Stereotactic Body Radiotherapy for Liver Tumors
Completed · Not applicable
Conditions studied: Liver Metastases, Hepatocellular Carcinoma, Intrahepatic Cholangiocarcinoma
In brief
This study will evaluate the local control rate as well as acute and late toxicity rates of stereotactic body radiotherapy for the treatment of liver metastases and unresectable primary liver tumors such as hepatocellular carcinoma and intrahepatic cholangiocarcinoma.
Key facts
- Study ID
- NCT01347333
- Run by
- Mercy Research
- People needed
- 23
- Starts
- 2008-09-01
- Expected to finish
- 2016-09-01
- Last updated by the study team
- 2020-03-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient age >= 18 years
- Zubrod performance status of 0-3
- Oligometastases (1-3) with aggregate tumor diameter < 6 cm
- Metastases from neuroendocrine tumors with functional endocrine syndromes for symptom palliation
- Unresectable hepatocellular carcinoma (HCC)
- Unresectable intrahepatic cholangiocarcinoma (IHCC)
- Maximum tumor diameter < 6 cm
- Adequate liver function:
- Total bilirubin < 3 mg/dL Serum albumin > 2.5 g/dL Serum levels of liver enzymes < 3 times the upper limit of normal Normal PT and PTT unless patient is receiving anticoagulant medication
- Signed study-specific consent form
You may not qualify if…
- Maximum tumor diameter > 6 cm
- Prior radiotherapy to the liver
- Pregnant or lactating women, due to potential exposure of the fetus to RT and unknown effects of RT on lactating females
- Patients with psychiatric or addictive disorder that would preclude obtaining informed consent
Where it is running
- St. John's Mercy Medical Center — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
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