Transarterial RAdioembolization Versus ChemoEmbolization for the Treatment of HCC: A Multicenter Randomized Controlled Trial (TRACE Trial)
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 72
- 试验地点
- 1
- 主要终点
- Time to Progression (TTP).
研究概览
简要总结
Hepatocellular carcinoma (HCC) is a primary malignant tumor of the liver that accounts for an important health problem worldwide. In only 10% - 15% of all patients with HCC, tumors are considered resectable at presentation. In contrast to metastatic liver disease, there is no role for systemic chemotherapy in the treatment of HCC. Today only evidence is available for Sorafenib, a tyrosine kinase inhibiting agent. The arsenal of non-surgical therapies can roughly be divided into local ablative, transarterial and systemic therapies. In well selected patients, local ablative therapy can offer favorable long term results.
For patients with disease confined to the liver, but locally more advanced, transarterial treatment modalities are proposed. These therapies exploit the dual blood supply to the liver. HCC derives its blood supply almost entirely from the hepatic artery, while liver parenchyma derives > 75% of its blood supply from the portal vein. Antitumoral agents, such as cytotoxic drugs or radionuclides, can be delivered in close proximity of the tumor.
Examples of transarterial therapies are: transarterial chemoembolization (TACE), bland transarterial embolization (TAE), transarterial chemoembolization with drug eluting beads (TACE-DEB) and transarterial radioembolization with Iodine-131 or Yttrium-90.
TACE is currently the gold standard for treatment of patients with intermediate stage HCC, with a reported median survival of around 17 months. A novel development in the TACE treatment for HCC is the drug-eluting bead (DEB). Recently performed small clinical trials reported the efficacy of DEBs in the treatment of intermediate stage HCC, which is substantially higher compared to conventional TACE.
Yttrium-90 radioembolization (90Y-RE) is a relatively recently developed technique which implements transarterial administration of minimally embolic microspheres loaded with Yttrium-90, a β-emitting isotope, delivering selective internal radiation to the tumor.
In this study the investigators want to prospectively compare TACE-DEB and 90Y-RE, two novel treatments that both have theoretical and/or proven advantages compared to the use of conventional TACE, in patients with intermediate stage HCC.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Written informed consent.
- •The diagnosis HCC is confirmed by typical appearance on imaging or cytohistological evaluation (liver biopsy).
- •Accurate staging:
- •MRI of the liver CT-scan of the abdomen and thorax bone scintigraphy, only in case of clinical symptoms suggestive of skeletal metastases.
排除标准
- •Hypersensitivity to doxorubicin
- •Pregnancy or breastfeeding
- •Age under 18 years
- •Child-Pugh score >B7
- •ECOG performance status (PST) > 1
- •Bilirubin > 2.6 mg/dl
- •AST/ALT >5x upper limit of normal (ULN)
- •>50% of liver involvement
- •Main portal vein (right, left or common trunk) thrombosis
- •Extra-hepatic disease
- •Previous treatment of study target lesions
- •99mTc-labelled macroaggregated albumin (99mTc-MAA) scintigraphy shows lack of MAA uptake in tumor (photopenic lesion)
- •Activity > 610 MBq and activity reduction would imply a liver target dose > 80 Gy
- •patients who are declared incompetent or suffering from physic disorders that make a comprehensive judgement impossible, such as psychosis.
- •Unmanageable intolerance for contrast medium
- •Life expectancy < 3 months or otherwise impossible follow-up
- •Inadequate bone marrow, liver and/or renal function
- •other contraindications to hepatic embolization procedures.
研究组 & 干预措施
Yttrium-90 radioembolization (90Y-RE)
干预措施: 90Y-RE (Drug)
Transarterial chemoembolization with drug eluting beads
Transarterial chemoembolization is performed with drug eluting beads, polyvinyl alcohol-based microspheres (DC Beads, Biocompatibles) loaded with the chemotherapeutic agent doxorubicin.
干预措施: TACE-DEB (Drug)
结局指标
主要结局
Time to Progression (TTP).
时间窗: Patients will be followed over a 2 years period.
Tumor progression is defined according to the modified Response Evaluation Criteria in Solid Tumors (mRECIST) response evaluation criteria. The mRECIST evaluation criteria define progressive disease by the implication of target lesions response, non-target lesions response and the occurrence of new lesions.
次要结局
- Time to Local Progression (TLP).(Since start of treatment untill local tumor progression with a maximum of 2 years follow up.)
- Survival of patients dedicated to either treatment arm.(Patients are followed for up to 2 years.)
- Quality of life EQ5D(Before treatment and after treatment on a 3 monthly interval during 2 years.)
- Tumor response to therapy according to mRECIST criteria(Before treatment and after treatment on a 3 monthly interval during 2 years.)
- Treatment-related costs.(After follow up of 2 year.)
- Toxicities and adverse events (recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE version 3.0)(6 months following last treatment)