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Use of TheraSphere® Yttrium-90 Glass Microspheres for Primary and Metastatic Liver Tumors
This study is currently recruiting participants.
Study NCT00493883   Information provided by Southwestern Regional Medical Center
First Received: June 26, 2007   Last Updated: April 22, 2009   History of Changes
This Tabular View shows the required WHO registration data elements as marked by

June 26, 2007
April 22, 2009
December 2006
  • 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 ] [ Designated as safety issue: No ]
  • Toxicity, which may include radiation induced liver damage, pain, consequences of shunting, toxic deaths. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
  • Survival time [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00493883 on ClinicalTrials.gov Archive Site
 
 
 
Use of TheraSphere® Yttrium-90 Glass Microspheres for Primary and Metastatic Liver Tumors
Use of TheraSphere® Yttrium-90 Glass Microspheres for Primary and Metastatic Liver Tumors

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.
Phase I, Phase II
Interventional
Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
  • Carcinoma, Hepatocellular
  • Liver Neoplasms
Device: yttrium Y 90 microspheres (TheraSphere®)
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
50
December 2010
December 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Age >= 18.
  2. Cancer visible in liver on CT,MR,US or PET scan.
  3. Primary cancer in the liver (hepatocellular carcinoma), or metastatic cancer involving the liver from a primary such as but not limited to lung, breast, colon, upper GI, neuroendocrine, melanoma.
  4. Life expectancy greater than 2 months
  5. Performance status of ECOG 2 or better (Ambulatory and capable of all selfcare, but unable to carry out any work activities. Up and about more than 50% of waking hours.)
  6. Patients have tried and/or are aware of all FDA approved therapies for their condition.

Exclusion Criteria:

  1. Vascular shunt that cannot be corrected.
  2. Bulky cancer outside of liver. Active cancer within the liver should be a greater volume than the active cancer outside the liver / in the remainder of body.
  3. Pregnancy
  4. Hematologic primary such as lymphoma, leukemia, myeloma.
  5. Body weight 300 lbs. and above
  6. Evidence of portal hypertension, splenomegaly or ascites.
Both
18 Years and older
No
Contact: Michele M Sumner, BS, CCRC 1-877-896-3698
Contact: Sharrese Bishop, BSN, CCRC 1-877-896-3698
United States
 
 
NCT00493883
Douglas A. Kelly, M.D., Southwestern Regional Medical Center
 
Southwestern Regional Medical Center
 
Principal Investigator: Douglas A. Kelly, M.D. Cancer Treatment Centers of America at Southwestern Regional Medical Center
Southwestern Regional Medical Center
April 2009

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.