Treatment of Multiple Sclerosis with Cladribine Tablets: Literature Review and the Guidance of the Lithuanian Association of Neurologists

R. Kizlaitienė, D. Mickevičienė, L. Malcienė, N. Giedraitienė, R. Balnytė, D. Jatužis
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Abstract

Cladribine is a disease-modifying drug used for the treatment of the highly active relapsing-remitting form of multiple sclerosis. Cladribine is a purine nucleoside analogue which selectively targets lymphocyte subpopulations involved in the pathogenesis of multiple sclerosis, and therefore it is classified as an immune reconstitution therapy drug. Two short courses of cladribine tablets given over two years significantly reduce the multiple sclerosis relapse rate and disability progression. For most patients, the effect persists in the third and the fourth year. This makes cladribine convenient for patients with multiple comorbidities, difficulties in adhering to their prescribed treatment regimen, those planning a pregnancy, or those for whom long-term immunosuppression is undesirable. Cladribine tablets are denoted by good safety characteristics, with the most prominent adverse effect being lymphopenia, which does not lead to an increased risk of infections other than Herpes zoster.However, in clinical practice, there are a number of issues related both to the initial administration of cladribine tablets and the strategy of treatment in different clinical situations during the first-to-fourth years of treatment, and particularly after the fourth year. Although there are no contraindications for additional courses of cladribine tablets, the product information does not provide detailed guidance on their continued use. During more than five years after the approval of the medicinal product, the new clinical trial data and the Real-World Evidence (RWE) on the efficacy and safety of cladribine tablets have become available, based on which, several national and international expert panels, as well as the Lithuanian Association of Neurologists, have issued guidance on the use of cladribine tablets reviewed in this article. Upon reactivation of the disease, additional courses of cladribine tablets or other disease-modifying therapies may be prescribed, depending on various factors related to the severity of the relapse, patient characteristics, and previously used medications. If the patient’s condition remains stable after the fourth year, extension of the treatment-free period with the structured monitoring approach could be appropriate.
克拉利宾片治疗多发性硬化症:文献综述和立陶宛神经病学家协会的指导意见
克拉利宾是一种改变病情的药物,用于治疗高度活跃的复发-缓解型多发性硬化症。克拉利宾是一种嘌呤核苷类似物,可选择性地靶向参与多发性硬化症发病机制的淋巴细胞亚群,因此被归类为免疫重建疗法药物。在两年内服用两个短期疗程的克拉德里滨片,可以明显降低多发性硬化症的复发率和残疾进展。对大多数患者来说,这种疗效在第三年和第四年仍会持续。因此,对于患有多种并发症、难以坚持处方治疗方案、计划怀孕或不希望长期接受免疫抑制治疗的患者来说,克拉利宾非常方便。克雷利宾片具有良好的安全性,最突出的不良反应是淋巴细胞减少,除带状疱疹外,不会导致感染风险增加。然而,在临床实践中,克雷利宾片的初始用药和治疗第一年至第四年,特别是第四年后不同临床情况下的治疗策略都存在一些问题。尽管克拉利宾片没有追加疗程的禁忌症,但产品信息并未对继续使用克拉利宾片提供详细指导。在该药品获得批准后的五年多时间里,有关克拉利宾片的疗效和安全性的新临床试验数据和真实世界证据(RWE)不断涌现,在此基础上,一些国家和国际专家小组以及立陶宛神经病学家协会发布了本文所回顾的克拉利宾片使用指南。当疾病再次复发时,可根据复发的严重程度、患者特征和先前使用的药物等各种因素,处方额外疗程的克拉利宾片或其他改变病情的疗法。如果患者的病情在第四年后保持稳定,可以适当延长无治疗期,并采用结构化监测方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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