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Clinical Trial Summary

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. This may be an effective treatment for liver cancer.

PURPOSE: This phase I/II trial is studying the side effects and best dose of external-beam radiation therapy in treating patients with liver cancer that cannot be removed by surgery.


Clinical Trial Description

OBJECTIVES:

- To assess the feasibility and safety of radiotherapy (RT) in patients with hepatocellular carcinoma. (Phase I)

- To assess the safety and efficacy of RT in these patients. (Phase II)

- To generate reproducible peptide patterns of the serum proteome or specific serum sub proteomes in these patients.

- To assess changes in the proteome or sub proteome patterns after RT in these patients.

- To detect peptides that discriminate between before and after RT in these patients.

- To identify these discriminating peptides in these patients.

OUTLINE: This is a multicenter, phase I dose-escalation study followed by a phase II study.

Patients undergo radiotherapy (RT) once daily, five days a week, for 6 weeks. Intensity-modulated, 3-dimensional conformal, or fractionated stereotactic RT may be used.

After completion of study therapy, patients in the phase I portion are followed for 1 year and patients in the phase II portion are followed for 3 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00777894
Study type Interventional
Source Swiss Group for Clinical Cancer Research
Contact
Status Completed
Phase Phase 1/Phase 2
Start date November 2008
Completion date December 2015

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