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临床试验/NCT01911000
NCT01911000已完成2 期

Effectiveness and Safety of the Simultaneous Radiotherapy and Hyperthermia After Transarterial Chemoembolization in Hepatocellular Carcinoma Patients Combined With Portal Vein Tumor Thrombosis: Prospective Phase II Trial

Samsung Medical Center2 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
69
试验地点
2
主要终点
Hyperthermia effect and averse event in RT for HCC with PVTT

研究概览

简要总结

The presence of portal vein tumor thrombosis (PVTT)in patients with 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, 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 option in those patients. Investigators previously reported the retrospective study that the scheduled interval TACE followed by RT for HCC combined with PVTT and 60% of the patients showed objective response without significant elevation of complication. It is reported that hyperthermia considered as the most valuable radiosensitizer in cancer treatment, theoretically. Based on those studies, we start this prospective study to evaluate the objective response and adverse event in the combination treatment of RT and hyperthermia after Transarterial chemoembolization (TACE) in the unresectable HCC patients who combined with PVTT.

详细描述

1.1 Hepatocellular carcinoma (HCC) and standard treatment HCC is the third most common cause of cancer death globally. It is also the second cause of cancer mortality in Korea, despite the incidence of HCC was fifth. The most important cause of this discrepancy is connected with the fact that the significant portion of the HCC is detected as unresectable status. At the point of HCC diagnosis, only 30% of the patients could receive standard curative treatment, like resection, liver transplantation, and radiofrequency ablation (RFA), TACE has been shown in randomized trials to improve survival compared with symptomatic therapy alone, in the patients without macrovascular involvement, extrahepatic disease and tumor related symptoms. However, in the recent review of TACE, TACE might be contraindicate or not recommended in the patients who showed vascular tumor invasion, more than 10 cm size, poor portal blood flow and/or repeated poor response.

1.2 HCC with PVTT The presence of PVTT in patients with HCC is one of the most significant prognostic factors for poor prognosis, without treatment, their survival is less than 3 months. Recently, Sorafenib, which is one of the target agents, showed survival advantage on unresectable HCC patients in two randomized study. In those study, sorafenib improved approximately three month overall survival increment, however, the median survival duration was only 10.7 months in experiment group (received sorafenib), and even 6.5 months in Asian-Pacific trial. Additionally, the possibility that sorafenib effect could be reduced in the patients had hepatitis B virus (HBV) was suggested in the subgroup analysis.

1.3 Radiation therapy (RT) for the HCC The use of RT in HCC is increased with the radiation technological advances. In the unresectable patients, RT showed 50 to 60% response rate with the dose response relationship. Especially, in the HCC patients who combined with PVTT, 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 option in those patients.

Investigators previously reported the retrospective study that the scheduled interval TACE followed by RT for HCC combined with PVTT and 60% of the patients showed objective response without significant elevation of complication.

1.4 Hyperthermia It is reported that hyperthermia is effective in S phase, Low partial oxygen pressure (pO2), acidic condition, and low perfusion site which are known as radio-resistant. Because of these characteristics, it considered as the most valuable radiosensitizer in cancer treatment, theoretically. Furthermore ,mild hyperthermia (41 to 41.5 ºC) can promote tumor reoxygenation.

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 —(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
  • Unsuitable for resection or transplant or 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

结局指标

主要结局

Hyperthermia effect and averse event in RT for HCC with PVTT

时间窗: Radiologic response and adverse event will be evaluated at 3 month after treatment.

Modified response evaluation criteria in solid tumor(mRECIST) will be used. Objective response was defined as complete and partial response. The common terminology criteria for adverse events (CTCAE version 4.0) will be used to evaluate the adverse events.

次要结局

  • To measure the time to local tumor progression(The liver CT or MRI will be examined at 3 month after treatment.)
  • Quality of life (QoL) change before and after treatment(QoL will be assessed before, 1, 3, 6 months after RT and compared each other.)
  • Hyperthermia effect on local progression free survival rate(The liver CT or MRI will be examined at 3 month after treatment and used to determine the response and presence of progression.)
  • To measure the overall survival(First follow up will be at 1 month after treatment.)
  • To validate of the prognostic index of portal vein tumor thrombosis in HCC (PITH) staging system(The liver CT or MRI will be examined at 3 month after treatment)
  • To evaluate RT response prediction probability by diffusion-weighted (DW) MRI(DW MRI will be evaluated at 1 month after treatment.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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