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临床试验/JPRN-jRCTs031230128
JPRN-jRCTs031230128招募中2 期

envatinib plus cisplatin hepatic arterial infusion chemotherapy for borderline resectable hepatocellular carcinoma: A Multicenter Phase II Study - LEOPARD-Neo

Ikeda Masafumi0 个研究点目标入组 24 人开始时间: 2023年6月9日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 < 80age old(—)
性别
All

入选标准

  • 1) Histologically or clinically confirmed hepatocellular carcinoma (except for mixed type).
  • 2) Presence of vascular invasion. (Vascular invasion refers to portal vein tumor thrombosis, hepatic vein tumor thrombus, and bile duct tumor thrombus.)
  • 3) Technically resectable HCC
  • 4) Age >=18 years and <80 years.
  • 5) No prior systemic therapy of primary lesion (Prior treatment history (Local therapy such as hepatectomy, RFA, TACE) is not a consideration.
  • 6) Having measurable lesions
  • 7) ECOG Performance Status 0 or 1.
  • 8) Sufficient organ functions
  • Bone marrow
  • Neutro>= 1,500 /mm3
  • Hb>= 8.5 g/dL
  • PLT>= 75,000 /mm3
  • T-Bil<= 2.0 mg/dL
  • ALB>= 2.8 g/dL
  • AST<=105 IU/L
  • ALT Male <=210 IU/L Female <=115IU/L
  • Amylase<= 264U/L
  • KidneyCr <= 1.2 mg/dL
  • Creatinine Clearance >= 50 ml/min
  • Coagulation
  • International normalized ratio (PT-INR)<= 2.3
  • 9) Child-Pugh score 5-6 points.
  • 10) Controllable blood pressure by the use of antihypertensive agents with no more than three drugs
  • 11) Procedural cisplatin hepatic arterial infusion chemotherapy is expected to be feasible.
  • 12) Written informed consent has been obtained from the patient.

排除标准

  • 1) Extrahepatic metastases.
  • 2) Previously treated with lenvatinib or cisplatin for hepatocellular carcinoma.
  • 3) Moderate or greater ascites or pleural effusion unresponsive to treatment.
  • 4) When the proteinuria is 2+ or more in the urinary protein qualitative test, 24-hour urine collection is carried out, and the urinary protein is recognized over 1 g/24 hour. (However, substitution by urinary protein/creatinine ratio is allowed.)
  • 5) Hepatic encephalopathy
  • 6) The following serious complications
  • Uncontrolled hypertension despite treatment (diastolic pressure exceeds 100 mmHg)
  • Difficult-to-control heart failure despite treatment; angina; arrhythmias
  • Poorly controlled diabetes despite treatment
  • Myocardial infarction within 6 months of onset
  • Active double cancers (synchronous double cancers, metachronous double cancers within 3 years of disease-free interval)
  • Serious psychiatric disorder
  • History of hypersensitivity to iodine-containing drugs or contrast media.
  • Serious drug allergy
  • 7) Bleeding or thrombotic disease or a history of gastrointestinal bleeding or active hemoptysis within 28 days before enrollment.
  • 8) Pregnant, breastfeeding, or possibly or intentionally pregnant, or wish to raise a child.
  • 9) Difficult oral intake.
  • 10) HIV positive.
  • 11) Complicated by active infection requiring treatment (except for hepatitis virus).
  • 12) Complicated by pulmonary fibrosis or interstitial pneumonia.
  • 13) Treatment for blood conditions (including blood transfusions, blood products or hematopoietic factors products such as Granulocyte-Colony Stimulating Factor: G-CSF) in the 14 days prior to enrollment.
  • 14) The investigator judges it inappropriate to conduct the study safely.

研究者

发起方
Ikeda Masafumi

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