Stereotactic Body Radiation Therapy (SBRT) in the Treatment of Liver Tumors

Alberta Health services

Status and phase: Unknown; Phase 2

Conditions: Liver Tumors

Treatments: Radiation: Stereotactic Body Radiation Therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT00691691

18740

Details and patient eligibility

About

Patients with primary hepato-biliary malignancies or liver metastases from gastrointestinal cancer suffer substantial morbidity and mortality from their hepatic disease. Curative resection is feasible only for selected subgroups of patients. The majority of patients have unresectable and incurable disease. Aggressive arterial and systemic chemotherapy have been used in recent years with improved response and survival. However, a significant number of patients, at least one-third of patients with liver metastases from colorectal cancer and two-third or higher of unresectable hepatobiliary cancer, continue to die of liver failure from progressive disease in the liver. Percutaneous ethanol injections, chemoembolization, cryotherapy and thermal ablation using radiofrequency have been used to treat selected patients with smaller tumors (3-4 cm) in areas away from major blood vessels and the biliary tract. However, most unresectable liver cancers did not fit the criteria for these treatments. Therefore, other regional therapeutic option like external radiation therapy may be considered for local control in the liver or symptom palliation

Enrollment: 71 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically conformation of liver malignancy
• Solitary or multiple liver tumors amenable to SBRT
• No jaundice or liver dysfunction
• For metastases, the primary tumor site has been adequately treated.
• For primary hepatoma, no extra-hepatic disease
• Karnofsky > 70

Exclusion criteria

• no extra-hepatic disease
• Liver failure or inadequate liver function
• Ascites
• Previous radiation therapy to the liver
• lesions invading major blood vessels in the porta region
• Contraindication to receive radiation therapy in the liver

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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71 participants in 1 patient group

1

Experimental group

Description:

Eligible patient will be treated with 48 Gy in 4 fractions encompassing the entire target lesion in 2 weeks with a minimum of 48 hours between each dose.

Treatment:

Radiation: Stereotactic Body Radiation Therapy