Transarterial Infusion of PD-1 Antibody Plus TACE-HAIC for Unresectable HCC: a Single-arm, Phase 2 Clinical Trial

Last updated: April 21, 2021
Sponsor: Sun Yat-sen University
Overall Status: Active - Recruiting

Phase

2

Condition

Abdominal Cancer

Hepatic Fibrosis

Carcinoma

Treatment

N/A

Clinical Study ID

NCT04814030
B2021-060
  • Ages 18-75
  • All Genders

Study Summary

Hepatocellular carcinoma (HCC) is a common disease in East Asia. Less than 20% of newly diagnosed patients can undergo radical resection. For those with unresectable BCLC C stage, transarterial chemotherapy and targeted therapy are recommend to prolong survival. Recently, FOLFOX (Oxaliplatin and 5-fluorouracil) based hepatic artery infusion chemotherapy (HAIC) exhibited high response rate for unresectable HCC. Transartery infusion of agents provide promising outcome when compared systemic infusion. Furthermore, our pilot study showed TACE combined HAIC (TACE-HAIC) had better tumor response, with low progression disease rate. Whether TACE-HAIC plus hepatic artery infusion PD-1 antibody would improve survival for unresectalbe BCLC C stage patients is still unknown. A single arm, phase 2 clinical trial is aimed to answer this question.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • BCLC C stage with unresectable diseasehigh-recurrence risk factor;
  • Child-Pugh A or B (7 score) liver function;
  • Anticipated survival more than 3 moths

Exclusion

Exclusion Criteria:

  • Pregnant woman or sucking period;
  • With other malignant cancer;
  • Received anti-HCC therapy before this study

Study Design

Total Participants: 80
Study Start date:
April 20, 2021
Estimated Completion Date:
December 30, 2022

Connect with a study center

  • Sun Yat-sen University Cancer Center

    Guangzhou, Guangdong 510060
    China

    Active - Recruiting

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