首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >The relationship between cancer and medication exposures in systemic lupus erythaematosus: a case-cohort study.
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The relationship between cancer and medication exposures in systemic lupus erythaematosus: a case-cohort study.

机译:全身性红斑狼疮的癌症与药物暴露之间的关系:一项病例研究。

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OBJECTIVE: To examine if, in systemic lupus erythaematosus (SLE), exposure to immunosuppressive therapy (cyclophosphamide, azathioprine, methotrexate) increases cancer risk. METHODS: 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 (everever) and as time-dependent. RESULTS: 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). CONCLUSIONS: 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.
机译:目的:检查在系统性红斑狼疮(SLE)中,接受免疫抑制疗法(环磷酰胺,硫唑嘌呤,甲氨蝶呤)是否会增加患癌症的风险。方法:在多站点国际SLE队列中进行了病例队列研究。将受试者与区域肿瘤登记处联系起来,以确定进入该队列后发生的癌症病例。我们在控制其他药物(抗疟疾药物,全身性糖皮质激素,非甾体抗炎药(NSAIDs),阿司匹林),吸烟,年龄的模型中,计算了接触免疫抑制药物后癌症的危险比(HR)。 ,性别,种族/民族,地理位置,日历年,SLE病程和狼疮损害评分。在主要分析中,对暴露进行了分类(从不/从不)并且与时间相关。结果:结果来自246例癌症病例和538例无癌症的对照。任何免疫抑制药物治疗后的总体癌症风险调整后的HR为0.82(95%CI 0.50-1.36)。年龄大于或等于65岁,以及存在非恶性肿瘤损害与总体癌症风险相关。对于肺癌(n = 35例),吸烟也是一个重要的危险因素。特别是在检查血液学癌症时(n = 46例),提示免疫抑制药物暴露后风险增加,尤其是当这些药物滞后5年时(校正后的HR 2.29,95%CI 1.02-5.15)。结论:在我们的SLE样本中,年龄≥65岁,损害和烟草接触与癌症风险相关。尽管免疫抑制疗法可能不是整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。未来的研究正在进行中,以评估药物暴露和疾病活动对恶性肿瘤风险的独立影响。

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