Hepatocellular Carcinoma
Conditions
Brief 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, less than 20% of newly diagnosed patients can undergo radical resection. Our latest study showed that 48% potentially resectable HCC received hepatectomy after transarterial chemoembolization plus FOLFOX-based chemotherapy infusion (TACE-HAIC) treatment. Recently, several clinical trials (LEAP-002) showed that PD-1 antibody and Lenvatinib had an ORR of 36% for advanced patients. The combination of TACE-HAIC with PD-1 antibody and lenvatinib, theoretically can significantly decrease the tumor burden and increase the hepatectomy rate. However, this hasn't been verified in clinical application. To identify a more effective and safety way for treating potentially resectable HCC patients, this study is designed to investigate TACE-HAIC plus PD-1 antibody and Lenvatinib will increase the resection rate for those patients.
Interventions
DRUGPD-1 inhibitor
systemic PD-1 antibody (Sintilimab) and lenvatinib plus transarterial chemobolization and FOLFOX-based chemotherapy infusion
Sponsors
Sun Yat-sen University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
systemic PD-1 antibody and lenvatinib plus TACE-HAIC for potential resectable HCC
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Diagnosed as potentially resectable with consensus by the panel of liver surgeons * stage BCLC A/B/C, without extra-hepatic involvement * 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, or PD-1 antibody
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| conversion rate to resection | 12 month | The conversion rate to resection among all the enrolled patients |
Countries
China
Contacts
Primary ContactJiliang Qiu
Outcome results
None listed