恶性黑色素瘤和多发性硬化症治疗:FDA不良事件报告系统的歧化分析。

IF 5
Alexandra Balshi, John P Dempsey, Nova Manning, Grace Leuenberger, Ursela Baber, Jacob A Sloane
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引用次数: 0

摘要

尽管全国范围内的队列研究显示多发性硬化症(PwMS)患者患恶性黑色素瘤(MM)的风险增加,但MS疾病改善疗法(dmt)与MM风险之间的联系仍未得到充分探讨。我们在FDA不良事件报告系统(FAERS)中确定了1200例MM与MS DMTs相关的报告,对所有DMTs的汇总分析显示,与所有其他FAERS药物相比,MM报告比例不成比例地高(报告优势比,2.30;95%置信区间为2.16-2.45;χ2 702.33)。由于MS DMTs可能影响MM的风险,临床医生应该教育PwMS定期皮肤自我检查的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malignant melanoma and multiple sclerosis therapies: A disproportionality analysis of the FDA adverse event reporting system.

Despite nationwide cohort studies revealing an increased risk of malignant melanoma (MM) in people with multiple sclerosis (PwMS), the connection between MS disease-modifying therapies (DMTs) and MM risk remains underexplored. We identified 1200 reports of MM associated with MS DMTs in the FDA Adverse Event Reporting System (FAERS), and a pooled analysis of all DMTs showed disproportionately high MM reporting compared to all other FAERS medications (reporting odds ratio, 2.30; 95% confidence interval, 2.16-2.45; χ2, 702.33). As MS DMTs may influence MM risk, clinicians should educate PwMS on the importance of regular skin self-examinations.

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