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
相关论文
共 27 条
[1]   ANALYSIS OF SURVIVAL BY TUMOR RESPONSE [J].
ANDERSON, JR ;
CAIN, KC ;
GELBER, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (11) :710-719
[2]   Prognostic factors analysis of 17,600 melanoma patients: Validation of the American Joint Committee on Cancer melanoma staging system [J].
Balch, CM ;
Soong, SJ ;
Gershenwald, JE ;
Thompson, JF ;
Reintgen, DS ;
Cascinelli, N ;
Urist, M ;
McMasters, KM ;
Ross, MI ;
Kirkwood, JM ;
Atkins, MB ;
Thompson, JA ;
Coit, DG ;
Byrd, D ;
Desmond, R ;
Zhang, YT ;
Liu, PY ;
Lyman, GH ;
Morabito, A .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3622-3634
[3]   Autoimmune Antibodies and Recurrence-Free Interval in Melanoma Patients Treated With Adjuvant Interferon [J].
Bouwhuis, Marna G. ;
Suciu, Stefan ;
Collette, Sandra ;
Aamdal, Steinar ;
Kruit, Wim H. ;
Bastholt, Lars ;
Stierner, Ulrika ;
Sales, Francois ;
Patel, Poulam ;
Punt, Cornelis J. A. ;
Hernberg, Micaela ;
Spatz, Alain ;
ten Hagen, Timo L. M. ;
Hansson, Johan ;
Eggermont, Alexander M. M. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2009, 101 (12) :869-877
[4]   Treating cancer with PEG intron - Pharmacokinetic profile and dosing guidelines for an improved interferon-alpha-2b formulation [J].
Bukowski, RM ;
Tendler, C ;
Cutler, D ;
Rose, E ;
Laughlin, MM ;
Statkevich, P .
CANCER, 2002, 95 (02) :389-396
[5]   Adjuvant therapy with pegylated interferon alfa-2b versus observation alone in resected stage III melanoma:: final results of EORTC 18991, a randomised phase III trial [J].
Eggermont, Alexander M. M. ;
Suciu, Stefan ;
Santinami, Mario ;
Testori, Alessandro ;
Kruit, Wim H. J. ;
Marsden, Jeremy ;
Punt, Cornelis J. A. ;
Sales, Francois ;
Gore, Martin ;
MacKie, Rona ;
Kusic, Zvonko ;
Dummer, Reinhard ;
Hauschild, Axel ;
Musat, Elena ;
Spatz, Alain ;
Keilholz, Ulrich .
LANCET, 2008, 372 (9633) :117-126
[6]   Serum concentrations of pegylated interferon α-2b in patients with resected stage III melanoma receiving adjuvant pegylated interferon α-2b in a randomized phase III trial (EORTC 18991) [J].
Eggermont, Alexander M. M. ;
Bouwhuis, Marna G. ;
Kruit, Wim H. ;
Testori, Alessandro ;
ten Hagen, Timo ;
Yver, Antoine ;
Xu, Christine .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 65 (04) :671-677
[7]   Post-surgery adjuvant therapy with intermediate doses of interferon alfa 2b versus observation in patients with stage IIb/III melanoma (EORTC 18952): randomised controlled trial [J].
Eggermont, AMM ;
Suciu, S ;
MacKie, R ;
Ruka, W ;
Testori, A ;
Kruit, W ;
Punt, CJA ;
Delauney, M ;
Sales, F ;
Groenewegen, G ;
Ruiter, DJ ;
Jagiello, I ;
Stoitchkov, K ;
Keilholz, U ;
Lienard, D .
LANCET, 2005, 366 (9492) :1189-1196
[8]   Pegylated interferon-α2b:: Pharmacokinetics, pharmacodynamics, safety, and preliminary efficacy data [J].
Glue, P ;
Fang, JWS ;
Rouzier-Panis, R ;
Raffanel, C ;
Sabo, R ;
Gupta, SK ;
Salfi, M ;
Jacobs, S .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 68 (05) :556-567
[9]   Prognostic significance of autoimmunity during treatment of melanoma with interferon [J].
Gogas, H ;
Ioannovich, J ;
Dafni, U ;
Stavropoulou-Giokas, C ;
Frangia, K ;
Tsoutsos, D ;
Panagiotou, P ;
Polyzos, A ;
Papadopoulos, O ;
Stratigos, A ;
Markopoulos, C ;
Bafaloukos, D ;
Pectasides, D ;
Fountzilas, G ;
Kirkwood, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (07) :709-718
[10]  
HANSSON J, 2007, EJC SUPPL, V6, P4