Immunochemotherapy for Metastatic Renal Cell Carcinoma

Adenocarcinoma Clear Cell Clinical Trial

Official title:

Interleukin-2, Interferon Alpha,Capecitabine and Vinblastin for Treatment of Metastatic Renal Cell Carcinoma: A Multicenter Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00226798
• Other study ID #: 1747CTIL
• Secondary ID: Raphael Rubinov
• Status: Recruiting
• Phase: Phase 2
• First received: September 26, 2005
• Last updated: December 31, 2005
• Start date: December 2003
• Est. completion date: September 2005

Study information

• Verified date: September 2005
• Source: Rambam Health Care Campus
• Contact: Eliahu Gez, MD
• Phone: 972-4-8542012
• Email: e_gez[@]rambam.health.gov.il
• Is FDA regulated: No
• Health authority: Israel: Israeli Health Ministry Pharmaceutical Administration
• Study type: Interventional

Clinical Trial Summary

Immunochemotherapy consisting of IL-2, INF-A, and VBL and 5FU is regarded as the treatment of choice in metastatic renal cell carcinoma. During the period 1996-2000, we evaluated the efficacy and toxicity of this immunochemotherapy, combined with an aggressive surgical approach: nephrectomy before treatment and resection of residual disease. The 3-year survival rate for the entire group and complete responder patients was 30% and 88%, respectively. The side effects were usually moderate and consisted mainly of a flu-like syndrome, headache, nausea, vomiting and depression. Most importantly, there was no drug-related death. Good performance status, absence of bone metastases and prior nephrectomy were associated with higher response rates.

Capecitabine is a novel fluoropyrimidine carbamate, orally administered and selectively activated to Fluorouracil by a sequential triple-enzyme pathway in liver and tumor cells. Capecitabine at dose of 2,500mg/m2/d divided equally into two daily doses for 14 days in patients who failed to respond to “standard” immunotherapy achieved a 30% objective response. Toxicity consisted of hand-foot syndrome.

Aim of Study:

To evaluate efficacy and toxicity of the combination of IL-2, INF-A, VBL and Capecitabine in MRCC

Description:

This is a phase II study, non-randomized in patients with metastatic renal cell carcinoma. The treatment will include: Proleukin (produced by Chiron and supplied by Megapharm Israel Ltd), Roferon A and Xeloda (produced by Roche) and VBL. The treatment will be given in 8-week courses with an interval of two weeks of rest in which the response (on D63) and toxicity will be assessed.

45 patients with MRCC will be entered into this study during a 18-month period. All patients must meet all inclusion and exclusion criteria. All data of each participating patient, including medical history, disease characteristics, laboratory and imaging tests, response and toxicity to treatment will be entered into the specific form before, during, after each treatment course and during follow up.

Patients will be followed up for survival status and disease status every 6 months until last visit or death.

Treatment Schedule:

Proleukin S.C. 10X106 IU/m2 three times a week (Sun, Tue, Thu), weeks 1 – 4 Roferon A S.C. 6 X 106 IU/m2 once a week (Wed), weeks 1 – 4 Roferon A S.C. 3 X 106 IU/m2 three times a week, weeks 5 – 8 Xeloda Oral 1,000 mg/m2 twice a day, weeks 5, 6 Vinblastine I.V. 4mg/m2, Day 1, weeks 5 &

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: September 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Inclusion Criteria; Patients with the following criteria will be included in this study

• Pathological (histology or cytology) diagnosis of renal cell carcinoma

• Clinical evidence of metastatic disease

• Performance status 0 – 2 (European Cooperative Oncology Group Score)

• Nephrectomy before starting treatment

• Normal cardiac function (left ventricular ejection fraction >45%).

• Normal blood counts: WBC >3,000/ml3, Hb >10gr%, Platelets >100,000/ml3

• Normal kidney function: Creatinine <1.3 mg/dl

• Age ? 18 years

• Patient’s written consent (on informed consent form)

Exclusion Criteria:

• Life expectancy less than 3 months

• Brain metastases

• Ischemic heart disease – active

• Prior immunochemotherapy

• Performance status 3 or more (European Cooperative Oncology Group Score)

• Schizophrenia

• Active liver disease

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Adenocarcinoma
• Adenocarcinoma Clear Cell
• Carcinoma, Renal Cell

Intervention

Drug:
• Capecitabine (Xeloda)

Locations

Country	Name	City	State
Israel	Rambam medical Center	Haifa

Sponsors (2)

Lead Sponsor	Collaborator
Rambam Health Care Campus	Roche Pharma AG

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective response
Secondary	Toxicity