Imai Tomihiro, Suzuki Shigeaki, Nagane Yuriko, Uzawa Akiyuki, Murai Hiroyuki, Utsugisawa Kimiaki
Department of Neurology, Sapporo Medical University Hospital, Sapporo, Japan.
Department of Neurology, Keio University School of Medicine, Tokyo, Japan.
Front Neurol. 2020 Aug 25;11:868. doi: 10.3389/fneur.2020.00868. eCollection 2020.
Treatment with oral corticosteroids at high doses with an escalation and de-escalation schedule is effective against myasthena gravis (MG). In fact, the use of corticosteroids has led to a reduction in mortality to below 10% after the 1960s. However, long-term use of oral steroids above a certain dosage level is known to cause a number of problems. In 2014, the Japanese clinical guidelines for MG proposed that the first goal in MG treatment (treatment target) should be set at minimal manifestations (MM) with oral prednisolone (PSL) 5 mg/day or below, and that treatment strategies should strive to attain this level as rapidly as possible. In 2015, a multicenter, cross-sectional study revealed that higher PSL dose and longer PSL treatment do not ensure better outcome. In the absence of good response, the PSL dose should be decreased by combining with modalities such as plasma exchange/plasmapheresis and intravenous immunoglobulin (fast-acting treatments). In 2018, we conducted a multicenter, cross-sectional study in a large population of Japanese patients with generalized MG, aiming to elucidate the correlation between oral PSL regimens and achievement of treatment goals. The ORs for low vs. high dose to achieve treatment goals at 1, 2, and 3 years were 10.4, 2.75, and 1.86, respectively, whereas the corresponding ORs for low vs. medium dose were 13.4, 3.99, and 4.92. Early combination with fast-acting therapy (OR 2.19 at 2 years, 2.11 at 3 years) or combination with calcineurin inhibitors (OR 2.09 at 2 years, 2.36 at 3 years) were also positively associated with achieving treatment goals. These results indicate that early combination of low-dose PSL regimens with other therapies is the key for early achievement of treatment goals in generalized MG. However, even with this regimen, ~35% of patients did not achieve the treatment target after 3 years. These results suggest the limitation of the current oral corticosteroid therapy. We need to develop new treatment options to increase the rate of satisfactory outcome.
采用高剂量口服皮质类固醇并结合递增和递减方案治疗重症肌无力(MG)是有效的。事实上,自20世纪60年代以来,皮质类固醇的使用已使死亡率降至10%以下。然而,长期使用超过一定剂量水平的口服类固醇会引发诸多问题。2014年,日本MG临床指南提出,MG治疗的首要目标(治疗靶点)应设定为口服泼尼松龙(PSL)5毫克/天及以下时的最小症状(MM),且治疗策略应努力尽快达到这一水平。2015年,一项多中心横断面研究表明,较高的PSL剂量和较长的PSL治疗时间并不能确保更好的疗效。若反应不佳,应通过联合血浆置换/血浆去除术和静脉注射免疫球蛋白等方式(快速起效治疗)来降低PSL剂量。2018年,我们对大量日本全身性MG患者进行了一项多中心横断面研究,旨在阐明口服PSL方案与治疗目标达成之间的相关性。低剂量与高剂量在1年、2年和3年达到治疗目标的比值比(OR)分别为10.4、2.75和1.86,而低剂量与中等剂量的相应OR分别为13.4、3.99和4.92。早期联合快速起效治疗(2年时OR为2.19,3年时为2.11)或联合钙调神经磷酸酶抑制剂(2年时OR为2.09,3年时为2.36)也与实现治疗目标呈正相关。这些结果表明,低剂量PSL方案与其他疗法的早期联合是全身性MG早期实现治疗目标的关键。然而,即便采用这种方案,仍有约35%的患者在3年后未达到治疗靶点。这些结果提示了当前口服皮质类固醇疗法的局限性。我们需要开发新的治疗方案以提高满意疗效的比例。