Löfström B, Backlin C, Sundström C, Ekbom A, Lundberg I E
Department of Rheumatology, Malar Hospital, SE 631 88 Eskilstuna, Sweden.
Ann Rheum Dis. 2007 Dec;66(12):1627-32. doi: 10.1136/ard.2006.067108. Epub 2007 May 21.
To investigate risk factors for non-Hodgkin's lymphoma (NHL) and analyse NHL subtypes and characteristics in patients with systemic lupus erythematosus (SLE).
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 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.
16 patients with SLE had NHL, and the DLBCL subtype dominated (10 cases). The 5-year overall survival and mean age at NHL diagnosis were comparable with NHL in the general population-50% and 61 years, respectively. Cyclophosphamide or azathioprine use did not elevate lymphoma risk, but the risk was elevated if haematological or sicca symptoms, or pulmonary involvement was present in the SLE disease. Two patients had DLBCL-GC subtype and an excellent prognosis.
NHL in this national SLE cohort was predominated by the aggressive DLBCL subtype. The prognosis of NHL was comparable with 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.
探讨非霍奇金淋巴瘤(NHL)的危险因素,并分析系统性红斑狼疮(SLE)患者的NHL亚型及特征。
通过瑞典医院出院登记册中1964年至1995年期间的SLE出院诊断确定的全国SLE队列(n = 6438)与国家癌症登记册相链接。对在此观察期内发生NHL的SLE患者进行巢式病例对照研究,以无恶性肿瘤的SLE患者作为对照。回顾病例和对照的病历。检索基于淋巴瘤诊断的组织标本,并根据世界卫生组织分类进行重新分类。对弥漫性大B细胞淋巴瘤(DLBCL)亚型的NHL,使用抗bcl-6、CD10和IRF-4抗体进行额外的免疫组化染色,以进一步分为生发中心(GC)或非GC亚型。
16例SLE患者患有NHL,以DLBCL亚型为主(10例)。NHL诊断时的5年总生存率和平均年龄与普通人群中的NHL相当,分别为50%和61岁。使用环磷酰胺或硫唑嘌呤并未增加淋巴瘤风险,但如果SLE疾病存在血液学或干燥症状或肺部受累,则风险会增加。2例患者为DLBCL-GC亚型,预后良好。
该全国SLE队列中的NHL以侵袭性DLBCL亚型为主。NHL的预后与一般淋巴瘤人群相当。没有治疗诱导淋巴瘤的迹象。分子亚型分析可能也是预测SLE合并DLBCL患者预后的有用工具。