The purpose of this study is to provide supervised access to treatment with TheraSphere® to eligible patients with primary and metastatic cancer and evaluate response to treatment, survival and toxicity. The study has the following objectives: * Provide supervised access to treatment with TheraSphere to eligible patients with primary and metastatic cancer to the liver. * Evaluate patient experience and toxicities associated with TheraSphere treatment * Evaluate predisposing factors that may influence results and toxicity
This study will use angiographic administration of radioactive TheraSphere® Yttirum-90 microspheres into the hepatic artery, to treat 50 patients with primary or secondary cancer involving the liver. The study population are those who have failed standard therapies, have a majority of their cancer in the liver, have a good performance status and reasonable hepatic function. Outcomes being studied are response to treatment, survival and toxicity. 1. Range of patients who can be offered TheraSphere® 2. Tumor response rates, in terms of size, volume, contrast enhancement and PET avidity 3. Survival time 4. Determine response in relation to histology and other parameters 5. Ability to tolerate repeat treatments 6. Toxicity, which may include radiation induced liver damage, pain, consequences of shunting, toxic deaths.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
81
Y-90 is incorporated into very tiny glass beads, it can be injected into the liver through the blood vessels supplying the liver
Cancer Treatment Centers of America at Southwestern Regional Medical Center
Tulsa, Oklahoma, United States
Tumor response rates, in terms of size, volume, contrast enhancement and PET avidity
Time frame: 2 to 3 months after treatment(s) up to 2 years
Toxicity, which may include radiation induced liver damage, pain, consequences of shunting, toxic deaths.
Time frame: 2 years
Survival time
Time frame: 2 years
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