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NCT Number: NCT06487663

TACE Combined With Immune Checkpoint Inhibitors for Liver Malignant Tumors

This study will evaluate the efficacy and safety of TACE combined with immune checkpoint inhibitors to treat unresectable hepatocellular carcinoma.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tianjin Medical University Cancer Institute and Hospital

Tianjin, China

Location status: Recruiting

Location contact

Haipeng Yu, PhD

PRINCIPAL_INVESTIGATOR

Yu Zheng

CONTACT

[email protected]

0086-22-23340123

About this study

The specific operation of TACE is based on the CSCO Diagnosis and Treatment Guidelines for Primary Liver Cancer (2022 Edition). TACE is performed through microcatheters. After TACE, the coaxial catheter is retained in the hepatic artery or left or right hepatic artery branch. The specific body plan is oxaliplatin+calcium folinate+5-Fu (FOLFOX) (J Hepatol, 2018). Oxaliplatin 85mg/m2 was continuously injected through arterial pump for more than 4 hours on the first day. After HAIC is completed, remove the catheter and sheath. Repeat catheterization in the next treatment cycle.

Immune checkpoint inhibitors can be administered arterial starting after the first TACE treatment, q4w (± 3 days). If the situation requires, the arterial administration of ICI can be adjusted forward or backward for 7 days to adapt to TACE treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Confirmed diagnosis of HCC by histology/ cytology or clinical criteria
  • Sign informed consent
  • When screening for age, the age should be ≥ 18 years old
  • Eligible for TACE treatment
  • ECOG physical condition score is 0 or 1
  • No prior systemic therapy for HCC, especially immunotherapy
  • According to the following mRECIST criteria, at least one measurable intrahepatic lesion is suitable for repeated evaluation

Exclusion criteria

  • Have any history of kidney disease or nephrotic syndrome
  • Evidence of extrahepatic spread (EHS)
  • Cardiovascular diseases with clinical significance (such as activity), including unstable angina, ≥ grade 2 congestive heart failure, and arrhythmia with poor drug treatment control
  • Any condition representing a contraindication to TACE as determined by the investigators
  • Known genetic factors for bleeding or thrombosis; Any previous or current evidence indicating a tendency for bleeding
  • Individuals who have received immunotherapy (anti PD-1, anti PD-L1, or anti CTLA-4 treatment)
  • Previously received HAIC (hepatic artery infusion chemotherapy), TACE (hepatic artery chemoembolization), TAE (hepatic artery embolization), or TARE (hepatic artery radiation embolization)
  • Previously received systemic anti-cancer treatment for HCC ,ICC or liver metastasis.

Treatment and study plan

TACE with ICI

Procedure

Transcatheter hepatic artery chemoembolization and immune checkpoint inhibitors

Primary outcomes

  1. PFS

    Time frame: 3 years

    Progression free survival

  2. OS

    Time frame: 3 years

    Overall Survival

Secondary outcomes

  1. ORR

    Time frame: 3 years

    Objective response rate

Other outcomes

  1. TTP

    Time frame: 3 years

    Time to Progression (TTP) as Determined by Investigator

  2. DOR

    Time frame: 3 years

    Duration of Responses (DOR) as Determined by Investigator

  3. AE

    Time frame: Baseline up to approximately 48 months

    Percentage of Participants With Adverse Events

Study contacts

Contact information is provided by the study sponsor or research team.

Haipeng Yu

CONTACT

[email protected]

022-23340123 ext. 2701

Sponsors and collaborators

Lead sponsor

Tianjin Medical University Cancer Institute and Hospital

Other

Registry information

Official study title

Transcatheter Hepatic Artery Chemoembolization Combined With Immune Checkpoint Inhibitors for Liver Tumors

Acronym: TIKET

Important dates

Study start
2020
Primary completion
2025
Study completion
2026
First posted
Jul 5, 2024
Registry last updated
Jul 5, 2024

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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