Expired Study
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Dallas, Texas 75390


Purpose:

Patients that have had staging studies identifying them as AJCC stage IV with up to five liver metastases will be considered for the study. About 60 patients will take part in this study at UT southwestern, Parkland Health & Hospital System, and Methodist Richardson Cancer Center. There are four dose cohorts for this study and each cohort will enroll a minimum of 7 to a maximum of 15 patients depending on tolerance of therapy. The treatment period will last for approximately 1 day and the follow-up portion of the study will last 5 years.


Study summary:

If the patient has met all the eligibility criteria, they will be registered to the study After successful registration to the study and treatment planning session, patients will receive a single fraction of radiation. The total dose a particular patient receives will depend on the dose cohort they are enrolled into. Each treatment will last about one hour and will be given in a particular position to help guide the beams of radiation toward the cancer area. Although it is not mandatory, it is recommended that patients receive corticosteroid premedication (e.g. Decadron 4-10 m.g. p.o. in a single dose or equivalent) 15-60 minutes prior to each treatment for the intended purpose of modulating immediate acute inflammatory effects and providing anti-emetic support.


Criteria:

Inclusion Criteria: - Signed study specific informed consent form. - Age ≥ 18. - Zubrod Performance Status 0-2. - Biopsy proven primary malignancy. - Predicted survival of >6 months. - AJCC Stage IV disease with up to 5 liver metastases as seen on a contrast- enhanced CT, MRI or PET/CT. - Ability to spare a critical liver volume as defined by the protocol constraints. - Tumors must be located outside the Central Liver Zone defined by contouring the portal vein to its bifurcation + a 3-dimensional 2cm margin Exclusion Criteria: - Patients with a history of prior irradiation or other treatment to the liver or abdomen who after the protocol treatment would have cumulative doses to the liver or other normal tissues greater than the protocol defined constraints. - Need or plans for concomitant antineoplastic therapy (including surgery, cryotherapy, radiofrequency ablation, chemo-embolization, conventionally fractionated radiotherapy, brachytherapy, and hepatic artery chemotherapy) for the protocol treated lesions except at progression. Adjuvant systemic therapy before and after the protocol therapy per section 7.0, and surgery or other ablative therapy is allowed for lesions appearing after enrollment to this protocol as per section 8.0 is allowed. - Germ cell or hematologic malignancies. - History of Crohn's Disease or Ulcerative Colitis. - Active peptic ulcer disease. - Underlying hepatic cirrhosis with Child-Pugh class B or C - A major psychiatric illness which would limit understanding of the proposed protocol treatment and consent process - Men and women of reproductive potential may not participate unless they agree to use an effective contraceptive method. - Pregnant or lactating women. - Severe, active co-morbidity - Abnormal labs


NCT ID:

NCT01162278


Primary Contact:

Principal Investigator
Jeffrey Meyer, MD
University of Texas, Southwestern Medical Center at Dallas


Backup Contact:

N/A


Location Contact:

Dallas, Texas 75390
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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