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Efficacy and safety of anti-recurrence therapy with envafolimab in patients with different lymphatic vessel density at the junction of hepatocellular carcinoma after radical resection

Efficacy and safety of anti-recurrence therapy with envafolimab in patients with different lymphatic vessel density at the junction of hepatocellular carcinoma after radical resection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078081
Enrollment
Unknown
Registered
2023-11-28
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hepatocellular carcinoma (HCC)

Interventions

Low lymphatic vessel density group:None
High lymphatic vessel density group:None

Sponsors

The Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients with age of 18-65 years, including male and female 2.Treatment-naive patients, with BCLC stage 0 or A, received radical hepatectomy in The Second Affiliated Hospital of Kunming Medical University from December 1, 2023 to November 30, 2024. Postoperative pathology confirm: HCC with R0 resection, peripheral liver cirrhosis, MVI M0, and no risk factors for recurrence such as satellite nodular metastasis 3.ECOG score returned to 0-1 within 14 days after surgery 4.Child-Pugh score returned to Grade A within 14 days after surgery 5.Written informed consent

Exclusion criteria

Exclusion criteria: 1.Preoperative lymphocyte absolute value was less than 1.1×10^9/L 2.Patients with severe or life-threatening liver, kidney, cardiovascular and cerebrovascular diseases 3.Pregnant or have a family plan within one year of the start of treatment 4.Allergic to envafolimab 5.Other conditions were not suitable for inclusion judged by researchers

Design outcomes

Primary

MeasureTime frame
Recurrence-free survival;Overall survival;

Secondary

MeasureTime frame
Treatment-related adverse effects rate;Grade 3-4 adverse effects rate;

Countries

China

Contacts

Public ContactKe Yang

The Second Affiliated Hospital of Kunming Medical University

keyang1218@126.com+86 158 0887 5159

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026