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Study on the Combined Treatment of Hepatocellular Carcinoma With Envafolimab, Suvemcitug and HAIC Conversion (HCC)

An Exploratory Study on the Use of Envafolimab Combined With Suvemcitug and HAIC for the Conversion Therapy of Potentially Resectable Hepatocellular Carcinoma

This study is a single-center, exploratory clinical trial. Eligible patients with liver cancer, after signing the informed consent form, will be screened and enrolled. They will receive a 3-cycle conversion treatment with Envafolimab combined with Suvemcitug and HAIC. During the treatment process, clinical tumor imaging assessment will be conducted using RECIST V1.1. Imaging evaluations will be performed before treatment and at the end of the 3rd cycle of treatment (±3 days). Subsequently, an MDT assessment will be conducted to determine if the surgical resection criteria are met. If the criteria are met, a radical surgery will be performed based on the subject's wishes and postoperative treatment will be provided. If the criteria are not met, the study will be decided to continue with the original treatment plan or another treatment plan. CTCAE 5.0 will be used for safety assessment. Adverse events will be recorded throughout the study period until 30 days after the end of treatment (for severe adverse events or adverse events related to Envovalimab, the recording period will be extended to 90 days after the end of treatment). To ensure study safety, 3 patients will be enrolled as a safety introduction cohort first, and a 3-cycle conversion treatment with Suvemcitug combined with Envafolimab and HAIC will be used. If a DLT occurs, 3 more patients will be enrolled. If the overall DLT does not exceed 1/3, the original treatment plan will be maintained for the study. If the overall DLT is greater than 1/3, the drug related to the DLT will be re-evaluated and the dose will be adjusted.

研究概览

研究类型

介入性

注册 (估计的)

35

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Huikai Li,MD Huikai Li,MD
  • 电话号码:86+18622228639
  • 邮箱:vianvianvip@163.com

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Sign a written informed consent form before enrollment;
  2. Age 18-75 years old;
  3. Diagnosed with hepatocellular carcinoma (HCC) by clinical assessment;
  4. Patients with stage IV or III unresectable liver cancer;
  5. Have measurable lesions (according to the RECIST 1.1 standard, non-lymph node lesions with CT scan diameter ≥ 10 mm, lymph node lesions with CT scan diameter ≥ 15 mm);
  6. Have not received any systemic anti-tumor treatment before, including but not limited to immunotherapy, targeted therapy, and anti-tumor traditional Chinese medicine treatment;
  7. Child-Pugh score ≤ 7 points;
  8. Have sufficient organ function; 1) Blood routine: White blood cell (WBC) ≥ 3.5 × 10^9/L, absolute neutrophil count (ANC) 1.5 × 10^9/L, platelet (PLT) ≥ 100 × 10^9/L, hemoglobin (HGB) ≥ 90 g/L; 2) Liver function: Serum total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × ULN; 3) Kidney function: Serum creatinine (Cr) ≤ 1.5 × ULN, or creatinine clearance rate ≥ 50 mL/min (using the standard Cockcroft-Gault formula); 4) Coagulation function: International normalized ratio (INR) ≤ 1.5 / PT ≤ 1.5 × ULN, aPTT ≤ 1.5 × ULN; if the subject is receiving anticoagulation treatment, as long as PT and INR are within the range prescribed by the anticoagulant drug, it is acceptable.

10. Estimated survival period ≥ 3 months; 11. Pregnant women should agree to use contraceptive measures (such as intrauterine device, contraceptive pills, or condoms) during the study period and within 6 months after the study; the serum HCG test should be negative within 7 days before enrollment, and must be non-lactating patients; men should agree to use contraceptive measures during the study period and within 6 months after the study.

Exclusion Criteria:

