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Completed

NCT Number: NCT05024513

Biliary Drainage Plus HAIC in Locally Advanced pCCA

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Interventional Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education),Peking University Cancer Hospital and Institute

Beijing, China

About this study

When a patient is not eligible for surgery, chemotherapy with gemcitabine and cisplatin can be considered for advanced biliary tract cancer. However, in the Advanced Biliary Tract Cancer, or ABC-02 trial in patients with pCCA, the efficacy of this regimen was not significantly higher than that of gemcitabine alone. Therefore, an optimal chemotherapeutic regimen has not been established for this subtype of cholangiocarcinoma. Currently, biliary drainage and stent placement remains to be the main palliative treatment choice, and the life expectancy is only 4-6 months. Previous single center prospective phase 2 trial showed that HAI with oxaliplatin and 5-fluorouracil was an encouraging treatment choice for advanced PCC due to its high tumor control, survival benefit, and low toxicity. So the multicenter prospective controlled trial was designed to explore and confirm the survival benefit of biliary drainage plus hepatic arterial infusion of oxaliplatin and 5-fluorouracil compared with biliary drainage plus best support care treatment in locally advanced pCCA patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Locally advanced perihilar cholangiocarcinoma proved by histology or cytology.
  • Locally advanced unresectable perihilar cholangiocarcinoma, decided by hepatobiliary doctor and radiologist.
  • Age from 18 years old to 80 years old.
  • The performance of Eastern Cooperative Oncology Group (ECOG) <2
  • Child-Pugh A or Child-Pugh B (≤ grade 7).
  • Expectant survival time ≥ 3 months.
  • Baseline blood count test and blood biochemical must meet following criteria:
  • Hemoglobin ≥ 90 g/L;
  • Absolute neutrophil count ≥ 1.5×10^9/L;
  • Blood platelet count ≥ 100×10^9/L;
  • Serum creatinine ≤ 1.5 times of ULN;
  • Albumin ≥ 30 g/L
  • Patients sign informed consent.

Exclusion criteria

  • Allergic to contrast agent.
  • Pregnant or lactational.
  • Allergic to 5-fluorouracil, or have metabolic disorder of 5-fluorouracil.
  • Previous systematic chemotherapy or radiotherapy.
  • Patients with complications such as bile leakage and bleeding after PTCD
  • N2 lymphatic metastasis, extrahepatic metastasis, or coinstantaneous a lot of malignant hydrothorax or ascites.
  • History of organ transplantation.
  • Coinstantaneous infection and need anti-infection therapy.
  • Coinstantaneous peripheral nervous system disorder or with history of obvious mental disorder and central nervous system disorder.
  • Diagnosed other kinds of malignant within 5 years, except for non-melanoma skin cancer and carcinoma in situ of cervix.
  • Without legal capacity.
  • Uncorrectable coagulation disorder.
  • 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.
  • Severe liver disease (like cirrhosis), renal disease, respiratory disease,unmanageable diabetes or other kinds of systematic disease.

Treatment and study plan

oxaliplatin and 5-fluorouracil

Drug

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.

Biliary drainage

Procedure

External biliary drainage, or biliary stent placement; Biliary stent placement plus Iodine-125 seed strands is allowed

Best supportive care

Other

Nutrition support, symptomatic treatment, and other supportive treatments

External biliary drainage

Procedure

External biliary drainage

Primary outcomes

  1. Overall survival

    Time frame: 1 year

    Overall survival is measured from the date of first biliary drainage to death

Secondary outcomes

  1. Duration of jaundice remission

    Time frame: 1 year

    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.

Other outcomes

  1. Adverse effects

    Time frame: 6 months

    Toxicities were graded according to the Common Terminology Criteria for Adverse Events, version 4.0

Sponsors and collaborators

Lead sponsor

Peking University

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Aug 27, 2021
Registry last updated
Dec 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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