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Glukokortikoide in der Therapie der Riesenzellarteriitis

Wie viel und wie lange und womit einsparen?

Glucocorticoids in the treatment of giant cell arteritis

How much, how long and how to spare?

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Zeitschrift für Rheumatologie Aims and scope Submit manuscript

Zusammenfassung

Eine Therapie einer Riesenzellarteriitis (RZA) mit hoch dosierten Glukokortikoiden (GC) führt regelhaft zu einer Kontrolle der entzündlichen Aktivität, sodass hoch dosierte GC in den aktuellen Leitlinien weiterhin als Therapiestandard empfohlen werden. Allerdings kommt es nach Beendigung der GC-Therapie bzw. Reduktion der GC-Dosis bei bis zu 70 % der Patienten im weiteren Krankheitsverlauf zu Rezidiven, die eine Wiederaufnahme der Therapie bzw. eine Dosiserhöhung erforderlich machen. In der Konsequenz müssen daher viele Patienten über mehrere Jahre mit teils höher dosierten GC behandelt werden, was eine hohe kumulative GC-Exposition zur Folge hat. Das Risiko für GC-assoziierte Erkrankungen wie Diabetes, Glaukom, Osteoporose oder schwere Infektion ist daher für Patienten mit einer Riesenzellarteriitis deutlich erhöht. Für Patienten mit GC-assoziierten Komorbiditäten bzw. erhöhtem Risiko, diese zu entwickeln, oder Patienten mit einem Rezidiv empfehlen aktuelle Leitlinien daher eine GC-sparende Therapie mit Tocilizumab oder alternativ Methotrexat. Unklar ist derzeit, über welchen Zeitraum Patienten mit einer RZA mit GC und auch GC-sparenden Therapien behandelt werden sollten, da hochwertige Studiendaten zu Deeskalationsstrategien für die RZA derzeit noch fehlen. Entscheidungen zu Therapiedauer und -intensität müssen daher patientenindividuell unter Abwägung von allgemeinen und patientenspezifischen Risikofaktoren für einen GC-abhängigen Verlauf, RZA-assoziierten Gefäßschäden (Stenosen, Aneurysmen, Visusverlust) und therapieassoziierten Komplikationen getroffen werden.

Abstract

Treatment of giant cell arteritis (GCA) with high-dose glucocorticoids (GC) regularly leads to a control of the inflammatory activity, so that high-dose GC is still the recommended standard treatment in the current guidelines; however, after discontinuation of GC treatment or reduction of the GC dosage, relapses occur in up to 70% of patients in the further course of the disease, making it necessary to resume treatment or increase the dosage. As a consequence many patients therefore have to be treated with GC often in high doses over several years, which results in a high cumulative exposure to GC. The risk for GC-associated diseases, such as diabetes, glaucoma, osteoporosis or severe infections is therefore significantly increased for patients with giant cell arteritis. For patients with GC-associated comorbidities or increased risk of developing them or patients with a relapse, the current guidelines therefore recommend GC-sparing treatment with tocilizumab or alternatively methotrexate. It is currently unclear over what period of time patients should be treated with GC and GC-sparing treatment, since high-quality study data on de-escalation strategies for GCA are currently still lacking. Decisions on treatment duration and intensity must therefore be made individually for each patient, taking into account general and patient-specific risk factors for a GC-dependent course, GCA-associated vascular damage (stenoses, aneurysms, visual loss) and treatment-associated complications.

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Correspondence to Bernhard Hellmich.

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B. Hellmich war federführend bzw. koordinativ an der Erstellung der EULAR-Recommendations 2018 und der DGRh-Leitlinie zum Management der Großgefäßvaskulitiden beteiligt und hat folgende Zuwendungen von der Industrie erhalten: Vortragshonorare: AbbVie, BMS, Celgene, Novartis, Orgentec, Pfizer, Roche, Sifor. Honorare für Beratungsleistungen: Boehringer, BMS, InflaRx, GSK, Roche.

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C. Fiehn, Baden-Baden

J. Holle, Neumünster

F. Moosig, Neumünster

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Hellmich, B. Glukokortikoide in der Therapie der Riesenzellarteriitis. Z Rheumatol 80, 322–331 (2021). https://doi.org/10.1007/s00393-021-00975-8

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