跳至主要内容
临床试验/NCT02290977
NCT02290977Unknown2 期

Scheduled Interval Trans-catheter Arterial Chemo-embolization and Radiation Therapy for Hepatocellular Carcinoma Combined With Portal Vein Tumor Thrombosis: Prospective Phase II Trial

Samsung Medical Center2 个研究点 分布在 2 个国家目标入组 40 人开始时间: 2014年11月最近更新:
适应症
干预措施

试验速览

阶段
2 期
入组人数
40
试验地点
2
主要终点
Overall survival rate after scheduled TACE-RT for HCC with PVTT

研究概览

简要总结

The presence of portal vein tumor thrombosis (PVTT) in patients with hepatocellular carcinoma (HCC) is one of the most significant prognostic factors for poor prognosis, without treatment, their survival is less than 3 months. In the HCC patients who combined with PVTT, Radiation therapy (RT) showed 50% of local control and about 10 months survival duration. Despite the standard treatment of the HCC combined with PVTT is sorafenib, but Korean Liver Cancer Study Group (KLCSG) recommend RT as an alternative option in those patients. Investigators previously reported the retrospective study that the scheduled interval Trans-catheter Arterial Chemo-embolization (TACE) followed by RT for HCC combined with PVTT and 60% of the patients showed objective response without significant elevation of complication. However, the prospective outcomes of TACE followed by RT for HCC are scantly reported. Based on those background, we start this prospective study to evaluate the clinical outcomes and adverse event in the RT after TACE in the unresectable HCC patients who combined with PVTT.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have a diagnosis of HCC by at least one criterion listed below (korean liver cancer study group (KLCSG) guideline 2009) 1.1 Pathologically (histologically or cytologically) proven diagnosis of HCC 1.2 Liver nodule in high risk group 1.2.1 If alpha fetoprotein (AFP) ≥200 ng/mL , ≥ 1 typical HCC enhancing pattern on dynamic contrast enhanced CT or MRI 1.2.2 If AFP<200 ng/mL, ≥2 typical HCC enhancing pattern on dynamic contrast enhanced CT, MRI, and angiography 1.3 ≥ 2 cm nodule in liver cirrhosis (LC), ≥ 1 typical HCC enhancing pattern on dynamic contrast enhanced CT or MRI
  • Patients must have a diagnosis of PVTT 2.1 Early arterial enhancement and delayed washout on multiphasic CT or MRI
  • Eastern cooperative oncology group performance status 0 1 2
  • Age ≥ 20 and 70 or less
  • Unsuitable for resection or transplant or radiofrequency ablation (RFA)
  • Unsuitable for or refractory to TACE or drug eluting beads (DEB)
  • Agreement of study-specific informed consent
  • Assessment by radiation oncologist and medical oncologist or hepatologist within 28 days prior to study entry?
  • Child-Pugh score A-B within 7 days prior to study entry
  • Normal liver (Liver minus gross tumor volume) ≥ 700 cc
  • Blood work requirements
  • Absolute neutrophil count (ANC) ≥ 1,500 /mm3, Platelet ≥ 70,000/mm3, Hgb ≥ 8 g/dl
  • Liver function test (LFT): Total bilirubin<3.0 mg/dL, International normalized ratio(INR) < 1.7, Albumin ≥ 2.8g/dL, Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT)< 6 X normal
  • Serum creatinine < 1.5 X normal, or creatinine clearance ≥ 60 mL/min
  • Male, consent contraception at least 6 months
  • Childbearing potential woman, consent contraception at least 6 months
  • Life expectancy more than 12 weeks
  • Stable breathing more than 5 minutes

排除标准

  • Complete obstruction of main portal vein
  • Pregnant and/or breastfeeding woman
  • Previous upper abdominal RT history
  • Uncontrolled active co-morbidity
  • Another primary cancer history within 2 years
  • Uncontrolled ascites or hepatic encephalopathy
  • Connective tissue disease which known as radiation hypersensitivity
  • Uncontrolled moderate to severe gastroduodenal ulcer or esophagogastric varices

研究组 & 干预措施

Scheduled TACE-RT

Experimental

RT will be delivered at two weeks after TACE for HCC combined PVTT.

干预措施: Scheduled interval TACE - RT (Radiation)

结局指标

主要结局

Overall survival rate after scheduled TACE-RT for HCC with PVTT

时间窗: One year after treatment

Overall survival rate will be evaluated at 1 year after treatment.

Adverse event assessed using Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 after scheduled TACE-RT for HCC with PVTT

时间窗: Three months after treatment

Adverse event will be evaluated at 3 months after treatment.

次要结局

  • Radiologic response assessed by modified Response Evaluation Criteria for Solid Tumors (mRECIST) after scheduled TACE-RT for HCC with PVTT(Three months after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paik Yong Han

Associate Professor

Samsung Medical Center

研究点 (2)

Loading locations...

相似试验