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A closer look at non Hodgkin's lymphoma cases in a national Swedish Systemic Lupus Erythematosus cohort - A nested case-control study
  1. Björn Lövström (bjorn.lofstrom{at}dll.se)
  1. Mälarsjukhuset, Eskilstuna, Sweden
    1. Carin Backlin (carin.backlin{at}genpat.uu.se)
    1. Dep of Genetics and Pathology, Uppsala University, Sweden
      1. Christer Sundström (christer.sundstrom{at}genpat.uu.se)
      1. Dep of Genetics and Pathology, Uppsala University, Sweden
        1. Anders Ekbom (anders.ekbom{at}medks.ki.se)
        1. Clinical Epidemiology Unit, Karolinska Institutet, Karolinska University Hospital at Solna, Sweden
          1. Ingrid E Lundberg (ingrid.lundberg{at}ki.se)
          1. Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital at Solna, Sweden

            Abstract

            Objective: To investigate risk factors for non-Hodgkin's lymphoma (NHL), analyse NHL subtypes and characteristics in patients with Systemic Lupus Erythematosus (SLE).

            Methods: A national SLE cohort identified through SLE discharge diagnoses in the Swedish hospital discharge register during 1964 to 1995 (n=6438) was linked to the national cancer register. A nested case control study on SLE patients who developed non-Hodgkin's lymphoma (NHL) during this observation period was performed with SLE patients without malignancy as controls. Medical records from cases and controls were reviewed. Tissue specimens on which the lymphoma diagnosis was based were retrieved and reclassified according to the WHO classification. NHLs of the subtype diffuse large B-cell lymphoma (DLBCL) were subject to additional immunohistochemical staining using antibodies against bcl-6, CD10, and IRF-4 for further subclassification into germinal centre (GC) or non-GC subtypes.

            Results: 16 patients with SLE had NHL, and the DLBCL subtype dominated (10 cases). Five-year overall survival and mean age at NHL diagnosis were comparable to NHL in the general population -50% and 61 years respectively. Cyclophosphamide or azathioprine use did not significantly elevate lymphoma risk, but so did haematological manifestations, sicca symptoms and pulmonary involvement. Two patients had DLBCL-GC subtype and an excellent prognosis.

            Conclusions: NHL in this national SLE-cohort was predominated by the aggressive DLBCL subtype. The prognosis of NHL was comparable to that of the general lymphoma population. There were no indications of treatment induced lymphomas. Molecular subtyping could be a helpful tool to predict prognosis also in SLE-patients with DLBCL.

            • diffuse large B-cell lymphoma
            • immunohistochemistry
            • non Hodgkin´s lymphoma
            • prognosis
            • systemic lupus erythematosus

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