免疫抑制治疗弥漫性皮肤系统性硬化症的比较疗效。

IF 2.8 Q2 RHEUMATOLOGY
Barbara White, Daniel E Furst, Tracy M Frech, Masataka Kuwana, Laura Hummers, Wendy Stevens, Suzanne Kafaja, Eun Bong Lee, Oliver Distler, Dinesh Khanna, Christopher P Denton, Robert Spiera
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引用次数: 0

摘要

目的:lenabasum在弥漫性皮肤系统性硬化症(dcSSc)中的RESOLVE-1试验允许个体研究者自行决定本底免疫抑制治疗(IST),治疗组之间没有观察到显著差异。这提供了一个强大的机会来比较不同ist在一个明确的大队列dcSSc患者中的相对疗效。方法:预先指定的IST类别、疗效终点、可能影响疗效结果的基线疾病特征、间质性肺疾病的定义、IST使用的定义以及评估疗效结果的IST使用类别。描述性统计用于显示结果。结果:对于皮肤,在发病最早的患者中,霉酚酸酯(MMF)治疗后,改良罗德曼皮肤评分(mRSS)的变化在数值上最大,在病程≤2年的患者中,MMF组达到-10.8分,而非IST组为-4.8分。其他IST组的改善介于MMF组和无IST组之间。MMF组患者的用力肺活量(mL)在52周内保持稳定,而非IST组患者的用力肺活量在52周内下降约160 mL。在抗核抗体亚组之间观察到结果的差异,在抗拓扑异构酶1自身抗体阳性的患者中观察到MMF对皮肤和肺部的影响差异更大。相比之下,抗rna聚合酶III自身抗体阳性的患者在没有IST和MMF组中都迅速改善,mRSS下降。结论:综上所述,我们的研究结果有力地支持在dcSSc中常规使用MMF,并显示出对早期疾病的益处。那些有肺纤维化高危抗体的患者可能特别适合MMF治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative Efficacy of Immunosuppressive Therapies in the Treatment of Diffuse Cutaneous Systemic Sclerosis.

Comparative Efficacy of Immunosuppressive Therapies in the Treatment of Diffuse Cutaneous Systemic Sclerosis.

Comparative Efficacy of Immunosuppressive Therapies in the Treatment of Diffuse Cutaneous Systemic Sclerosis.

Comparative Efficacy of Immunosuppressive Therapies in the Treatment of Diffuse Cutaneous Systemic Sclerosis.

Objectives: The RESOLVE-1 trial of lenabasum in diffuse cutaneous systemic sclerosis (dcSSc) allowed background immunosuppressive therapy (IST) at the discretion of individual investigators, and no significant differences were observed between treatment arms. This provides a powerful opportunity to compare the relative efficacy of different ISTs in a well-defined large cohort of patients with dcSSc.

Methods: Prespecified IST categories, efficacy end points, baseline disease characteristics likely to influence efficacy outcomes, the definition of interstitial lung disease, definitions of IST use, and categories of IST use by which efficacy outcomes were evaluated were. Descriptive statistics are used to present results.

Results: For skin, change in modified Rodnan skin score (mRSS) was numerically greatest with mycophenolate mofetil (MMF) treatment in patients with the earliest disease, reaching -10.8 points in the MMF group versus -4.8 points in the no IST group in patients with a disease duration ≤2 years. Other ISTs had improvements intermediate between that seen in the MMF and no IST groups. Forced vital capacity (mL) was stable over 52 weeks in patients in the MMF group compared to an around 160-mL decline over 52 weeks in no IST group. Differences in outcome were observed between antinuclear antibody subgroups, with greater difference in favor of MMF for skin and lungs being observed in anti-topoisomerase 1 autoantibody-positive patients. In contrast, anti-RNA polymerase III autoantibody-positive patients in both the no IST and MMF groups improved rapidly, with a decrease in mRSS.

Conclusion: Taken together, our findings robustly support routine use of MMF in dcSSc and show benefit especially in early-stage disease. Those patients with high-risk antibodies for lung fibrosis might be especially suitable for MMF treatment.

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来源期刊
CiteScore
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