Journal
JOURNAL OF CLINICAL ONCOLOGY
Volume 20, Issue 5, Pages 1311-1318Publisher
AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.20.5.1311
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Funding
- NCI NIH HHS [CA12449, CA39229, CA32291, CA23318, CA80775, CA66636, CA73590, CA21115] Funding Source: Medline
- NATIONAL CANCER INSTITUTE [U10CA021115, U10CA012449, U10CA039229, U10CA073590, U10CA032291, U10CA080775, U10CA066636, U10CA023318] Funding Source: NIH RePORTER
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Purpose: High-dose adjuvant interferon alfa-2b (IFNalpha2b) for high-risk melanoma is a 1-year regimen that improves relapse-free and overall survival but has significant toxicity. A quality-of-life-adjusted survival (QAS) analysis analysis of two cooperative group phase III trials, E1684 and E1690/S9111/C9190, was performed, incorporating patient values (utilities) for the toxicity of IFNa2b treatment and melanoma recurrence. Patients and Methods. Quality-Adjusted Time Without Symptoms or Toxicity methodology was used with melanoma patient utilities and trial data to estimate the effect of IFNa2b on QAS. The increase or decrease in QAS that patients could expect from treatment was estimated based on their utilities. Eleven utility predictor questions were tested to identify patients with utilities that result in decreased QAS. Results: Using E1684 data, IFNa2b would result in an increase in QAS for all sets of patient utilities. This benefit was significant (P < .05) for 16% of patients. Using E1690/S9111/C9190 data, 77% of patients would experience a benefit in QAS from IFNa2b and 23% would experience a decrease in QAS; neither of these effects was statistically significant. Using utility predictors and the E1690/S9111/C9190 analysis, a decision rule was formulated that helps identify patients in whom IFNa2b may detract from QAS. Conclusion: Most patients experienced improvement in GAS in both trials, but this benefit was statistically significant in only 16% of patients in E1684. Change in QAS depends more on the utility for IFNa2b toxicity than on the utility for melanoma recurrence. Cancer patients probably have higher utilities for IFNa2b toxicity than members of the general population and will tend to favor IFNa2b treatment as a result. (C) 2002 by American Society of Clinical Oncology.
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