NCT Number: NCT00308607
Bevacizumab, Dacarbazine and Interferon-Alfa to Treat Metastatic Melanoma
The purpose of this study is to determine whether combination therapy with bevacizumab (Avastin), dacarbazine and interferon-alfa-2a (Roferon-A) is effective in patients with locally advancing or metastatic melanoma.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Kuopio University Hospital, Kuopio, Finland
About this study
Dacarbazine (DTIC) has been approved for treating metastatic melanoma in the 1970s, and after that numerous schedules and dacarbazine-based combinations have been studied in this disease. DTIC as a single agent gives a response rate of only 20%, but there have been efforts to improve this poor result by using DTIC in different combinations.Treatment of melanoma with combination chemotherapy and interferon-α (IFN-α) has given 50-60% response rates,but increase in the overall survival time has not been reached in controlled phase III studies. Thus, standard reference therapy in treatment of metastatic melanoma still is single dacarbazine or its combination with s.c. IFN-α. In addition, new studies with melanoma cells in vitro show that dacarbazine causes transcriptional up-regulation of vascular endothelial growth factor (VEGF), suggesting a potential clinical benefit of combination of DTIC and anti-VEGF therapy. IFN-α has been used in adjuvant therapy and in treatment of metastatic melanoma. IFN-α exerts its effects through antiproliferative, apoptosis-inducing and particularly antiangiogenic effects in addition to immunologic modulation.
The purpose of this study is to determine whether combination therapy with bevacizumab (Avastin), dacarbazine and interferon-alfa-2a (Roferon-A) can increase progression-free survival and overall survival in patients with locally advancing or metastatic melanoma.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- histologically confirmed malignant melanoma either locally progressing inoperable or metastatic
- measurable/evaluable disease in accordance with RECIST criteria
- WHO performance status 0-2
- normal organ function
- signed written informed consent
Exclusion criteria
- unevaluable disease
- major surgery within 28 days prior to day 0
- uncompleted radiotherapy
- CNS metastases
- serious non-healing wound or ulcer
- bleeding diathesis or coagulopathy
- uncontrolled hypertension
- clinically significant cardiovascular disease
- depression or psychosis, which needs medication
- ongoing treatment with aspirin (>325 mg/day)
- pregnancy
- any other serious or uncontrolled illness
- previous chemotherapy for metastatic melanoma
Treatment and study plan
Dacarbazine
Druginterferon-alfa-2a (Roferon-A)
DrugPrimary outcomes
-
Response rate according to RECIST criteria
-
Progression-free survival
-
Time to brain metastases
-
Overall survival
Secondary outcomes
-
To evaluate safety of this combination after every two cycles
-
Serum analysis of particular biochemical markers
Sponsors and collaborators
Lead sponsor
University of Turku
Other
Registry information
Official study title
Bevacizumab, Dacarbazine and Interferon Alfa-2a Combination as a First-Line Therapy in Patients With Locally Advancing or Metastatic Melanoma
Important dates
- Study start
- 2005
- Primary completion
- 2008
- Study completion
- 2009
- First posted
- Mar 29, 2006
- Registry last updated
- Apr 3, 2009
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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