Liver Volume Variation Effect on SBRT Planning and Delivery for Upper Abdominal Malignancies

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Pittsburgh

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

17 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Pittsburgh

Lead sponsor

American College of Radiation Oncology

Collaborator