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临床试验/NCT02582034
NCT02582034已完成2 期

Selective Internal Radiation Therapy for Hepatocellular Carcinomas With Yttrium-90 Loaded Microspheres: Optimized Dosimetry Versus Standard Dosimetry

Center Eugene Marquis4 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2015年12月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
56
试验地点
4
主要终点
The primary endpoint is to compare the response rate of the treated lesion at the first radioembolization, evaluated using European Association for the Study of the Liver (EASL) criteria of yttrium-90 marked glass microspheres SIRT

研究概览

简要总结

The purpose of this study is to determine whether a treatment with Therasphere which is optimized is more efficient compared to a standard treatment for patients suffering from hepatocellular carcinomas.

详细描述

For patients suffering from hepatocellular carcinoma, a palliative treatment can be proposed if tumor expansion is limited to the liver. One of palliative treatment is the the Selective Internal Radiation Therapy (SIRT) with Therasphere®. This treatment is made secure by performing a diagnostic angiogram coupled with a hepatic perfusion scintigraph with which patients at risk of complications are identified and excluded. The treatment objective, with the standard dosimetric approach, is to deliver an absorbed dose of 120 ± 20 Gy to the treated hepatic volume, most often one lobe. Recent retrospective trials show that an optimized dosimetric approach, considering the dose absorbed by the tumor, is technically achievable and would probably make it possible to obtain a better effectiveness. In our experience, treatment personalisation have been described to be used for 60% of the patients with a tumor larger than 7 cm underlying the clinical impact of this new approach.

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

性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 18,
  • •Written free and informed consent,
  • •Histologically demonstrated Hepatocellular Carcinoma (HCC), not a candidate for surgery or local ablative treatment (radio frequency, etc.)
  • •Barcelona Clinic Liver Cancer (BCLC) classification A, B or C,
  • •At least one lesion ≥ 7 cm,
  • •Hepatic reserve (hepatic parenchyma not treated) after the first SIRT ≥ 30%,
  • •Unilateral involvement, minimal bilateral involvement allowed only with a hepatic reserve ≥ 30% after SIRT
  • •Child A classification only, or B but with bilirubinemia <35 micromol/L,
  • •Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1,
  • •Patients whose biological parameters meet the following criteria:
  • •Hemoglobin ≥ 8.5 g/dL,
  • •Granulocytes ≥ 1500/mm3,
  • •Platelets ≥ 50,000/mm3,
  • •Bilirubinemia <35 micromol per liter,
  • •Transaminases ≤ five times the upper limit of normal,
  • •Creatininemia ≤ 1.5 times the normal upper limit,
  • •Expected survival over 12 weeks,
  • •Negative pregnancy test for women of childbearing age,
  • •If sorafenib has been taken the diagnostic angiogram must follow it by at least four weeks after its stop.

排除标准

  • •HCC operable or accessible to a local ablative treatment (radio frequency),
  • •Hepatectomy history unless a segmental treatment is considered, with a hepatic reserve ≥ 30% after SIRT,
  • •Prior treatment with sorafenib unless stopped at least four weeks earlier,
  • •History of chemo-embolization of the principal lesion, except in case of nodular residual lesion measuring at least 7 cm or in case of progression after initial response,
  • •Bilateral disease requiring a whole liver injection or with a hepatic reserve < 30% after SIRT
  • •Treatment of another cancer less than one year earlier,
  • •Extra-hepatic metastases other than adenopathies of the hilum smaller than 2 cm,
  • •>70% tumor invasion of the liver,
  • •Bilirubinemia ≥ 35 µmol/L,
  • •A Severe underlying biliary pathology:
  • •Bile duct anomaly (stent, dilation) Cirrhosis of biliary origin,
  • •Women of childbearing age without contraception
  • •Pregnant or nursing women

研究组 & 干预措施

Standard dosimetry

Active Comparator

Standard Internal Radiation Therapy : Dose of radiation delivered to the tumoral volume is fixed : 120 Gray (GY)

干预措施: Standard Internal Radiation Therapy (Radiation)

Optimized dosimetry

Experimental

Optimized Internal Radiation Therapy : Dose of radiation absorbed by the tumor is > 205 GY, if possible 250 or 300 Gy.

干预措施: Optimized Internal Radiation Therapy (Radiation)

结局指标

主要结局

The primary endpoint is to compare the response rate of the treated lesion at the first radioembolization, evaluated using European Association for the Study of the Liver (EASL) criteria of yttrium-90 marked glass microspheres SIRT

时间窗: 3 months after treatment administration

次要结局

  • Progression Free Survival(Up to 12 months)
  • Overall survival(Up to 30 months after inclusion of the 1st patient)
  • Related Adverse Events in both arms as assessed by National Cancer Institute criteria (National Cancer Institute Common Terminology Criteria for Adverse Events, (NCI CTCAE) version 4).(Up to 12 months)
  • Progression free survival not accessible to SIRT(Up to 12 months after treatment administration)
  • Post-therapeutic dosimetry measured by Positron emission tomography-computed tomography PET / CT(Day one of treatment administration)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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