巨细胞动脉炎免疫抑制剂和生物制剂的使用:法国大血管炎研究小组(GEFA)的建议。

Hubert de Boysson, Valérie Devauchelle-Pensec, Christian Agard, Marc André, Boris Bienvenu, Bernard Bonnotte, Guillermo Carvajal Alegria, Olivier Espitia, Eric Hachulla, Emmanuel Héron, Marc Lambert, Jean-Christophe Lega, Kim H Ly, Arsène Mekinian, Jacques Morel, Alexis Régent, Christophe Richez, Laurent Sailler, Raphaele Seror, Anne Tournadre, Maxime Samson
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引用次数: 0

摘要

目的:需要对法国大血管炎研究小组(GEFA)2016 年的建议进行更新修订,以更好地界定免疫抑制剂或生物制剂在巨细胞动脉炎(GCA)中的地位和管理:由包括内科医生和风湿病学家在内的 18 名医生组成了该项目的工作组,并起草了建议。另外还邀请了 12 位读者对建议进行分析和评论。召开了两次面对面的虚拟会议来讨论和验证建议。每位成员都进行了单独投票,85%以上的成员达成共识才能确认每项建议:结果:从最初的 6 个问题中,有 26 项建议得到了验证。以下主要建议得到了验证。(1)如果需要使用糖皮质激素(GC)替代治疗,应首先使用皮下注射 162 毫克托西珠单抗(TCZ),疗程至少 12 个月,目标是在随后的 6 个月内停用 GC。(2)GCA患者如出现以下任何一种情况,必须在确诊GCA时接受TCZ治疗,并接受6个月的GC治疗:重大心血管事件、骨质疏松症伴骨折、使用GC时出现精神病事件、复杂性糖尿病或既往接受过超过6个月的GC治疗。(3)对于因疾病持续活动而无法在治疗 12 个月后停用 GC 的患者,或无法接受 GC 相关不良事件的患者,可建议使用 TCZ(或甲氨蝶呤):这些建议是根据已发表文献的结果和专家的经验提出的,旨在规范法国的治疗实践。在有新的文献发表后,可能需要进一步更新。
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Use of immunosuppressants and biologics in giant cell arteritis: Recommendations of the French Study Group for Large Vessel Vasculitis (GEFA).

Purpose: An updated revision of the 2016 recommendations from the French Study Group for Large Vessel Vasculitis (GEFA) was needed to better delineate the place and management of immunosuppressants or biologics in giant cell arteritis (GCA).

Methods: A panel of 18 physicians, including internists and rheumatologists, constituted the task force of this project and drafted the recommendations. Twelve additional readers were asked to analyse and comment on the recommendations. Two face-to-face virtual meetings were held to discuss and validate the recommendations. Each member voted individually, and a>85% consensus was required to validate each recommendation.

Results: From the initial 6 questions, 26 recommendations were validated. The following main recommendations were validated. (1) Subcutaneous 162mg tocilizumab (TCZ) for at least 12months should be used first when glucocorticoid (GC)-sparing treatment is needed with the objective of discontinuing GCs within the subsequent 6months. (2) GCA patients who have experienced any of the following conditions must receive TCZ at GCA diagnosis with 6months of GC therapy: major cardiovascular event, osteoporosis with fracture, psychiatric event with GC use, complicated diabetes mellitus, or any previous>6months of GC treatment. (3) In patients in whom GC discontinuation is not possible after 12months of treatment because of persistent disease activity or in patients in whom GC-related adverse events are unacceptable, TCZ (or alternatively methotrexate) may be proposed.

Conclusions: These recommendations were constructed based on the results of the published literature and the experts' experiences to standardise therapeutic practices in France. Further updates will likely be necessary following new publications.

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