Lung Dose in Patients Treated With Yttrium-90 for Hepatocellular Carcinoma
Status: | Recruiting |
---|---|
Conditions: | Liver Cancer, Liver Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/22/2018 |
Start Date: | September 2011 |
End Date: | October 2020 |
Contact: | Alan Katz, MD |
Email: | alan_katz@urmc.rochester.edu |
Phone: | 585-273-5618 |
Analysis of Lung Dose Using Volumetric Analysis in Patients Treated With Yttrium-90 Microsphere Radioembolization for Hepatocellular Carcinoma
To Calculate the amount radiation the lung receives in patients receiving Yttrium-90 for
Liver Cancer.
Liver Cancer.
To calculate the delivered lung dose using quantitative volumetric analysis in a cohort of
patients with unresectable hepatocellular carcinoma who undergo selective internal radiation
therapy (SIRT) with Yttrium-90 glass microspheres (TheraSphere®)-and compare this analysis to
the lung dose estimated by established criteria. In addition, this study, will summarize the
pre and post-treatment clinical data to describe the URMC Y-90 experience.
patients with unresectable hepatocellular carcinoma who undergo selective internal radiation
therapy (SIRT) with Yttrium-90 glass microspheres (TheraSphere®)-and compare this analysis to
the lung dose estimated by established criteria. In addition, this study, will summarize the
pre and post-treatment clinical data to describe the URMC Y-90 experience.
Inclusion Criteria:
- Adults ≥ 18 years with no upper limit.-Receiving Y-90 Therasphere liver directed
therapy
- Pathology proven diagnosis of hepatocellular carcinoma, metastatic colon cancer or
other metastatic diseases to be treated with SIRT (Y-90)
- surgical resection not feasible at time of initiation of pre-treatment workup
-> 6 months projected life span
- ECOG 0-2
Exclusion Criteria:
- previous radioembolization of one or more liver lobes or segments without available
treatment planning and procedural documentation ie. at another facility prior to URMC
Y-90 radioembolization.
We found this trial at
1
site
Rochester, New York 14642
Principal Investigator: Alan Katz, MD
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