The primary objective of this study is to quantify and compare the prevalence of adverse events (AEs) in patients with stage III melanoma before and after initiation of interferon (IFN) therapy in a real-world setting. A secondary objective is to quantify annual costs and resource utilization before and after IFN initiation among patients with stage III melanoma in a real-world setting.
Study Type
OBSERVATIONAL
Enrollment
436
Prevalence of depression in patients with stage III melanoma before initiation of Interferon alfa-2b (IFN) therapy
Time frame: 180 days prior to the index date
Prevalence of depression in patients with stage III melanoma after initiation of IFN therapy
Time frame: 180 days after the index date
Prevalence of fatigue in patients with stage III melanoma before initiation of IFN therapy
Time frame: 180 days prior to the index date
Prevalence of fatigue in patients with stage III melanoma after initiation of IFN therapy
Time frame: 180 days after the index date
Prevalence of myalgia in patients with stage III melanoma before initiation of IFN therapy
Time frame: 180 days prior to the index date
Prevalence of myalgia in patients with stage III melanoma after initiation of IFN therapy
Time frame: 180 days after the index date
Pre-IFN treatment period Health care costs related to depression
Time frame: 180 days prior to the index date
Post-IFN treatment period Health care costs related to depression
Time frame: 180 days after the index date
Pre-IFN treatment period Health care costs related to fatigue
Time frame: 180 days prior to the index date
Post-IFN treatment period Health care costs related to fatigue
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Time frame: 180 days after the index date
Pre-IFN treatment period Health care costs related to myalgia
Time frame: 180 days prior to the index date
Post-IFN treatment period Health care costs related to myalgia
Time frame: 180 days after the index date