Hepatocellular Carcinoma
Conditions
Keywords
sorafenib, intraarterial infusion chemotherapy, Low dose FP, cisplatin, fluorouracil
Brief summary
The purpose of this study is to determine the recommended dose of the combination therapy of sorafenib with hepatic arterial infusion of low dose cisplatin and fluorouracil on patients with advanced hepatocellular carcinoma (Phase I), and to evaluate the efficacy of this combination therapy in the recommended dose (Phase II).
Detailed description
In Phase I, there will be 9 to 18 patients enrolled. Cohorts of 3 to 6 patients will receive escalated dose of cisplatin and fluorouracil until the MTD is reached. There will be no intra-patient dose escalation. Sorafenib will be administered orally at a dose of 400mg bid for 28 days in the all patients. Cisplatin at the dose of 10-20mg/m2 will be administered at day 1 and day8, and fluorouracil at the dose of 170-330mg/m2 will be administered continuously at day1-day5, and day8-day12 via the implanted catheter system. A cycle is defined as 28 days and 3 cycles of this combination therapy will be continued. At the end of each cycle, adverse effect will be evaluated and dose escalation will be determined. In Phase II, there will be 28 patients enrolled. Time to progression of this combination therapy at the recommended dose will be evaluated.
Interventions
DRUGsorafenib, cisplatin, fluorouracil
Sorafenib will be administered orally at a dose of 400 mg bid for 28 days in the all patients. Cisplatin at the dose of 10-20 mg/m2 will be administered at day 1 and day8, and fluorouracil at the dose of 170-330 mg/m2 will be administered continuously at day 1-day 5, and day8-day12 via the implanted catheter system. A cycle is defined as 28 days and 3 cycles of this combination therapy will be continued.
Sponsors
Kindai University
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. 20 Years and older. 2. Life expectancy of at least 12 weeks at the pre-treatment evaluation. 3. Advanced hepatocellular carcinoma with histological evidence on a biopsy specimen, or typical findings by dynamic CT or CT during hepatic arteriography/arterioportography. 4. Not suitable for resection or local ablation therapy or transcatheter arterial chemoembolization. 5. One treatment of hepatic arterial infusion chemotherapy without implanted catheter system is allowed. 6. ECOG Performance status of 0 or 1. 7. Cirrhotic status of Child-Pugh class A or B. 8. Adequate bone marrow, liver and renal function, as assessed by the following laboratory requirements: * Hemoglobin 8.5 g/dl * Granulocytes 1500/μL * Platelet count 50,000 /μL * PT-INR 2.3 or PT 6 seconds above control * Total serum bilirubin 2 mg/dl * AST(SGOT) and ALT(SGPT) 5 × upper limit of normal * Serum creatinine 1.5 × upper limit of normal * Amylase 5 × upper limit of normal 9. Written Informed Consent must be obtained.
Exclusion criteria
1. Previous malignancy (except for cervical carcinoma in situ, adequate treated basal cell carcinoma, or superficial bladder tumors \[Ta, Tis and T1\], early gastric cancer, or other malignancies curatively treated \> 3 years prior to entry 2. Renal failure 3. Any heart disease as follows * Congestive heart failure defined as NYHA class III or IV * Active coronary artery disease or ischemic heart disease such as cardiac infarction within 6 months prior to screening * Serious cardiac arrhythmia * Serious hypertension 4. Active clinically serious infections. 5. Active chicken pox. 6. Auditory disorder. 7. Known history of HIV infection. 8. Known metastatic or meningeal tumors. 9. Extrahepatic tumor spread. 10. History of seizure disorder. 11. Clinically significant gastrointestinal bleeding within 4 weeks prior to study entry. 12. Embolization or infarction such as transient ischemic disease, deep vein thrombosis, pulmonary embolization). 13. Any history of treatment as follows: * Treatment with the agent which induces CYP3A4 * Surgical procedure within 4 weeks prior to start of study drug * History of organ allograft 14. Patients unable to swallow oral medications. 15. Gastrointestinal disease that may affect to the absorption of drug or pharmacokinetics. 16. Medication that may affect to the absorption of drug or pharmacokinetics. 17. Any disease or disorder that may affect the evaluation of study drug. 18. Entry to the other clinical trial within 4 weeks prior to entry to this study. 19. Pregnant or breast-feeding patients. 20. Known allergy to the investigational agent or any agent given in association with this trial. 21. Substance abuse, medical, psychological or social conditions that, in the judgment of the investigator, is likely to interfere with the patient's participation in the study or evaluation of the stuy results. 22. Any condition that is unstable or could jeopardize the safety of the patient and its compliance in the study, in the investigator's judgment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dose limiting toxicity in phase I and Time to progression in Phase II | Every 4 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Phase I and II: Overall survival (OS) | Every day |
| Phase I and II: Progression free survival (PFS) | Every four weeks |
| Phase I: Time to progression (TTP) | Every four weeks |
| Phase I and II: Response Rate (RR) | Every four weeks |
| Phase I and II: Adverse effect (AE) | Every four weeks |
Countries
Japan
Outcome results
None listed