Centre de ressources et compétences SEP, neurologie, université Nice-Côte-d'Azur, CHU Pasteur 2, 30, voie Romaine, 06002 Nice, France.
Centre de ressources et compétences SEP, neurologie, université Nice-Côte-d'Azur, CHU Pasteur 2, 30, voie Romaine, 06002 Nice, France.
Rev Neurol (Paris). 2018 Dec;174(10):722-725. doi: 10.1016/j.neurol.2017.11.010. Epub 2018 Nov 5.
Teriflunomide, a novel, orally bioavailable, active metabolite of leflunomide, has anti-inflammatory activity. It is prescribed as a first-line treatment for relapsing-remitting multiple sclerosis (RRMS) at a dose of one 14mg tablet per day. Common adverse reactions observed in placebo-controlled trials with a frequency≥10% and a rate twofold or more than reported with placebo, include digestive disorders. As teriflunomide tablets also contain lactose, the official recommendations are clear about not prescribing this drug to patients with known lactose intolerance and those with rare hereditary problems due to galactose intolerance.
Our study systematically collected, from our MS clinical practice, all adverse events presenting in the first 100 patients treated with teriflunomide. All of these patients were systematically asked if they were known to have lactose intolerance.
None of these 100 patients declared having known, documented lactose intolerance. Yet, after starting teriflunomide, 14 reported mild-to-moderate diarrhea, which resolved within a month, but four of these patients continued to have daily diarrhea (grade 2 WHO classification), prompting us to perform a lactose breath test (LBT) for malabsorption. All four tested positive and were therefore diagnosed with lactose intolerance. Digestive symptoms were resolved with probiotics, and teriflunomide was maintained in three cases; the fourth patient decided, despite the adverse event being resolved, to stop taking teriflunomide.
In cases of prolonged digestive side-effects after the introduction of teriflunomide, a lactose-malabsorption breath test should be proposed to confirm the culpability or not of an enzymatic defect in the occurrence of adverse events.
特立氟胺是一种新型、口服生物利用度高的来氟米特活性代谢物,具有抗炎活性。它被规定为每天一次,每次 14mg 片剂,作为复发缓解型多发性硬化症(RRMS)的一线治疗药物。在安慰剂对照试验中,常见的不良反应发生率≥10%,且频率是安慰剂的两倍或更高,包括消化系统疾病。由于特立氟胺片剂还含有乳糖,因此官方建议对于已知乳糖不耐受的患者和由于半乳糖不耐受而患有罕见遗传性疾病的患者,不使用该药。
我们的研究系统地从我们的多发性硬化症临床实践中收集了接受特立氟胺治疗的前 100 名患者出现的所有不良事件。我们系统地询问了所有这些患者是否已知患有乳糖不耐受。
这 100 名患者均未声明已知的、有记录的乳糖不耐受。然而,在开始使用特立氟胺后,有 14 名患者出现轻度至中度腹泻,在一个月内得到缓解,但其中 4 名患者仍持续每日腹泻(世界卫生组织 2 级分类),这促使我们进行乳糖呼气试验(LBT)以检测吸收不良。这 4 名患者均检测出阳性,因此被诊断为乳糖不耐受。通过益生菌治疗,消化症状得到缓解,在 3 例中继续使用特立氟胺,而第 4 例患者尽管不良反应已得到解决,但仍决定停止使用特立氟胺。
在使用特立氟胺后出现长时间的消化系统副作用时,应提出乳糖吸收不良呼气试验以确认不良事件是否因酶缺陷引起。