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多发性硬化症患者用硫唑嘌呤和疾病修正疗法治疗的癌症风险:意大利观察性研究。

Cancer risk for multiple sclerosis patients treated with azathioprine and disease-modifying therapies: an Italian observational study.

机构信息

Unit of Neuromotor Rehabilitation, Multiple Sclerosis Center, Fondazione Don Carlo Gnocchi IRCCS, Via Capecelatro, 66, 20148, Milano, Italy.

Unit of Neurology B, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.

出版信息

Neurol Sci. 2021 Dec;42(12):5157-5163. doi: 10.1007/s10072-021-05216-z. Epub 2021 Mar 31.

Abstract

BACKGROUND

The risk of malignancy associated with sequential disease-modifying therapies (DMTs) for patients with multiple sclerosis (MS) is uncertain. The aim of this study was to analyze the risk of cancer in patients with MS treated with azathioprine (AZA) and the influence of sequential DMTs on the risk.

METHOD

We retrospectively enrolled a cohort of AZA-treated MS patients followed in two Italian centers from 1987 to 2019. The ratio between observed and expected cancers in the Italian general population was calculated as standardized incidence ratio (SIR). Associations between AZA and DMTs and cancer were estimated by Cox proportional hazards model.

RESULTS

We identified 500 AZA-treated MS patients, followed for a median time of 9.7 (0.1-45.7) years: 61.8% of them were treated with DMTs. We found 22 cases of cancer (4.4%). The SIR was 1.14 (95% CI 0.98-1.29), not significantly increased in comparison with the general population. However, the risk was significantly higher in the quintiles of age 32-45, SIR 1.21 (95% CI 1.21-1.42), and 46-51, SIR 1.11 (95% CI 1.11-1.32) than in older cases. Age at AZA treatment onset was the only covariate significantly related to cancer incidence (HR = 1.049, 95% CI 1.007-1.093). The exposure to other DMTs did not modify the risk.

CONCLUSION

The risk of malignancy in MS patients after AZA was similar to that of the general population and did not change with other DMTs sequential treatments. The increased risk in the younger ages should be considered in treatment assessment.

摘要

背景

对于多发性硬化症(MS)患者,连续使用疾病修正疗法(DMT)相关的恶性肿瘤发病风险尚不确定。本研究旨在分析接受硫唑嘌呤(AZA)治疗的 MS 患者发生癌症的风险,以及连续使用 DMT 对该风险的影响。

方法

我们回顾性地纳入了自 1987 年至 2019 年在意大利的两个中心接受 AZA 治疗的 MS 患者队列。通过标准化发病比(SIR)计算意大利普通人群中观察到的癌症与预期癌症的比值。使用 Cox 比例风险模型估计 AZA 和 DMT 与癌症之间的关联。

结果

我们确定了 500 名接受 AZA 治疗的 MS 患者,中位随访时间为 9.7(0.1-45.7)年:其中 61.8%的患者接受了 DMT 治疗。我们发现了 22 例癌症病例(4.4%)。SIR 为 1.14(95%CI 0.98-1.29),与普通人群相比无显著增加。然而,在年龄 32-45 岁的五分位数中,SIR 为 1.21(95%CI 1.21-1.42)和 46-51 岁的五分位数中,SIR 为 1.11(95%CI 1.11-1.32)的风险明显更高。AZA 治疗开始时的年龄是唯一与癌症发病率显著相关的协变量(HR=1.049,95%CI 1.007-1.093)。接受其他 DMT 治疗不会改变风险。

结论

AZA 治疗后 MS 患者发生恶性肿瘤的风险与普通人群相似,且不会因其他 DMT 序贯治疗而改变。在评估治疗时应考虑年龄较小患者的风险增加。

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