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Clinical Trial Summary

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.


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02582034
Study type Interventional
Source Center Eugene Marquis
Contact
Status Completed
Phase Phase 2
Start date December 2015
Completion date December 2018

See also
  Status Clinical Trial Phase
Completed NCT01306058 - Sorafenib and TRC105 in Hepatocellular Cancer Phase 1/Phase 2