  1. Those who refuse to sign the informed consent form or refuse to undergo follow-up;
  2. Subjects who have previously or concurrently suffered from other malignant tumors;
  3. Patients who have received systemic anti-tumor treatment in the past;
  4. Those who are currently candidates for liver transplantation or have undergone liver transplantation;
  5. Those with a risk of bleeding, or coagulation dysfunction, or are undergoing thrombolytic therapy; or have experienced esophageal or gastric variceal bleeding within the past 6 months;
  6. Subjects who are known to have previously been allergic to large molecule protein preparations or the components of the applied drugs;
  7. Subjects with any active autoimmune diseases or a history of autoimmune diseases (as listed below, but not limited to: autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, pituitaryitis, vasculitis, nephritis, thyroid dysfunction (hyperthyroidism/hypothyroidism), and the use of drugs that cannot maintain thyroid function within the normal range, or previous thyroid surgery, and long-term thyroid hormone replacement therapy is required after the surgery; subjects with vitiligo or who had completely resolved asthma in childhood and do not require any intervention in adulthood can be included; subjects with asthma who require bronchodilators for medical intervention cannot be included);
  8. Subjects who are currently using immunosuppressants, or systemic, or absorbable local hormone treatments to achieve immunosuppression purposes (dose > 10mg/day prednisone or other drugs with equivalent efficacy), and are still using them within 2 weeks before enrollment;
  9. Subjects who are using traditional Chinese medicine or other immunomodulatory agents within 2 weeks before enrollment;
  10. Have poorly controlled clinical symptoms or diseases of the heart, such as: (1) NYHA grade 2 or above heart failure (2) unstable angina pectoris (3) having had a myocardial infarction within 1 year (4) having clinically significant supraventricular or ventricular arrhythmias that require treatment or intervention;
  11. Subjects with congenital or acquired immune deficiencies, such as HIV-infected individuals, or active hepatitis (transaminase does not meet the inclusion criteria, for hepatitis B: HBV DNA ≥ 2000 IU/ml or ≥ 104 copies/ml; for hepatitis C: HCV RNA ≥ 2000 IU/ml or ≥ 104 copies/ml; after nucleotide antiviral treatment, below the above standards can be included); chronic hepatitis B virus carriers, HBV DNA < 104 IU/ml, can be enrolled during the trial period if they must receive antiviral treatment simultaneously;
  12. Less than 4 weeks before the study medication, or may have received live vaccines during the study period;
  13. Subjects with known history of substance abuse of psychotropic drugs, alcoholism or drug abuse;
  14. The investigator considers it necessary to exclude from this study, for example, if the subject is judged by the investigator to have other factors that may cause the study to be prematurely terminated, such as, other serious diseases (including mental disorders) that require combined treatment, severe laboratory test abnormalities, accompanied by family or social factors that may affect the safety of the subject, or the collection of data and samples.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Receive three cycles of conversion therapy with Envafolimab combined with Suvemcitug and HAIC.

Dosage regimen:

Envafolimab: 400mg, subcutaneous injection (every 3 weeks) Suvemcitug: 2mg/kg, intravenous injection (every 3 weeks) HAIC: Based on the FOLFOX regimen, HAIC uses oxaliplatin 85mg/m² + 5-FU 2400-3200mg/m² for continuous infusion, repeated every 3 weeks

Suvemcitug is administered via intravenous infusion at a fixed dose of 2 mg/kg on Day 1 of every 21-day cycle (Q3W). Envafolimab is given by subcutaneous injection at a fixed dose of 400 mg on Day 1 of every 21-day cycle (Q3W). Concurrent Hepatic Artery Infusion Chemotherapy (HAIC) adopts standard FOLFOX regimen: Oxaliplatin 85 mg/m² administered via hepatic artery catheter, followed by continuous infusion of 5-Fluorouracil at a dose range of 2400-3200 mg/m², repeated every 3 weeks. This triple combination neoadjuvant conversion therapy will be administered for a maximum of 3 cycles to eligible patients with potentially resectable hepatocellular carcinoma (HCC) in this single-arm, single-center exploratory clinical trial.

Tumor imaging assessments will be conducted in accordance with RECIST Version 1.1 at two specified time points: baseline before treatment initiation, and within ±3 days after completion of the 3rd treatment cycle. After finishing 3 cycles of combination therapy, a mul

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Surgical conversion rate
大体时间:The conversion rate for the first to third cycles of medication (each cycle lasting 21 days)
The conversion rate for the first to third cycles of medication (each cycle lasting 21 days)

次要结果测量

结果测量
大体时间
Objective Response Rate (ORR)
大体时间:Objective response rate is defined as the proportion of patients achieving complete response (CR) or partial response (PR) assessed per RECIST v1.1. [Time Frame: During the first to third cycles of medication (each cycle lasting 21 days).]
Objective response rate is defined as the proportion of patients achieving complete response (CR) or partial response (PR) assessed per RECIST v1.1. [Time Frame: During the first to third cycles of medication (each cycle lasting 21 days).]
Major Pathological Response (MPR)
大体时间:The assessment will be conducted during the first to third cycles of medication (each cycle lasting 21 days) after the surgery.
The assessment will be conducted during the first to third cycles of medication (each cycle lasting 21 days) after the surgery.
Progression-Free Survival (PFS)
大体时间:Time from the first dose of study treatment to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first. [Time Frame: From start of treatment to disease progression or death(Each cycle lasts for 21 days.)]
Time from the first dose of study treatment to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first. [Time Frame: From start of treatment to disease progression or death(Each cycle lasts for 21 days.)]

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月31日

初级完成 (估计的)

2029年1月31日

研究完成 (估计的)

2029年7月31日

研究注册日期

首次提交

2026年7月5日

首先提交符合 QC 标准的

2026年7月27日

首次发布 (实际的)

2026年7月30日

研究记录更新

最后更新发布 (实际的)

2026年7月30日

上次提交的符合 QC 标准的更新

2026年7月27日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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