Qiu Li, Chen Pei, Ou Changyi, Deng Juan, Huang Zhidong, Lin Zhongqiang, Ma Qian, Huang Xin, Yu Lu, Ran Hao, Liu Weibin
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases, Guangzhou, China.
Acta Neurol Belg. 2024 Feb;124(1):175-182. doi: 10.1007/s13760-023-02367-y. Epub 2023 Sep 1.
Leflunomide and low-dose prednisone (0.25 mg/kg/day) (LEF + Pred) rapidly improved the clinical symptoms of myasthenia gravis (MG) patients. Here, we aimed to analyze the long-term efficacy and safety of LEF + Pred in MG patients.
This retrospective cohort study enrolled MG patients treated with LEF + Pred in our center between 2012 and 2020. We reviewed all the MG patients continuously treated with LEF + Pred for more than 1 year. MG activities of daily living (MG-ADL) profile score and quantitative MG scale (QMG) score in each clinical follow-up visits were collected for the efficacy analysis. The laboratory testing results of MG patients, the relevant chief complain and physical examination results in each follow-up visits were collected for the safety evaluation.
In total, 103 patients were examined. Effective treatment was achieved in 58.3% of patients after 1 month and in 88.4% after 12 months. Overall, 63 patients (61.2%) exhibited only minimal manifestations after 12 months of treatment. The average MG-ADL score decreased from 6.0 to 1.0, while the average QMG score decreased from 10.0 to 4.0. The decrease in MG-ADL and QMG scores of patients with generalized MG was more pronounced than those of the ocular MG patients. Patients with MG who had a thymectomy had a smaller decrease in MG-ADL and QMG scores than those who did not have a thymectomy. Sixteen adverse effects associated with LEF + Pred were observed; none was severe.
Long-term LEF + Pred therapy could considerably improve clinical symptoms in MG patients while being well tolerated with just few side effects.
来氟米特与低剂量泼尼松(0.25毫克/千克/天)(LEF+Pred)能迅速改善重症肌无力(MG)患者的临床症状。在此,我们旨在分析LEF+Pred治疗MG患者的长期疗效和安全性。
这项回顾性队列研究纳入了2012年至2020年期间在我们中心接受LEF+Pred治疗的MG患者。我们对所有持续接受LEF+Pred治疗超过1年的MG患者进行了回顾。收集每次临床随访时MG日常生活活动(MG-ADL)概况评分和定量MG量表(QMG)评分以进行疗效分析。收集MG患者的实验室检测结果、每次随访时的相关主诉和体格检查结果以进行安全性评估。
总共检查了103例患者。1个月后58.3%的患者获得有效治疗,12个月后为88.4%。总体而言,63例患者(61.2%)在治疗12个月后仅表现出轻微症状。MG-ADL平均评分从6.0降至1.0,而QMG平均评分从10.0降至4.0。全身型MG患者的MG-ADL和QMG评分下降比眼肌型MG患者更明显。接受胸腺切除术的MG患者的MG-ADL和QMG评分下降幅度小于未接受胸腺切除术的患者。观察到16例与LEF+Pred相关的不良反应;均不严重。
长期LEF+Pred治疗可显著改善MG患者的临床症状,且耐受性良好,副作用较少。