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The DoHAICs Study Expansion Phase

Clinical Study on the Efficacy and Safety of Donafenib Combined With Hepatic Artery Infusion Chemotherapy and Sintilimab as the First-line Treatment for Unresectable Hepatocellular Carcinoma - the DoHAICs Study Expansion Phase

We explored the efficacy and safety of the first-line treatment of unresectable hepatocellular carcinoma with donafenib combined with hepatic artery infusion chemotherapy (HAIC) and sintilimab .

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

90

段階

  • フェーズ2

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Voluntarily participate in the trial and provide written informed consent.
  • Age between 18 and 80 years (inclusive), regardless of gender.
  • Patients with hepatocellular carcinoma (HCC) clinically diagnosed per the "Standard for Diagnosis and Treatment of Primary Liver Cancer (2024 Edition)" or confirmed by histology/cytology.
  • Patients with inoperable or metastatic hepatocellular carcinoma.
  • No prior systemic therapy for advanced disease. Patients who received adjuvant chemotherapy following local therapy are eligible if chemotherapy was completed >12 months ago and disease progression or metastasis has occurred.
  • Completion of the last interventional therapy, radiotherapy, or ablation therapy >4 weeks prior.
  • For patients with prior hepatectomy, resection must have been R0, and tumor recurrence must have occurred more than 24 months after surgery.
  • At least one measurable lesion as defined by RECIST 1.1 criteria.
  • Life expectancy ≥3 months.
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.
  • Child-Pugh score ≤7.
  • Able and willing to comply with the protocol for the observation of adverse events and efficacy.
  • Adequate organ function, defined as meeting the following criteria:
  • Hematological function (without transfusion or granulocyte colony-stimulating factor [G-CSF] support within 14 days prior to screening):
  • Hemoglobin ≥90 g/L.
  • Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L.
  • Platelet count ≥75 × 10⁹/L.
  • Biochemical tests (without albumin infusion within 14 days prior to screening):
  • Albumin ≥28 g/L.
  • Total bilirubin ≤2 × upper limit of normal (ULN).
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤5 × ULN.
  • Alkaline phosphatase (ALP) ≤5 × ULN.
  • Serum creatinine ≤1.5 × ULN.
  • Coagulation function:
  • International normalized ratio (INR) or prothrombin time (PT) ≤1.5 × ULN.
  • Activated partial thromboplastin time (APTT) ≤1.5 × ULN.

Exclusion Criteria:

