Combined Treatment With Capecitabine and Immunotherapy Versus Immunotherapy Alone in Advanced Renal Cell Carcinoma
Renal Cell Cancer
About this trial
This is an interventional treatment trial for Renal Cell Cancer focused on measuring renal cell cancer
Eligibility Criteria
Inclusion Criteria: Histologically confirmed renal cell carcinoma (primary tumour or biopsy/surgery of metastases) Radiologically confirmed metastatic disease Surgically removed primary tumour so feasible (nephrectomy or nephron-sparing surgery as indicated) Karnofsky-Performance Status >70% Age 19-75 years Life expectancy of at least 3 months Adequate bone marrow function (i.e. white blood cell count above 3000/μL, platelet count above 75 000 /μL, hemoglobin above 9 mg/dl) Adequate organ function (i.e. serum creatinine, bilirubin and AST below 1.25 x the upper limit of the institutions' normal range) Negative pregnancy test for female patients Written informed consent Exclusion Criteria: Age <19 or >75 years Karnofsky-Performance Status < 70% Untreated or uncontrolled brain metastases Second neoplasia Primary tumour surgically removable Solitary, surgically removable metastases Major concomitant diseases of the cardiovascular, respiratory or renal systems, as well as active systemic infections Severe renal disease or liver insufficiency or myeloid dysfunction (including patients with a history of a disease that is likely to interfere with the metabolism or excretion of the test medication) Other less common diseases as peptic ulcer disease, inflammatory bowel disease, autoimmune disease (severe known psoriasis, idiopathic thrombocytopenic purpura, lupus erythematosus, autoimmune hemolytic anemia, scleroderma, rheumatoid arthritis etc.) Drug addiction (including excessive alcohol consumption) within 1 year prior to study start. History of other conditions consistent with decompensated liver disease or other evidence of bleeding form esophageal varices. History of chronic hepatitis and immunsupressiva Known HIV Infection Evidence of allergy or hypersensitivity against recombinant Interferon alfa-2a or other components of preparation. History of severe psychiatric disease, especially depression. Severe psychiatric disease is defined as treatment with an antidepressant medication or a major tranquilizer at therapeutic doses for major depression or psychosis, respectively, for at least 3 months at any previous time or any history of the following: a suicidal attempt, hospitalization for psychiatric disease, or a period of disability due to a psychiatric disease. Seizure disorders and /or compromised central nervous system function. History of evidence of severe retinopathy Patient unwilling or unable to give informed consent Pregnancy or breastfeeding
Sites / Locations
- Univ. Klinik f. Innere Medizin, Abt. Onkologie
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Capecitabine and Interferon
Interferon
Combined Chemo-Immunotherapy Chemotherapy: Mo-Fr Immunotherapy
Patients randomized to group B will receive treatment according to the same treatment schedule and at the same dosages without capecitabine. Efficacy evaluations will be performed every 14 weeks of treatment in both groups