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(L773:0012 1797 OR L773:1939 327X) srt2:(2005-2009)
 

Sökning: (L773:0012 1797 OR L773:1939 327X) srt2:(2005-2009) > (2006) > Autoimmune antibodi...

Autoimmune antibodies and recurrence-free interval in melanoma patients treated with adjuvant interferon.

Bouwhuis, Marna G (författare)
Suciu, Stefan (författare)
Collette, Sandra (författare)
visa fler...
Aamdal, Steinar (författare)
Kruit, Wim H (författare)
Bastholt, Lars (författare)
Stierner, Ulrika, 1952 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Salès, François (författare)
Patel, Poulam (författare)
Punt, Cornelis J A (författare)
Hernberg, Micaela (författare)
Spatz, Alain (författare)
ten Hagen, Timo L M (författare)
Hansson, Johan (författare)
Karolinska Institutet
Eggermont, Alexander M M (författare)
visa färre...
 (creator_code:org_t)
2009-06-16
2009
Engelska.
Ingår i: Journal of the National Cancer Institute. - : Oxford University Press (OUP). - 1460-2105 .- 0027-8874. ; 101:12, s. 869-77
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Appearance of autoantibodies and clinical manifestations of autoimmunity in melanoma patients treated with adjuvant interferon (IFN)-alpha2b was reported to be associated with improved prognosis. We assessed the association of the appearance of autoantibodies after initiation of treatment with recurrence-free interval in two randomized trials that compared intermediate doses of IFN with observation for the treatment of melanoma patients. METHODS: Serum levels of anticardiolipin, antithyroglobulin, and antinuclear antibodies were determined using enzyme-linked immunosorbent assays in 187 and 356 patients in the European Organization for Research and Treatment of Cancer (EORTC) 18952 and Nordic IFN trials, respectively, immediately before and up to 3 years after random assignment. The association of the presence of at least one of the three autoantibodies with risk of recurrence was assessed by three Cox models in patients negative for all three autoantibodies at baseline (125 from the EORTC 18952 trial and 230 from the Nordic IFN trial): 1) a model that considered appearance of autoantibodies as a time-independent variable, 2) one that considered a patient autoantibody positive once a positive test for an autoantibody was obtained, and 3) a model in which the status of the patient was defined by the most recent autoantibody test. All statistical tests were two-sided. RESULTS: When treated as a time-independent variable (model 1), appearance of autoantibodies was associated with improved relapse-free interval in both trials (EORTC 18952, hazard ratio [HR] = 0.41, 95% confidence interval [CI] = 0.25 to 0.68, P < .001; and Nordic IFN, HR = 0.51, 95% CI = 0.34 to 0.76, P < .001). However, on correction for guarantee-time bias, the association was weaker and not statistically significant (model 2: EORTC 18952, HR = 0.81, 95% CI = 0.46 to 1.40, P = .44; and Nordic IFN, HR = 0.85, 95% CI = 0.55 to 1.30, P = .45; model 3: EORTC 18952, HR = 1.05, 95% CI = 0.59 to 1.87, P = .88; and Nordic IFN, HR = 0.78, 95% CI = 0.49 to 1.24, P = .30). CONCLUSIONS: In two randomized trials of IFN for the treatment of melanoma patients, appearance of autoantibodies was not strongly associated with improved relapse-free interval when correction was made for guarantee-time bias.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Adjuvants
Immunologic
administration & dosage
therapeutic use
Adult
Aged
Antibodies
Anticardiolipin
blood
Antibodies
Antinuclear
blood
Autoantibodies
blood
Bias (Epidemiology)
Confounding Factors (Epidemiology)
Disease-Free Survival
Enzyme-Linked Immunosorbent Assay
Female
Humans
Interferon-alpha
administration & dosage
therapeutic use
Male
Melanoma
drug therapy
immunology
Middle Aged
Odds Ratio
Proportional Hazards Models
Randomized Controlled Trials as Topic
Skin Neoplasms
drug therapy
immunology
Time Factors

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