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利妥昔单抗作为抗合成酶综合征相关间质性肺病的一线治疗药物。

Rituximab as the first-line therapy in anti-synthetase syndrome-related interstitial lung disease.

机构信息

Department of Rheumatology and Clinical Immunology, Faculty of Medicine, Clinical Hospital Center Rijeka, University of Rijeka, Rijeka, Croatia.

出版信息

Rheumatol Int. 2023 Jun;43(6):1015-1021. doi: 10.1007/s00296-023-05302-9. Epub 2023 Mar 16.

Abstract

Anti-synthetase syndrome (ASS) is an idiopathic inflammatory myopathy (IIM). In comparison to interstitial lung disease (ILD) in polymyositis and dermatomyositis (PM/DM), ILD in ASS is more frequent, has a more aggressive phenotype, a greater involvement of the lungs, and a more rapid onset of pulmonary symptoms. Continuous declines in predicted forced vital capacity (FVC) and dyspnea were the main features of patients who developed end-stage ILD. The severity of ASS at diagnosis dictates when and which immunosuppressant will be started. There is an experience for the usage of RTX in the first, second, and subsequent lines, as well as for reintroduction and salvage therapies. Not all ASS patients will develop severe illness and require intense immunosuppression. Some features associated with poor prognosis include older age, acute or subacute onset, lack of response to steroids, and lower baseline values for FVC and DLCO. Here we hypothesize that RTX should be the first line of treatment for high-risk ILD in ASS to preserve lung function and then maintenance therapy should be continued with the same or another drug depending on the recovery of lung function.

摘要

抗合成酶综合征 (ASS) 是一种特发性炎症性肌病 (IIM)。与多发性肌炎和皮肌炎 (PM/DM) 中的间质性肺病 (ILD) 相比,ASS 中的 ILD 更为常见,具有更具侵袭性的表型,更广泛的肺部受累和更快速的肺部症状发作。预测用力肺活量 (FVC) 和呼吸困难持续下降是发展为终末期 ILD 的患者的主要特征。ASS 诊断时的严重程度决定了何时以及使用哪种免疫抑制剂开始治疗。RTX 在一线、二线和后续线以及重新引入和挽救治疗中都有使用经验。并非所有 ASS 患者都会出现严重疾病并需要强烈的免疫抑制治疗。一些与预后不良相关的特征包括年龄较大、急性或亚急性发作、对类固醇无反应以及 FVC 和 DLCO 的基线值较低。在这里,我们假设 RTX 应该是 ASS 高危 ILD 的一线治疗药物,以保留肺功能,然后根据肺功能的恢复继续使用相同或另一种药物进行维持治疗。

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