Department of Neurology, Military Institute of Medicine, Warsaw, Poland.
Department of Neurology, Poznan University of Medical Sciences, Poznan, Poland.
Neurol Neurochir Pol. 2023;57(4):371-378. doi: 10.5603/PJNNS.a2023.0050. Epub 2023 Jul 25.
Treatment with cladribine tablets is indicated in highly active relapsing-remitting multiple sclerosis (RRMS). Cladribine tablets proved safe and effective in the pivotal CLARITY trial, but that trial included primarily treatment-naïve patients. In clinical practice however, cladribine tablets are often given to patients who have failed other treatments. Therefore, this study investigated the real-world safety and efficacy of cladribine tablets.
We gathered data from nine MS clinical centres across Poland for patients with RRMS who started treatment with cladribine tablets from December 2019 to June 2022.
We enrolled 140 patients, with follow-up data available for 136 in year 1 and for 66 in year 2. At baseline, the mean age was 35.6 years, mean disease duration was 7.3 years, median EDSS score was 2.5, and 94% of patients were treatment- -experienced. Thirty-nine patients (27.9%) had undergone COVID-19, and 94 (67.1%) were vaccinated against COVID-19. The annualised relapse rate (ARR) decreased from 1.49 at baseline to 0.33 in year 1 (p < 0.001) and to 0.25 in year 2 (p < 0.001). The percentage of relapse-free patients increased from 11.5% at baseline to 70.2% in year 1 and 82.1% in year 2. The percentage of patients with active lesions decreased from 91.4% at baseline to 36.2% in year 1 and 18.2% in year 2. EDSS score remained stable or improved in 83.7% of patients in year 1 and 89.6% in year 2. No evidence of disease activity (NEDA-3) was achieved in 42.7% of patients in year 1 and 66.7% in year 2. Only one patient (0.72%) had grade 4 lymphopenia and 21 (15.1%) had grade 3 lymphopenia. Varicella zoster virus infections occurred in three patients. Eight patients discontinued treatment with cladribine: five due to inefficacy, one due to lymphopenia, and two due to a personal decision.
Cladribine tablets proved safe and effective in a real-world cohort of treatment-experienced patients. However, the efficacy measures improved to a lesser extent in our cohort than in the pivotal clinical trial, which is probably due to a higher proportion of treatment-experienced patients in our cohort.
克拉屈滨片在高度活跃的复发缓解型多发性硬化症(RRMS)中的治疗是有指征的。克拉屈滨片在关键的 CLARITY 试验中被证明是安全有效的,但该试验主要纳入了初治患者。然而,在临床实践中,克拉屈滨片通常用于已接受其他治疗但失败的患者。因此,本研究调查了克拉屈滨片的真实世界安全性和疗效。
我们从波兰的 9 个 MS 临床中心收集了 RRMS 患者的数据,这些患者于 2019 年 12 月至 2022 年 6 月开始接受克拉屈滨片治疗。
我们共纳入了 140 名患者,其中 136 名患者在第 1 年有随访数据,66 名患者在第 2 年有随访数据。基线时,患者平均年龄为 35.6 岁,平均病程为 7.3 年,EDSS 评分为 2.5,94%的患者有治疗经验。39 名患者(27.9%)发生过 COVID-19,94 名患者(67.1%)接种过 COVID-19 疫苗。年复发率(ARR)从基线时的 1.49 降至第 1 年的 0.33(p < 0.001)和第 2 年的 0.25(p < 0.001)。无复发患者的比例从基线时的 11.5%增加到第 1 年的 70.2%和第 2 年的 82.1%。有活动病灶的患者比例从基线时的 91.4%降至第 1 年的 36.2%和第 2 年的 18.2%。第 1 年和第 2 年,83.7%和 89.6%的患者的 EDSS 评分保持稳定或改善。第 1 年有 42.7%的患者和第 2 年有 66.7%的患者达到了无疾病活动(NEDA-3)的标准。只有 1 名患者(0.72%)出现 4 级淋巴细胞减少,21 名患者(15.1%)出现 3 级淋巴细胞减少。水痘带状疱疹病毒感染发生在 3 名患者中。8 名患者停止了克拉屈滨片的治疗:5 名患者因无效,1 名患者因淋巴细胞减少,2 名患者因个人决定。
克拉屈滨片在治疗经验丰富的患者的真实世界队列中证明是安全有效的。然而,与关键临床试验相比,我们队列中的疗效指标改善程度较小,这可能是由于我们队列中治疗经验丰富的患者比例较高。