Assessment of Response of Unresectable Hepatocellular Carcinoma to Combination Chemoembolization and Stereotactic Body Radiation Therapy
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Number of Participants With Objective Response Rate
研究概览
简要总结
The purpose of this study is to develop better ways to treat liver cancer, known as hepatocellular carcinoma or HCC, while it is still in the liver. Many treatments exist to treat tumors in the liver when they are small but after they grow past a certain size, local therapies such as surgery, Trans-Arterial Chemo Embolization (TACE), or Radiofrequency Ablation (RFA) are not effective. The purpose of this study to test the combination of two known treatments - TACE and Stereotactic Body Radiation Therapy (SBRT) - to be used together to treat larger or difficult to access liver tumors. Each treatment has been shown to work well but has limitations. The study will combine the treatments in an organized sequence and monitor closely how effective this combination controls tumors.
详细描述
Hepatocellular carcinoma (HCC) is the third ranked cause of global cancer mortality. There is an increasing incidence of HCC in the United States over the last twenty years, largely due to the Hepatitis C epidemic but increasingly related as well to nonalcoholic fatty liver disease.
This is a non-randomized pilot study to assess the objective response rate and durability of response of combination Trans-Arterial Chemoembolization (TACE) with immediate stereotactic body radiation therapy (SBRT) in the treatment of unresectable hepatocellular carcinoma (HCC). Eligible patients will be selected based on having a lesion greater than 3 cm which would make them ineligible for other local therapies such as TACE and thermal ablation (TA). Eligible, consented, and registered patients will be treated with two sessions of standard TACE with ethiodol separated by a 4-week interval. After ensuring adequate return to baseline liver function, the patients will then be treated with SBRT to the targeted lesion to 30-45 Gy in 5 fractions. Tumor response will be assessed using mRECIST criteria as well diffusion weight imaging (DWI) via Magnetic Resonance Imaging (MRI) surveillance. In addition, tolerability and toxicity will be recorded via CTCAE v. 4.0. The essential hypothesis of this study is that combination TACE and SBRT for > 3 cm HCC will produce higher response rates and durable control compared to TACE alone.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participants must be diagnosed with HCC either pathologically or by the American Association for the Study of Liver Diseases (AASLD) radiographic criteria (Bruix Hepatology 2011). The criteria specifies CT or MRI intense arterial uptake followed by "washout" of contrast in the venous-delayed phases. Any atypical lesions must be confirmed by biopsy.
- •A single liver lesion with tumor size ≥ 3 cm as defined as maximal diameter in the axial dimension on MRI. Included in the measurement are both enhancing and non-enhancing components of the lesion.
- •Maximum tumor size of 7 cm as defined as maximal diameter in the axial dimension on MRI.
- •Age ≥ 18 years
- •Child-Pugh class A or B7 without ascites
- •ECOG score 0
- •No prior treatment of current HCC. However, recurrent HCC after resection may be included.
- •Ability to understand and the willingness to sign a written informed consent document.
排除标准
- •Pregnancy which will be assessed via pregnancy test prior to TACE and repeated prior to SBRT.
- •Metastatic disease outside of the liver
- •Vascular invasion as evidenced by vessel occlusion or radiographic evidence of tumor thrombus.
- •Contraindications to MRI, including claustrophobia, metallic implants, and pacemakers
- •Tumor for which adequate radiation dosage cannot be safely delivered (see dose constraints below)
- •Prior therapeutic radiation therapy to the abdomen and/or lower thorax as defined as below the carina to the pelvic inlet.
- •Inability to provide informed consent based on persistent lack of understanding, inability to find adequate translation, impaired mental status such as mental retardation, drug induced, or traumatic brain injury.
- •Multiple liver tumors making the patient a BCLC Stage B
- •Prior treatment, except for surgical resection, to the lesion being targeted in the protocol.
研究组 & 干预措施
Participants with HCC
Participants with HCC with a lesion greater than 3 cm treated with TACE/SBRT combination
干预措施: SBRT (Radiation)
Participants with HCC
Participants with HCC with a lesion greater than 3 cm treated with TACE/SBRT combination
干预措施: TACE (Drug)
结局指标
主要结局
Number of Participants With Objective Response Rate
时间窗: up to 72 months
Tumor response will be assessed using mRECIST criteria as well diffusion weight imaging (DWI) via Magnetic Resonance Imaging (MRI) surveillance. * Complete response (CR): Disappearance of all target lesions * Partial response (PR): At least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD * Stable disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum LD since the treatment started * Progressive disease (PD): At least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions
次要结局
- Time to CR(up to 72 months)
- Time to Progression (TTP)(up to 80 months)
- Number of Participants With Overall Survival (OS)(2 years)
- Progression Free Survival (PFS)(up to 72 months)
- Change in Child-Turcotte-Pugh (CTP) Score(3 months)
研究者
Michael Buckstein
Assistant Professor
Icahn School of Medicine at Mount Sinai