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Combination Chemotherapy, Interferon Alfa, and Interleukin-2 in Treating Patients With Metastatic Melanoma

TREATMENT OF METASTATIC MELANOMA WITH DTIC, CDDP AND IFN ALPHA WITH OR WITHOUT IL-2: A RANDOMIZED PHASE III TRIAL

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002669
Enrollment
90
Registered
2003-04-11
Start date
1995-06-30
Completion date
Unknown
Last updated
2012-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma (Skin)

Keywords

stage IV melanoma, recurrent melanoma

Brief summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Interferon alfa may interfere with the growth of the cancer cells. Interleukin-2 may stimulate a person's white blood cells to kill melanoma cells. It is not yet known which treatment regimen is more effective in treating melanoma. PURPOSE: Randomized phase II trial to compare the effectiveness of two regimens of combination chemotherapy plus interferon alfa and interleukin-2 in treating patients who have metastatic melanoma.

Detailed description

OBJECTIVES: * Assess the rate of disease stabilization in patients with metastatic melanoma when treated with interferon alfa, dacarbazine, cisplatin, and interleukin-2. * Assess toxicity, overall response rate, and response duration in these patients when treated with this regimen. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to center. Patients are randomized to one of two treatment arms. * Arm I: Patients receive dacarbazine IV over 1 hour and cisplatin IV over 3 hours on days 1-3. Patients also receive interferon alfa subcutaneously (SQ) on days 1-5 and interleukin-2 by continuous IV infusion on days 4-9. Treatment continues every 28 days for a maximum of 4 courses in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive dacarbazine IV on day 1 and 22 every 28 days for 2 courses. Patients then receive treatment as in arm I for a maximum of 4 courses. Patients are followed every 2 months for 6 months, then every 3 months thereafter. PROJECTED ACCRUAL: A total of 42-90 patients will be accrued for this study.

Interventions

BIOLOGICALaldesleukin
BIOLOGICALrecombinant interferon alfa
DRUGcisplatin
DRUGdacarbazine

Sponsors

European Organisation for Research and Treatment of Cancer - EORTC
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed melanoma that is metastatic and unresectable * Measurable, progressive disease (by physical exam and/or noninvasive imaging) * No prior irradiation of indicator lesions * No CNS metastases (confirmed by CT or MRI) PATIENT CHARACTERISTICS: Age: * 18 to 70 Performance status: * Karnofsky 60-100% Life expectancy: * Greater than 3 months Hematopoietic: * WBC at least 2,500/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic: * No serious hepatic disease Renal: * Creatinine no greater than 1.65 mg/dL * No serious renal disease Cardiovascular: * No serious cardiac disease Pulmonary: * No serious pulmonary disease Other: * No organ allograft * No autoimmune disease * No uncontrolled infection * No active peptic ulcer * No hyper or hypothyroidism * No requirement for corticosteroids * No second malignancy except basal cell skin carcinoma or carcinoma in situ of the cervix * Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior immunotherapy with interleukin-2 * No prior interferon alfa in combination with cisplatin or dacarbazine Chemotherapy: * No prior chemotherapy with cisplatin in combination with dacarbazine * More than 3 months since prior chemotherapy Endocrine therapy: * Not specified Radiotherapy: * Prior radiotherapy allowed Surgery: * Not specified

Countries

Austria, Belgium, France, Germany, Italy, Netherlands, Portugal, Switzerland, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026