liver cancer
Conditions
Interventions
None listed
Sponsors
Academisch Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patients with hepatocellular carcinoma or liver metastases of other primary who are referred for SIRT. Age * 18 years. Signed informed consent obtained prior to any study-specific procedure.
Exclusion criteria
Exclusion criteria: Age * 18 years. Pregnancy or breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of this study is defined as segmental liver function in treated and untreated lobes expressed as absolute value (%/min/m2) and percentage of total liver function 6 weeks after SIRT; and changes in total liver function after SIRT. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoint is the correlation of scintigraphic findings with clinical and biochemical parameters such as performance score, Chil-Pugh-Turcotte score and serologic liver function tests collected as part of the routine patient management. | — |
Countries
Netherlands
Outcome results
None listed