TACE-HAIC Plus Lenvatinib for Patients With Unresectable HCC: an Open-label Single-arm Phase 2 Trial

  • STATUS
    Recruiting
  • End date
    Aug 30, 2023
  • participants needed
    60
  • sponsor
    Yunfei Yuan
Updated on 29 September 2021
cancer
liver transplant
cirrhosis
folfox
TACE
chemoembolization
antineoplastic
hepatic arterial infusion
lenvatinib
hepatectomy

Summary

Hepatocellular carcinoma (HCC) is one of the most commonly malignant tumors around the world. Hepatic resection or liver transplantation is the radical method to cure the disease. However, due to multiple tumors or poor hepatic function reserve in cirrhosis, surgical treatment is suitable for early-stage and well reserved liver function patients. Therefore, in clinical practice, transarterial chemoembolization (TACE) is a preferential and standard treatment of unresectable HCC. TACE has been proved to provide outstanding efficacy for treating advanced stage HCC patients. However, TACE is associated with a high rate of treatment failure for advanced HCC patients. EACH trial opened the door to FOLFOX-based system chemotherapy for advanced HCC patients. Recently, investigators have showed that hepatic arterial infusion of FOLFOX-based chemotherapy (HAIC) was safe and efficient for advanced HCC patients. The combination of TACE with HAIC (TACE-HAIC) was proved to increase the local doses of chemotherapeutic agents in the liver, reduce the viability of HCC cells and increase the hepatectomy rate in our previous study.

Levatinib is a new treatment and offers relative high overall response rate for advanced HCC, which was approved in China and Japan. However, whether the combination of TACE-HAIC and Lenvatinib would increse tumor control for unresectable patients is still unknown. Thus, this single arm, phase 2 study is designed to analyze the safety and efficacy TACE-HAIC plus Lenvatinib for patients with unresectalbe HCC.

Details
Condition Transarterial Chemoembolization, HEPATIC NEOPLASM, HEPATOCELLULAR CARCINOMA, Liver Cancer, TACE, Adenocarcinoma, liver cell carcinoma, Malignant Adenoma
Treatment TACE-HAIC plus lenvatinib
Clinical Study IdentifierNCT04531228
SponsorYunfei Yuan
Last Modified on29 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Age 18-75 years
The diagnosis of HCC was based on the diagnostic criteria for HCC used by the European Association for the Study of the Liver (EASL)
unresectable disease, stage BCLC B/C
No previous anti-HCC treatment
Eastern Co-operative Group performance status 2 or less
Liver function: Child's A or B (score < 7)

Exclusion Criteria

Evidence of hepatic decompensation including ascites, gastrointestinal bleeding or hepatic encephalopathy
underlying serve cardiac or renal diseases
Known or suspected allergy to the investigational agent or any agent given in association with this trial
Patients ineligible for hepatic artery embolization
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