  • Histologically/cytologically confirmed components such as fibrolamellar hepatocellular carcinoma, sarcomatoid hepatocellular carcinoma, or cholangiocarcinoma.
  • History of malignancies other than hepatocellular carcinoma, except under the following circumstances:
  • The patient has undergone potentially curative treatment with no evidence of that disease for 5 years.
  • Successfully resected basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the cervix, or other carcinoma in situ.
  • Diffuse tumor lesions.
  • History of hepatic encephalopathy, hepatorenal syndrome, or liver transplantation.
  • Clinically symptomatic pleural effusion, ascites, or pericardial effusion requiring drainage.
  • Central nervous system metastases.
  • History of severe psychiatric illness.
  • Diseases affecting the absorption, distribution, metabolism, or excretion of the investigational drug (e.g., severe vomiting, chronic diarrhea, intestinal obstruction, malabsorption, etc.).
  • Prior allogeneic stem cell or solid organ transplantation.
  • Prior treatment with anti-VEGF/VEGFR, RAF, MEK pathway targeted therapies (e.g., sorafenib, lenvatinib, regorafenib) or immunomodulators (e.g., anti-PD-1, anti-PD-L1, anti-CTLA-4 antibodies).
  • Prior other systemic anti-tumor therapy, including Chinese herbal medicine with anti-tumor indications, completed less than 2 weeks before study drug initiation; or patients with adverse events from prior therapy not recovered to ≤ Grade 1 per CTCAE (excluding alopecia and Grade 1/2 neuropathy caused by oxaliplatin).
  • Concurrent use of medications known to prolong QTc interval and/or induce Torsades de Pointes (TdP), or medications that affect drug metabolism.
  • Past or present congenital or acquired immunodeficiency diseases.
  • Active or history of autoimmune or inflammatory diseases (including but not limited to: autoimmune hepatitis, interstitial pneumonia, inflammatory bowel disease, systemic lupus erythematosus, vasculitis, uveitis, hypophysitis, hyper- or hypothyroidism, asthma requiring bronchodilators, etc.). Patients with vitiligo or asthma that was fully resolved in childhood and requires no intervention in adulthood may be included.
  • Use of systemic immunosuppressive medication within 2 weeks prior to enrollment, or anticipated requirement for such medication during the study, except for:
  • Intranasal, inhaled, topical, or local corticosteroid injections (e.g., intra-articular).
  • Systemic corticosteroids at physiological doses not exceeding 10 mg/day prednisone or equivalent.
  • Prophylactic use of corticosteroids for hypersensitivity reactions.
  • Known or suspected hypersensitivity to donafenib, drugs of the same class, or history of hypersensitivity to chimeric or humanized antibodies or fusion proteins, or allergy to any excipient of the investigational drug.
  • Active bleeding or coagulation disorders, bleeding tendency, or undergoing thrombolytic, anticoagulant, or antiplatelet therapy.
  • Thrombotic or thromboembolic events within the past 6 months, such as stroke and/or transient ischemic attack, deep vein thrombosis, pulmonary embolism, etc.
  • History of esophageal or gastric variceal bleeding due to portal hypertension within the past 6 months, or any life-threatening bleeding event within the past 3 months.
  • Significant cardiovascular disease, including but not limited to: acute myocardial infarction, severe/unstable angina, or coronary artery bypass grafting within the past 6 months; congestive heart failure (NYHA class >2); poorly controlled arrhythmias requiring pacemaker treatment; uncontrolled hypertension (systolic BP ≥140 mmHg and/or diastolic BP ≥90 mmHg).
  • Other clinically significant abnormalities, deemed by the investigator to affect safety evaluation, such as uncontrolled diabetes, chronic kidney disease, Grade II or higher peripheral neuropathy (CTCAE v6.0), abnormal thyroid function, etc.
  • Active or poorly controlled severe infection; active infections including:
  • Positive for Human Immunodeficiency Virus (HIV) (HIV1/2 antibodies).
  • Active Hepatitis B (HBsAg positive or HBV DNA >2000 IU/mL with abnormal liver function).
  • Active Hepatitis C (HCV antibody positive or HCV RNA ≥10³ copies/mL with abnormal liver function).
  • Active tuberculosis.
  • Other uncontrolled active infections (CTCAE v6.0 > Grade 2).
  • Incomplete recovery from surgery, such as unhealed wounds or severe postoperative complications.
  • Pregnancy, lactation, or patients of childbearing potential unwilling or unable to use effective contraception.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Donafenib combined with hepatic artery infusion chemotherapy and sintilimab
Donafenib combined with hepatic artery infusion chemotherapy and sintilimab injection as the first-line treatment for unresectable hepatocellular carcinoma
Donafenib (200 mg twice daily, taken orally, initiated 3-7 days before the first HAIC session)
sintilimab (200 mg intravenously every 3 weeks, administered 0-1 day before each HAIC treatment)
HAIC (oxaliplatin 85 mg/m2 over 2 hours, leucovorin 400 mg/m2 over 2 hours, bolus fluorouracil 400 mg/m2 within the first 10 minutes, followed by fluorouracil infusion 1200 mg/m2 over 23 hours, every 3 weeks.)

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
event-free survival
時間枠:The time from enrollment to the date of first documented progression, recurrence, or death from any cause, whichever came first, assessed up to 36 months
The time from enrollment to the date of first documented progression, recurrence, or death from any cause, whichever came first, assessed up to 36 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年5月20日

一次修了 (推定)

2027年6月1日

研究の完了 (推定)

2027年6月1日

試験登録日

最初に提出

2025年12月22日

QC基準を満たした最初の提出物

2026年5月7日

最初の投稿 (実際)

2026年5月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月13日

QC基準を満たした最後の更新が送信されました

2026年5月7日

最終確認日

2025年12月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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