Jamroz-Wiśniewska Anna, Zajdel Radosław, Słowik Agnieszka, Marona Monika, Wnuk Marcin, Adamczyk-Sowa Monika, Adamczyk Bożena, Lasek-Bal Anetta, Puz Przemysław, Stęposz Arkadiusz, Krzystanek Ewa, Patalong-Ogiewa Maja, Pokryszko-Dragan Anna, Budrewicz Sławomir, Koziarska Dorota, Karbicka Anna, Wawrzyniak Sławomir, Fryze Waldemar, Furtak-Niczyporuk Marzena, Rejdak Konrad
Department of Neurology, Medical University of Lublin, Jaczewskiego 8, 20-054 Lublin, Poland.
Chair of Informatics in Business, University of Lodz, Rewolucji 1905 Roku 37/39, 91-001 Lodz, Poland.
J Clin Med. 2021 Apr 22;10(9):1830. doi: 10.3390/jcm10091830.
Reliable markers of disease outcomes in multiple sclerosis (MS) would help to predict the response to treatment in patients treated with high efficacy drugs. No evidence of disease activity (NEDA) has become a treatment goal whereas the modified Rio score (MRS) predicts future suboptimal responders to treatment. The aim of our study was to identify factors that would predict poor response to treatment with natalizumab and fingolimod.
In the multicenter prospective trial, 336 subjects were enrolled, initiating therapy with natalizumab ( = 135) or fingolimod ( = 201). Data on relapse rate, the expanded disability status scale, and MRI results were collected, and MRS was estimated.
NEDA-3 after the first year of therapy was 73.9% for natalizumab and 54.8% for fingolimod ( < 0.0001). Patients with MRS = 0 in the last year on platform therapy had the best NEDA-3 (71%) and patients with MRS = 3 had the worst NEDA-3 (41%) in the first year of treatment with the second-line therapy.
We conclude that switching to the second-line therapy should occur earlier to enable better results for patients treated with natalizumab or fingolimod. The outcome on both drugs is better with better neurological conditions and lower MRS of the patient on the platform therapy.
多发性硬化症(MS)疾病转归的可靠标志物有助于预测接受高效药物治疗患者的治疗反应。无疾病活动证据(NEDA)已成为一个治疗目标,而改良里约评分(MRS)可预测未来治疗反应欠佳的患者。我们研究的目的是确定可预测那他珠单抗和芬戈莫德治疗反应不佳的因素。
在这项多中心前瞻性试验中,招募了336名受试者,开始使用那他珠单抗(n = 135)或芬戈莫德(n = 201)进行治疗。收集了复发率、扩展残疾状态量表和MRI结果的数据,并估算了MRS。
治疗第一年的NEDA-3,那他珠单抗组为73.9%,芬戈莫德组为54.8%(P < 0.0001)。在二线治疗的第一年,平台治疗最后一年MRS = 0的患者NEDA-3最佳(71%),而MRS = 3的患者NEDA-3最差(41%)。
我们得出结论,应更早地切换到二线治疗,以使接受那他珠单抗或芬戈莫德治疗的患者获得更好的结果。在平台治疗中,患者神经状况越好且MRS越低,两种药物的治疗效果越好。