Meuth S G, Ruck T, Aktas O, Hartung H-P
Klinik für Neurologie mit Institut für Translationale Neurologie, Universitätsklinikum Münster, Albert-Schweitzer-Campus 1, Gebäude A1, Westturm, Ebene 05, 48149, Münster, Deutschland.
Klinik für Neurologie, Universitätsklinikum Düsseldorf, Heinrich-Heine-Universität, Düsseldorf, Deutschland.
Nervenarzt. 2018 Aug;89(8):895-907. doi: 10.1007/s00115-018-0498-0.
The selective modulation of lymphocyte numbers and function is an attractive concept in the treatment of relapsing-remitting multiple sclerosis (RMS).
Cladribine tablets (Mavenclad®), an oral RMS medication with an innovative treatment concept, have been available since August 2017. This review article summarizes the currently available clinical study data on cladribine tablets and aspects of their use in clinical practice.
Cladribine tablets are administered during two treatment phases of 8-10 (two times 4-5) days with a 1-year interval. The drug selectively reduces the number of T and B lymphocytes, which are subsequently gradually reconstituted with divergent kinetics. A pronounced and sustained effect on the clinical and paraclinical MS disease activity is achieved with good tolerability and a favorable overall safety profile. After completing the two short treatment phases, a relevant proportion of the treated patients experience a prolonged treatment-free period with absence of relevant disease activity. Regular monitoring of lymphocyte counts and reliable contraception during the required time frames are the most important safety measures. There is no evidence of an increased risk of malignancies.
Cladribine tablets are an important addition to the therapeutic landscape in RMS. With patient-friendly short dosing periods and a favorable adverse event profile, cladribine tablets provide a sustained and strong reduction of MS disease activity. The primary target population for cladribine tablets is patients with relevant MS disease activity (highly active RMS) while on first-line treatment, e. g. with injectable disease-modifying drugs.
选择性调节淋巴细胞数量和功能是复发缓解型多发性硬化症(RMS)治疗中一个有吸引力的概念。
克拉屈滨片(Mavenclad®)是一种具有创新治疗理念的口服RMS药物,自2017年8月起可用。这篇综述文章总结了目前关于克拉屈滨片的临床研究数据及其在临床实践中的应用情况。
克拉屈滨片在两个为期8 - 10天(两次4 - 5天)的治疗阶段给药,间隔1年。该药物选择性减少T和B淋巴细胞数量,随后这些细胞以不同的动力学逐渐重建。对临床和临床旁多发性硬化症疾病活动有显著且持续的效果,耐受性良好,总体安全性良好。在完成两个短治疗阶段后,相当比例的接受治疗的患者经历了无相关疾病活动的延长的无治疗期。在规定时间内定期监测淋巴细胞计数和可靠避孕是最重要的安全措施。没有证据表明患恶性肿瘤的风险增加。
克拉屈滨片是RMS治疗领域的一项重要补充。克拉屈滨片给药期短,对患者友好,不良事件谱良好,能持续且显著降低MS疾病活动。克拉屈滨片的主要目标人群是一线治疗时患有相关MS疾病活动(高度活跃的RMS)的患者,例如使用注射用疾病修正药物治疗的患者。