A Pilot Study to assess Theragnostically Planned Liver Radiation with Functional DVH Analysis to Optimize Individualized Radiation Therapy

R
Ryan Rhome, MD

Primary Investigator

Overview

The purpose of this study is to compare radiation treatment plans that are designed for patients with liver cancer.

Description

One treatment plan will be created using routine procedures and scans normally performed for radiation treatment planning. The other treatment plan will be created using routine procedures with the addition of two imaging scans; a HIDA (Hepatobiliary Iminodiacetic Acid) scan and an MRI (Magnetic Resonance Imaging) scan. This study will evaluate if adding these imaging scans to treatment planning can reduce the amount of radiation to healthy liver tissue during treatment.

Eligibility

You may be eligible for this study if you meet the following criteria:

  • Conditions:
    liver cancer,Hepatocellular Carcinoma,Cholangiocarcinoma
  • Age: Between 18 Years - 100 Years
  • Gender: All

Inclusion Criteria
Primary liver malignancy including hepatocellular carcinoma (HCC) or cholangiocarcinoma
Subjects must have a Child-Turcotte-Pugh (CTP) score less than or equal to 7
Exclusion Criteria
Subject who are pregnant or planning to become pregnant during the study
No more than 3 lesions can be treated. Total diameter of all lesions must be less than or equal to 6 cm
Prior radiation treatment to the upper abdomen
Active infection, active upper GI ulceration or hemorrhage, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia


Additional Information:

Updated on 09 Mar 2024. Study ID: 1701880309 (IUSCC-0604)

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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