Guerra Tommaso, Copetti Massimiliano, Zanetta Chiara, Patti Francesco, Chisari Clara Grazia, Barbuti Elena, Portaccio Emilio, Foschi Matteo, Conte Antonella, Ferraro Diana, Cocco Eleonora E, Fantozzi Roberta, Maniscalco Giorgia Teresa, Salemi Giuseppe, Tortorella Carla, Paolicelli Damiano, Filippi Massimo, Amato Maria Pia, Trojano Maria, Iaffaldano Pietro
Department of Translational Biomedicine and Neurosciences, University of Bari "Aldo Moro", Italy.
Unit of Biostatistics, Fondazione IRCCS -"Casa Sollievo della Sofferenza", San Giovanni Rotondo, Italy.
Neurol Neuroimmunol Neuroinflamm. 2025 Jul;12(4):e200415. doi: 10.1212/NXI.0000000000200415. Epub 2025 Jun 5.
Cladribine is an immune reconstitution therapy approved for relapsing multiple sclerosis (RMS). This multicentric retrospective study of the Italian Multiple Sclerosis Register (RISM) aimed to assess the effect of cladribine on the annualized relapse rate (ARR) and progression independent of relapse activity (PIRA) phenomena, also evaluating the strategies of disease-modifying treatment (DMT) continuation after cladribine termination.
Patients with RMS treated with at least one cycle of cladribine recorded in RISM after 2018 were retrospectively included in the analysis. Patients previously treated with other DMTs were stratified into moderately and highly effective DMTs. Adjusted ARR and PIRA events were calculated in the overall cohort and stratified by age at cladribine start (<50 vs ≥ 50 years) and by previous DMT. ARRs were compared between groups using negative binomial models. PIRA was analyzed using the Ghosh-Lin Cox-type regression for the marginal mean. DMTs prescribed after cladribine cycles were analyzed.
A total of 2,329 patients treated with cladribine were identified in RISM, with a median (IQR) age of 36.5 (29.2-45.2) years at treatment start. 1,488 patients (63.9%) received 2 courses of cladribine. ARR decreased ( < 0.0001) from 0.96 (95% CI 0.91-1.02) in the 2 years preceding cladribine start to 0.09 (0.08-0.11) during the 2 years after in the overall cohort. One hundred thirty-three PIRA events were reported during the noncladribine treatment period and 54 during cladribine therapy (HR 0.711, 95% CI 0.531-0.952, = 0.0219) in the entire cohort. All the analyses stratified by age and previous treatment confirmed the significant reduction in PIRA events and the suppression of relapse activity. After cladribine, most DMTs prescribed were ocrelizumab, ofatumumab, and natalizumab. Eight patients re-treated with an additional cycle of cladribine were also identified.
For patients with RMS, both naïve and switchers, as well as younger and older patients, cladribine is an effective treatment in reducing relapses and PIRA. Different therapeutic strategies after cladribine are currently reported.
This study provides Class IV evidence that for patients with relapsing multiple sclerosis, cladribine treatment is associated with a reduction in ARR and PIRA events.
克拉屈滨是一种被批准用于复发型多发性硬化症(RMS)的免疫重建疗法。这项对意大利多发性硬化症注册库(RISM)进行的多中心回顾性研究旨在评估克拉屈滨对年化复发率(ARR)和独立于复发活动的疾病进展(PIRA)现象的影响,同时评估克拉屈滨停药后疾病修饰治疗(DMT)的延续策略。
回顾性纳入2018年后在RISM中记录的接受至少一个周期克拉屈滨治疗的RMS患者进行分析。先前接受过其他DMT治疗的患者被分为中度和高度有效的DMT组。在整个队列中计算调整后的ARR和PIRA事件,并根据开始使用克拉屈滨时的年龄(<50岁与≥50岁)和先前的DMT进行分层。使用负二项模型比较各组之间的ARR。使用Ghosh-Lin Cox型边际均值回归分析PIRA。分析克拉屈滨治疗周期后开具的DMT。
在RISM中确定了总共2329例接受克拉屈滨治疗的患者,治疗开始时的中位(IQR)年龄为36.5(29.2-45.2)岁。1488例患者(63.9%)接受了2个疗程的克拉屈滨治疗。在整个队列中,ARR从开始使用克拉屈滨前2年的0.96(95%CI 0.91-1.02)降至开始使用克拉屈滨后2年的0.09(0.08-0.11)(<0.0001)。在整个队列的非克拉屈滨治疗期间报告了133例PIRA事件,在克拉屈滨治疗期间报告了54例(HR 0.711,95%CI 0.531-0.952,=0.0219)。所有按年龄和先前治疗分层的分析均证实PIRA事件显著减少且复发活动得到抑制。克拉屈滨治疗后,开具的大多数DMT是奥瑞珠单抗、奥法木单抗和那他珠单抗。还确定了8例再次接受一个周期克拉屈滨治疗的患者。
对于初治和换药治疗的RMS患者,以及年轻和老年患者,克拉屈滨在减少复发和PIRA方面是一种有效的治疗方法。目前报道了克拉屈滨治疗后的不同治疗策略。
本研究提供了IV类证据,即对于复发型多发性硬化症患者,克拉屈滨治疗与ARR和PIRA事件的减少相关。