Clinical trial

Prospective Multicentre Trial of Biliary Drainage Plus Hepatic Arterial Infusion Chemotherapy Versus Biliary Drainage Plus Best Supportive Care in Locally Advanced Perihilar Cholangiocarcinomas.

Name
DRAIC
Description
Biliary drainage and stent placement remains to be the main palliative treatment choice for advanced perihiliar cholangiocarcinoma (pCCA), and the life expectancy is only 4-6 months. Previous single center prospective phase 2 trial showed that hepatic arterial infusion chemotherapy (HAIC) with oxaliplatin and 5-fluorouracil was an encouraging treatment choice for advanced pCCA due to its high tumor control, survival benefit, and low toxicity. Thus, the multicenter prospective controlled trial was designed to explore and confirm the survival benefit of biliary drainage plus hepatic arterial infusion chemotherapy with oxaliplatin and 5-fluorouracil compared with biliary drainage plus best support care treatment in locally advanced pCCA patients.
Trial arms
Trial start
2021-11-01
Estimated PCD
2024-12-31
Trial end
2025-12-31
Status
Recruiting
Phase
Early phase I
Treatment
oxaliplatin and 5-fluorouracil
Intra-arterial chemotherapy consisted of Oxaliplatin (40mg/m2 for 2 hours), 5-fluorouracil (800 mg/ m2 for22 hours) on days 1-3 every 4 weeks.
Arms:
BD-HAIC (Biliary drainage & HAIC)
Biliary Drainage
External biliary drainage, or biliary stent placement; Biliary stent placement plus Iodine-125 seed strands is allowed
Arms:
BD-BSC (Biliary Drainage & Best supportive care)
Best Supportive Care
Nutrition support, symptomatic treatment, and other supportive treatments
Arms:
BD-BSC (Biliary Drainage & Best supportive care)
External biliary drainage
External biliary drainage
Arms:
BD-HAIC (Biliary drainage & HAIC)
Size
127
Primary endpoint
Overall survival
1 year
Eligibility criteria
Inclusion Criteria: 1. Locally advanced perihilar cholangiocarcinoma proved by histology or cytology. 2. Locally advanced unresectable perihilar cholangiocarcinoma, decided by hepatobiliary doctor and radiologist. 3. Age from 18 years old to 75 years old. 4. The performance of Eastern Cooperative Oncology Group (ECOG) \<2 5. Child-Pugh A or Child-Pugh B (≤ grade 7). 6. Expectant survival time ≥ 3 months. 7. Baseline blood count test and blood biochemical must meet following criteria: 1. Hemoglobin ≥ 90 g/L; 2. Absolute neutrophil count ≥ 1.5×10\^9/L; 3. Blood platelet count ≥ 100×10\^9/L; 4. Serum creatinine ≤ 1.5 times of ULN; 5. Albumin ≥ 30 g/L 8. Patients sign informed consent. Exclusion Criteria: 1. Allergic to contrast agent. 2. Pregnant or lactational. 3. Allergic to 5-fluorouracil, or have metabolic disorder of 5-fluorouracil. 4. Previous systematic chemotherapy or radiotherapy. 5. Patients with complications such as bile leakage and bleeding after PTCD 6. N2 lymphatic metastasis, extrahepatic metastasis, or coinstantaneous a lot of malignant hydrothorax or ascites. 7. History of organ transplantation. 8. Coinstantaneous infection and need anti-infection therapy. 9. Coinstantaneous peripheral nervous system disorder or with history of obvious mental disorder and central nervous system disorder. 10. Diagnosed other kinds of malignant within 5 years, except for non-melanoma skin cancer and carcinoma in situ of cervix. 11. Without legal capacity. 12. Uncorrectable coagulation disorder. 13. Obvious abnormal in ECG or obvious clinical symptoms of heartdisease, like congestive heart failure (CHF), coronary heart disease with obvious clinical symptoms, unmanageable arrhythmia and hypertension. 14. Severe liver disease (like cirrhosis), renal disease, respiratory disease,unmanageable diabetes or other kinds of systematic disease.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 127, 'type': 'ESTIMATED'}}
Updated at
2024-01-10

1 organization

1 product

1 indication

Organization
Peking University