Bernatsky S, Joseph L, Boivin J-F, Gordon C, Urowitz M, Gladman D, Fortin P R, Ginzler E, Bae S-C, Barr S, Edworthy S, Isenberg D, Rahman A, Petri M, Alarcón G S, Aranow C, Dooley M-A, Rajan R, Sénécal J-L, Zummer M, Manzi S, Ramsey-Goldman R, Clarke A E
Division of Clinical Epidemiology, McGill University Health Centre, 687 Pine Avenue West, V-Building, Montreal, Québec H3A 1A1, Canada.
Ann Rheum Dis. 2008 Jan;67(1):74-9. doi: 10.1136/ard.2006.069039. Epub 2007 Jun 1.
To examine if, in systemic lupus erythaematosus (SLE), exposure to immunosuppressive therapy (cyclophosphamide, azathioprine, methotrexate) increases cancer risk.
A case-cohort study was performed within a multi-site international SLE cohort; subjects were linked to regional tumour registries to determine cancer cases occurring after entry into the cohort. We calculated the hazard ratio (HR) for cancer after exposure to an immunosuppressive drug, in models that controlled for other medications (anti-malarial drugs, systemic glucocorticoids, non-steroidal anti-inflammatory drugs (NSAIDs), aspirin), smoking, age, sex, race/ethnicity, geographic location, calendar year, SLE duration, and lupus damage scores. In the primary analyses, exposures were treated categorically (ever/never) and as time-dependent.
Results are presented from 246 cancer cases and 538 controls without cancer. The adjusted HR for overall cancer risk after any immunosuppressive drug was 0.82 (95% CI 0.50-1.36). Age > or = 65, and the presence of non-malignancy damage were associated with overall cancer risk. For lung cancer (n = 35 cases), smoking was also a prominent risk factor. When looking at haematological cancers specifically (n = 46 cases), there was a suggestion of an increased risk after immunosuppressive drug exposures, particularly when these were lagged by a period of 5 years (adjusted HR 2.29, 95% CI 1.02-5.15).
In our SLE sample, age > or = 65, damage, and tobacco exposure were associated with cancer risk. Though immunosuppressive therapy may not be the principal driving factor for overall cancer risk, it may contribute to an increased risk of haematological malignancies. Future studies are in progress to evaluate independent influence of medication exposures and disease activity on risk of malignancy.
研究在系统性红斑狼疮(SLE)患者中,接受免疫抑制治疗(环磷酰胺、硫唑嘌呤、甲氨蝶呤)是否会增加患癌风险。
在一个多中心国际SLE队列中进行了一项病例队列研究;将研究对象与区域肿瘤登记处进行关联,以确定进入队列后发生的癌症病例。在控制了其他药物(抗疟药、全身用糖皮质激素、非甾体抗炎药(NSAIDs)、阿司匹林)、吸烟、年龄、性别、种族/民族、地理位置、日历年份、SLE病程和狼疮损伤评分的模型中,我们计算了接触免疫抑制药物后患癌的风险比(HR)。在主要分析中,暴露情况按分类(曾经/从未)处理,并作为时间依赖性因素。
呈现了246例癌症病例和538例无癌症对照的结果。任何免疫抑制药物治疗后总体癌症风险的调整后HR为0.82(95%CI 0.50 - 1.36)。年龄≥65岁以及存在非恶性损伤与总体癌症风险相关。对于肺癌(35例),吸烟也是一个突出的危险因素。专门观察血液系统癌症(46例)时,提示免疫抑制药物暴露后风险增加,尤其是暴露滞后5年时(调整后HR 2.29,95%CI 1.02 - 5.15)。
在我们的SLE样本中,年龄≥65岁、损伤和烟草暴露与癌症风险相关。虽然免疫抑制治疗可能不是总体癌症风险的主要驱动因素,但它可能导致血液系统恶性肿瘤风险增加。正在进行进一步研究以评估药物暴露和疾病活动对恶性肿瘤风险的独立影响。