Observation Study: Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients
Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients: Safety & Efficacy Registry in Taiwan (SUPER- Taiwan)
研究概览
地位
条件
详细说明
The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence on deTACE in HCC management to physicians in the region, and to support the application of in treating advanced HCC patients.
Primary Objective:
To collect 1-year overall survival of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients in Taiwan.
Secondary Objectives:
- To evaluate the overall tumor response of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients. The tumor response is according to Modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria.
- To evaluate the local tumor response (in the tumor(s) treated with drug-eluting microsphere) by chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
- To evaluate the safety profile of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
Exploratory Objectives:
- To evaluate the downstaging and downsizing potential of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients to within Milan Criteria and to within Resection margin.
- To collect time-to-progression (TTP) and progress-free-survival (PFS) data of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
研究类型
注册 (预期的)
联系人和位置
学习地点
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Taipei、台湾、11217
- 招聘中
- Taipei Veterans General Hospital
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:Patients must meet all of the following inclusion criteria in order to be entered into the study:
- Age 20 or older.
- Patient has signed informed consent.
Patient must have a diagnosis of hepatocellular cancer confirmed by AASLD and at least one of the following method:
- Magnetic resonance imaging (MRI) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
- Contrast enhanced computed tomography (CT) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
- Histological confirmation is required for lesions with inconclusive features.
Patient must not be suitable for treatment by resection or percutaneous ablation at time of study entry.
- Patients not suitable for ablation due to lesion location may be enrolled.
- Patients with HCC recurrence but not suitable for resection or ablation maybe enrolled.
Patient MUST be with either BCLC stage B OR C, and meet the following criteria:
- Stage Child-Pugh A or B AND
- Performance status ECOG ≤ 1 WITH Vascular Invasion or WITHOUT Vascular invasion.
- Patient has a life expectancy of at least 6 months.
Exclusion Criteria:If patients meet any of the following criteria they may not be entered into the study:
- Current or previous treatment with chemo- or radiation therapy or sorafenib or drug-eluting chemoembolization (deTACE).
- Patients with concurrent cancer except non-melanomatous skin cancer.
- Female patients who are pregnant, breastfeeding, or premenopausal and not using an effective method of contraceptive.
- Performance status ECOG > 1.
- Child-Pugh Class C.
- Occlusive tumor thrombus to the main portal trunk.
- Active gastrointestinal bleeding.
- Evidence of uncorrectable bleeding diathesis.
- Extra-Hepatic spread of the HCC.
- Encephalopathy not adequately controlled medically.
- Presence of ascites not controlled medically.
- Any contraindication for MRI/ CT (eg. metallic implants).
- Allergy to contrast media that cannot be managed with prophylaxis.
- Any contraindication to arteriography.
- Any contraindication for doxorubicin administration.
- Any contraindication for hepatic embolization. Porto-systemic shunt, or an arteriovenous shunt that cannot be adequately closed prior to chemoembolization. Hepatofugal blood flow. Serum creatinine > 2mg/dL. Other condition deemed exclusionary by physician. Uncorrectable impaired clotting.
学习计划
研究是如何设计的?
设计细节
- 观测模型:仅案例
- 时间观点:预期
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Overall survival
大体时间:1 year
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To define all participants from the day of the first HepaSphere Treatment until end of study or death is reported, whichever comes first.
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1 year
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Tumor Response
大体时间:1 year
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Tumor response will be assessed using modified Response Evaluation Criteria In Solid Tumors (mRECIST) criteria to evaluate tumor necrosis under CT/ MRI and will be presented as %.
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1 year
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Adverse Event (AE)
大体时间:1 year
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Adverse event will be accessed according to CTCAE 4.0 after treatments until end of study or death.
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1 year
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Exploratory Objectives, Time-To-Progression (TTP)
大体时间:1 year
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To define all participants from the day of the first HepaSphere Treatment until tumor progression or death is first reported, whichever comes first.
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1 year
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Exploratory Objectives, Downstaging
大体时间:1 year
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Tumor staging will be accessed according to BCLC staging system and Milan criteria, and will be reviewed at follow-up until end of study or death.
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1 year
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合作者和调查者
合作者
调查人员
- 首席研究员:Yi-Hsiang Huang, M.D. Ph.D.、Taipei Veterans General Hospital, Taiwan
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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肝细胞癌的临床试验
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Taichung Veterans General Hospital完全的心脏毒性 | 非小细胞肺癌(MeSH术语:Carcinoma, Non-Small-Cell Lung) | 药物相关副作用和不良反应(MeSH术语) | 表皮生长因子受体酪氨酸激酶抑制剂台湾
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Fondazione del Piemonte per l'Oncologia招聘中乳腺癌 | 卵巢癌 | 结直肠癌 | 黑色素瘤(皮肤癌) | 非小细胞肺癌(MeSH术语:Carcinoma, Non-Small-Cell Lung)意大利