Perihilar Cholangiocarcinoma Clinical Trial
Official title:
Prospective Multicentre Trial of Biliary Drainage Plus Hepatic Arterial Infusion Chemotherapy Versus Biliary Drainage Plus Best Supportive Care in Locally Advanced Perihilar Cholangiocarcinomas.
Verified date | May 2023 |
Source | Peking University |
Contact | Xiaodong Wang |
Phone | 18611586227 |
xiaodongw75[@]yahoo.com | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Recruiting |
Enrollment | 127 |
Est. completion date | December 31, 2025 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
China | Department of Interventional Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education),Peking University Cancer Hospital and Institute | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking University |
China,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Adverse effects | Toxicities were graded according to the Common Terminology Criteria for Adverse Events, version 4.0 | 6 months | |
Primary | Overall survival | Overall survival is measured from the date of first biliary drainage to death | 1 year | |
Secondary | Duration of jaundice remission | The time between remission of total bilirubin to less than 2 times of the upper limit of the normal value and time of rising again of bilirubin above more than 2 times of upper limit of the normal level. | 1 year |
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