Conticini Edoardo, Cameli Paolo, Grazzini Silvia, d'Alessandro Miriana, Bergantini Laura, Porcelli Brunetta, Mazzei Maria Antonietta, Cantarini Luca, Bargagli Elena, Frediani Bruno
Rheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Italy.
Respiratory Diseases Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Italy.
Semin Arthritis Rheum. 2024 Dec;69:152560. doi: 10.1016/j.semarthrit.2024.152560. Epub 2024 Sep 24.
Anti-synthetase syndrome (ASS) is a rare autoimmune disease characterized by the presence of anti-aminoacyl-transfer-RNA synthetase antibodies (ARS) and the involvement of muscles, skin, joints, and lungs. Despite increasing interest and evidence, optimal clinical management remains unclear due to a lack of randomized control trials. This study aims to evaluate the efficacy and safety of a treatment regimen involving early co-administration of glucocorticoids and immunosuppressants, with rapid prednisone tapering.
We prospectively enrolled patients referred to our multidisciplinary "Myositis Clinic" with a diagnosis of ASS. Clinical, serological, instrumental and medications data were collected at baseline and at 6 and 12 months follow-up. According to treatment protocol, patients were treated with traditional synthetic immunosuppressants or rituximab (RTX) depending on clinical manifestations. Prednisone (PDN) was gradually tapered and eventually discontinued within 6 or 12 months.
A total of twenty-seven subjects were enrolled: arthritis, myositis and ILD were assessed in 9, 16 and 18 patients, respectively, and all of them had an active disease. RTX was administered after methotrexate (MTX) in 4 cases of refractory joint involvement and co-administration of a second immunosuppressant was necessary in 2 patients. When muscle involvement was present, first-line therapy was MTX, followed by mycophenolate mofetil (MMF) or RTX, which allowed to achieve low disease activity or remission, respectively. Eight ILD-patients were treated with MMF and switched to RTX in 5 cases of inefficacy, but all patients were in clinical remission at the end of follow-up. At 12 months, 12 patients discontinued PDN.
This study is the first to prospectively report on the efficacy and safety of a stepwise, steroid-sparing treatment ASS encompassing various domains. MTX, as well as other synthetic immunosuppressants, showed limited efficacy in ASS-related arthritis, while RTX emerged as a promising option. This study recommends early RTX use in case of arthritis, suggesting it as a pivotal treatment for ILD too, and raises questions regarding maintenance therapy and treatment-free remission.
抗合成酶综合征(ASS)是一种罕见的自身免疫性疾病,其特征为存在抗氨酰 - 转移RNA合成酶抗体(ARS),并累及肌肉、皮肤、关节和肺部。尽管对此的关注度和相关证据不断增加,但由于缺乏随机对照试验,最佳临床管理仍不明确。本研究旨在评估早期联合使用糖皮质激素和免疫抑制剂并快速减量泼尼松的治疗方案的疗效和安全性。
我们前瞻性地纳入了被转诊至我们多学科“肌炎诊所”且诊断为ASS的患者。在基线以及随访6个月和12个月时收集临床、血清学、影像学和用药数据。根据治疗方案,根据临床表现,患者接受传统合成免疫抑制剂或利妥昔单抗(RTX)治疗。泼尼松(PDN)逐渐减量,并最终在6个月或12个月内停用。
共纳入27名受试者:分别对9例、16例和18例患者评估了关节炎、肌炎和间质性肺病(ILD),且所有患者均患有活动性疾病。4例难治性关节受累患者在甲氨蝶呤(MTX)之后使用了RTX,2例患者需要联合使用第二种免疫抑制剂。当存在肌肉受累时,一线治疗为MTX,随后使用霉酚酸酯(MMF)或RTX,分别使疾病达到低活动度或缓解。8例ILD患者接受MMF治疗,5例无效后改用RTX,但所有患者在随访结束时均处于临床缓解状态。在12个月时,12例患者停用了PDN。
本研究首次前瞻性地报告了一种涵盖各个领域的逐步减少激素用量治疗ASS的疗效和安全性。MTX以及其他合成免疫抑制剂在ASS相关关节炎中显示出有限的疗效,而RTX成为一种有前景的选择。本研究建议在关节炎情况下早期使用RTX,也表明其对ILD是关键治疗方法,并引发了关于维持治疗和无治疗缓解的问题。