Phase III Trial Comparing Adjuvant Treatment With Pegylated Interferon Alfa-2b Versus Observation: Prognostic Significance of Autoantibodies-EORTC 18991

被引:57
|
作者
Bouwhuis, Marna G.
Suciu, Stefan
Testori, Alessandro
Kruit, Wim H.
Sales, Francois
Patel, Poulam
Punt, Cornelis J.
Santinami, Mario
Spatz, Alain
ten Hagen, Timo L. M.
Eggermont, Alexander M. M.
机构
[1] Erasmus Univ, Dept Surg, Div Surg Oncol, Dr Daniel Den Hoed Canc Ctr,Med Ctr, NL-3075 EA Rotterdam, Netherlands
[2] Erasmus Univ, Dept Med Oncol, Med Ctr, Dr Daniel Den Hoed Canc Ctr, NL-3075 EA Rotterdam, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, NL-6525 ED Nijmegen, Netherlands
[4] European Org Res & Treatment Canc EORTC Headquart, Dept Stat, Brussels, Belgium
[5] Inst Jules Bordet, Dept Surg, B-1000 Brussels, Belgium
[6] Natl Canc Inst, Dept Surg Oncol, European Inst Oncol, Dept Surg, I-20133 Milan, Italy
[7] St James Univ Hosp, Canc Res UK Clin Ctr, Leeds, W Yorkshire, England
[8] Inst Gustave Roussy, Dept Pathol, Villejuif, France
关键词
SYSTEMIC-LUPUS-ERYTHEMATOSUS; MELANOMA PATIENTS; ANTINUCLEAR ANTIBODIES; DIABETIC-KETOACIDOSIS; DOSE INTERFERON; THERAPY; ALPHA; AUTOIMMUNITY; CANCER;
D O I
10.1200/JCO.2009.24.6264
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Conflicting data have been reported concerning the prognostic value of autoimmune antibodies in patients with melanoma treated with adjuvant interferon alfa-2b (IFN). We evaluated the prognostic significance of autoantibodies in the European Organisation for Research and Treatment of Cancer 18991 trial, comparing long-term administration of pegylated IFN (PEG-IFN) with observation. Patients and Methods Anticardiolipin, antithyroglobulin, and antinuclear antibodies were determined by enzyme-linked immunosorbent assays in 296 patients before random assignment and every 6 months after random assignment for up to 5 years. Prognostic impact of autoantibodies on recurrence-free survival (RFS) was assessed using the following three Cox models: a model that considered autoantibody appearance as a time-independent variable (model 1); a model that considered a patient to be autoantibody positive from the first positive test (model 2); and a model in which the most recent autoantibody test was used to define the status of the patient (model 3). Results Patients who were autoantibody negative at baseline were analyzed (n = 220). Occurrence of autoantibodies during follow-up was higher in the PEG-IFN-treated patients (18% in the observation arm v 52% in the PEG-IFN arm). Autoantibody appearance was of prognostic importance by using model 1 (hazard ratio [HR] = 0.56; 95% CI, 0.36 to 0.87; P = .01). However, when guarantee-time bias was taken into account using model 2 (HR = 1.19; 95% CI, 0.75 to 1.88; P = .46) or method 3 (HR = 1.14; 95% CI, 0.71 to 1.83; P = .59), significance was lost. Results were similar when treatment groups were analyzed separately. Conclusion Appearance of autoimmune antibodies is neither a prognostic nor a predictive factor for improved outcome in patients with melanoma treated with PEG-IFN.
引用
收藏
页码:2460 / 2466
页数:7
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