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NCT Number: NCT06248554

Adjuvant PD-1 Inhibitor for Patients With Early-stage Hepatocellular Carcinoma Following Microwave Ablation

For early-stage hepatocellular carcinoma, i.e. Barcelona Clinical Liver Cancer Stage 0, ablation is the standard treatment with a comparable prognosis and less risk of ablation compared with liver resection. However, ablation is demanding on the surgeon and patients often face early recurrence if ablation is not complete. Therefore, it is necessary to find reasonable adjuvant treatment to consolidate the effect of microwave therapy.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

Wuhan, 430000, China

Location status: Recruiting

Location contact

WanGuang D Zhang

CONTACT

[email protected]

+8613886195965

About this study

For early-stage hepatocellular carcinoma, i.e. Barcelona Clinical Liver Cancer Stage 0, ablation is the standard treatment with a comparable prognosis and less risk of ablation compared with liver resection. However, ablation is demanding on the surgeon and patients often face early recurrence if ablation is not complete. Therefore, it is necessary to find reasonable adjuvant treatment to consolidate the effect of microwave therapy. There is no consensus on postoperative adjuvant therapy, especially for the management of early-stage HCC. Most scholars believe that HCC in this period does not have high-risk factors for tumor recurrence, thus neglecting the role of adjuvant therapy. Early studies have found that microwave ablation can alter the tumor microenvironment, which is conducive to the action of immune checkpoint inhibitors such as PD-1 inhibitors and even has a synergistic anti-tumor effect. We therefore designed this prospective cohort study to explore the efficacy and safety of adjuvant PD-1 inhibitors after microwave surgery.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged 18-75 years
  • Pathological type is HCC, BCLC stage 0-A
  • No extrahepatic HCC
  • No radiographic recurrence at 2-4 weeks after ablation
  • Eastern Cooperative Oncology Group (ECOG) performing status of 0-1
  • Child-Pugh grade A or B and adequate hematologic and organ function

Exclusion criteria

  • Any history of other malignant tumors or recurrent HCC
  • Any preoperative treatment for HCC including local and systemic therapy
  • Any acute active infectious diseases, active or history of autoimmune disease, or immune deficiency
  • Any persistent serious ablation-related complications
  • Esophageal and/or gastric variceal bleeding within 6 months
  • Inability or refusal to comply with the treatment and monitoring
  • Participation in other clinical trials

Treatment and study plan

PD-1 Inhibitors

Drug

Patients in the intervention group received post-operative adjuvant PD-1 inhibitor therapy, 240 mg intravenously every three weeks for nine cycles

Primary outcomes

  1. Disease-free survival

    Time frame: From date of include in this research until the date of first documented recurrence or date of death from any cause, whichever came first, assessed up to 60 months

    Disease-free survival was defined as the period from inclusion in the study until tumor recurrence, death from any cause.

Secondary outcomes

  1. Overall survival

    Time frame: From date of include in this research until the date of death from any cause, whichever came first, assessed up to 60 months

    Overall survival was defined as the period from study inclusion until death from any cause.

  2. Adverse effects

    Time frame: 6 months

    Adverse reactions are defined as any reaction during treatment that is inconsistent with the purpose of the treatment.

Study contacts

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

WanGuang D Zhang

CONTACT

[email protected]

+8613886195965

Sponsors and collaborators

Lead sponsor

Chen Xiaoping

Other

Registry information

Official study title

Adjuvant PD-1 Inhibitor for Patients With Early-stage Hepatocellular Carcinoma Following Microwave Ablation: a Prospective Cohort Study

Important dates

Study start
2019
Primary completion
2024
Study completion
2025
First posted
Feb 8, 2024
Registry last updated
Dec 2, 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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