Quality-of-life-adjusted survival analysis of high-dose adjuvant interferon alfa-2b for high-risk melanoma patients using intergroup clinical trial data

被引:58
作者
Kilbridge, KL
Cole, BF
Kirkwood, JM
Haluska, FG
Atkins, MA
Ruckdeschel, JC
Sock, DE
Nease, RF
Weeks, JC
机构
[1] Univ Virginia, Dept Hlth Evaluat Sci, Charlottesville, VA 22908 USA
[2] Washington Univ, St Louis, MO USA
[3] Univ S Florida, H Lee Moffitt Canc Ctr, Tampa, FL 33682 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Massachusetts Gen Hosp, Beth Israel Deaconess Med Ctr, Boston, MA 02114 USA
[6] Univ Pittsburgh, Pittsburgh, PA USA
[7] Dartmouth Hitchcock Med Ctr, Lebanon, NH 03766 USA
关键词
D O I
10.1200/JCO.20.5.1311
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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页码:1311 / 1318
页数:8
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