About this trial
Standard planning constraints for liver SBRT incorporate strict dose-volume limits for normal liver parenchyma to minimize the risk of radiation-induced liver disease. The presence of diurnal and fasting/fed variations in liver volume therefore carry substantial potential for introducing errors into estimates of dose-volume distribution within normal liver tissue, as well as affecting day-to-day setup fidelity and organ alignment for treatment. This prospective study will examine how diurnal and fast-fed variations in liver volume affect treatment planning for abdominal SBRT.
Eligibility criteria
Qualifiers
None
Disqualifiers
Had prior Radiation Therapy to the liver
Contraindication to receipt of iodinated IV contrast for CT (such as renal insufficiency or allergy that cannot be overcome by premedication)
Pregnancy/lactation OR woman of childbearing potential who is unable or unwilling to use adequate contraception during Radiation Therapy.
Inability to fast.
Trial design
Treatments tested in this trial
- Standardized high-carbohydrate meal
Treatment groups
Sponsors and collaborators
University of Pittsburgh
Lead sponsor
American College of Radiation Oncology
Collaborator