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Published on: March 24, 2015
Patient preferences for adjuvant interferon alfa-2b treatment
K L Kilbridge1, J C Weeks, A J Sober
1Department of Health Evaluation Sciences, University of Virginia Health System, Charlottesville, VA 22908-0821, USA. kk4h@virginia.edu
Patients value recurrence-free survival more than interferon toxicity. Melanoma patients would tolerate significant interferon side effects for improved disease-free survival, indicating quality of life is paramount.
Area of Science:
- Oncology
- Health Economics
- Patient-Reported Outcomes
Background:
- Adjuvant interferon alfa-2b (IFN alpha-2b) shows potential for improving disease-free survival in high-risk melanoma.
- Significant toxicity of IFN alpha-2b limits its widespread use.
- Quantifying patient preferences for survival benefits versus treatment toxicity is crucial.
Purpose of the Study:
- To assess patient utilities for health states associated with adjuvant IFN alpha-2b therapy.
- To quantify the trade-offs between IFN alpha-2b toxicity and survival benefits.
- To inform clinical trial quality-of-life determinations for adjuvant IFN alpha-2b.
Main Methods:
- Utilities for health states were assessed in 107 low-risk melanoma patients using the standard gamble technique.
- Health states included IFN alpha-2b toxicity scenarios and posttreatment outcomes (disease-free health, recurrence, cancer death).
- Patients indicated required improvement in 5-year disease-free survival to tolerate IFN toxicity.
Main Results:
- Patient utilities for melanoma recurrence were significantly lower than for any IFN alpha-2b toxicity.
- Half of patients would tolerate mild-moderate toxicity for a 4% improvement in 5-year disease-free survival.
- Half of patients would tolerate severe toxicity for a 10% improvement in 5-year disease-free survival.
Conclusions:
- Melanoma recurrence is rated by patients as having a much lower quality of life than severe IFN alpha-2b toxicity.
- Recurrence-free survival is highly valued by patients.
- Measured utilities can be used in clinical trials to determine the net benefit of adjuvant IFN alpha-2b therapy.
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