@163.com+86 13599962209

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 18, 2026