LAVI Ltd
July 2010

1. In a phase III study trial reported on June 21st in the Journal of Clinical Oncology,46 patients were  
   enrolled in a randomized study to protracted fluorouracil infusion on days 1 through 14 every 3 weeks
   with or without hepatic intra-arterial injection of SIR-Spheres®. With a median follow-up of 2 years the
   results are as follows:

   • The median time to liver progression was 5.5 months compared to 2.1 months  
      in the control group.
   • The toxicity rate was lower in the study group, compared to the control group.
   • Median overall survival was 10.0 months in the study group compared to 7.3 
     months in the control group.


2. SIR-Spheres® is registered in the Ministry Of Health (M.O.H) as a medical 
   device. The current license includes the USA + EU + Australian indications. This
   means that the SIR-Spheres® may be injected to 
   patients suffering from unresectable malignant tumors in the liver, either primary
   tumors such as Hepatoma or metastatic tumors from any origin.



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