Hector-Study to Evaluate the Efficacy of Octreotide in Patients With Inoperable Hepatocellular Carcinoma

• Status: Completed
• Trial end date: 2003-02-01
• Target enrollment: 0
• Participant gender: All

Summary

A preliminary study has shown that the hormone-similar, growth-retarding drug octreotide can prolong survival time in patients with primary liver cancer. Due to methodological deficiencies of the preliminary study the results will be re-checked by the comparison of octreotide with an pseudo-drug (so-called placebo) primarily regarding to the survival time and secondarily concerning costs, side effects, patient cooperation and quality of life as well as specific conditions in the tumor tissue in both groups with 108 patients with primary liver cancer.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University Hospital Freiburg
• Collaborators: Deutsche Krebshilfe e.V., Bonn (Germany); German Federal Ministry of Education and Research; Novartis
• Treatments: Octreotide; Somatostatin

Criteria

Inclusion Criteria:

• Inoperable patients

• histologically confirmed HCC or patients who refuse surgery and who otherwise (e.g. due to the advanced tumor stage) are not applicable for palliative local therapy (e.g. PEI, TACE, RFTA).

• Age: 18 years or older

Exclusion Criteria:

General:

• Patient with symptomatic Cholecyst-/Choledocholithiasis

• Patient with severe psychiatric disease.

• Participation in another clinical trial within the last 4 weeks.

• Simultaneous participation in another clinical examination.

• Legally incapacitated patient, who is not able, to understand nature, meaning and consequence of the study.

• Continuous drug or alcohol abuse.

• Patient with known HIV infection and antiretroviral therapy.

• Patient with not controllable infection disease.

• Pregnancy.

Study- and indication-specific exclusion criteria:

• Secondary malignant tumor without complete remission.

• Secondary malignant tumor with complete remission but current adjuvant therapy.

• Preliminary or current therapy with tamoxifen

• Pretreatment of the HCC.

• First-time diagnosis > 6 months before inclusion into the study.

• Severe hepatic encephalopathy, refractory to any treatment.

• Patients with operable HCC.

• Contraindication to i.m. injections.

• Hypersensitivity to octreotide.