Efficacy and management of tocilizumab in polymyalgia rheumatica: results of a multicentre retrospective observational study

Author:

Assaraf Morgane1,Chevet Baptiste23ORCID,Wendling Daniel4ORCID,Philippe Peggy1ORCID,Cailliau Emeline5ORCID,Roux Christian6ORCID,Avouac Jérôme7ORCID,Delacour Mathilde8,Houvenagel Eric9ORCID,Sellam Jérémie10ORCID,Cortet Bernard1ORCID,Henry Julien11,Flipo René-Marc1ORCID,Devauchelle-Pensec Valérie23

Affiliation:

1. Rheumatology Department, ULR 4490, Université de Lille, Lille University Hospital , Lille, France

2. Rheumatology Department and Centre de Référence de Maladies Auto-Immunes Rares de l’Adulte (CERAINO), CHU de Brest , Brest, France

3. LBAI UMR 1227, Université de Brest, Inserm, CHU de Brest , Brest, France

4. Rheumatology Department, CHU Besançon, EA 4266 Université de Franche-Comté , Besançon, France

5. Biostatistics Department, CHU Lille , Lille, France

6. Rheumatology Department, CNRS, INSERM, iBV, Université Cote d’Azur, CHU Nice , Nice, France

7. Rheumatology Department, Hôpital Cochin, AP-HP, Centre—Université Paris Cité , Paris, France

8. Rheumatology Department, CH Arras , Arras, France

9. Rheumatology Department, CH Lhomme , Lhomme, France

10. Rheumatology Department, Hôpital Saint-Antoine, AP-HP, INSERM UMRS_938, Sorbonne Université , Paris, France

11. Rheumatology Department, AP-HP, Université Paris Saclay, Hôpital Bicêtre , Le Kremlin-Bicêtre, France

Abstract

Abstract Objectives The efficacy of anti-IL-6 receptors such as tocilizumab (TCZ) was demonstrated in patients with PMR in two recent randomized controlled trials. The objective of this multicentre retrospective study was to assess the efficacy of TCZ in PMR patients requiring glucocorticoid (GC)-sparing treatment, as well as different strategies for TCZ withdrawal. Methods We conducted a multicentre study in French tertiary healthcare departments for patients with PMR. PMR patients receiving off-label TCZ between 2015 and 2022 were included. The primary endpoint was the proportion of patients tapering to GCs ≤5 mg/day 6 months after the first TCZ infusion. The secondary endpoints were the proportion in whom GC was discontinued during follow-up, and the proportion of patients in whom TCZ was discontinued. Results Fifty-three PMR patients were included. Thirty-one patients suffered from active PMR despite conventional synthetic DMARDs. GCs were ≤5 mg/day in 77% of the patients (95% CI 36–89) at 6 months, and in 97% of the patients at 12 months. Six and 12 months after the first TCZ infusion, the proportions of GC-free patients were 22.5% (95% CI 12.7–37.8) and 58.3% (95% CI 43.2–74.1), respectively. Among TCZ withdrawal strategies, TCZ infusion spacing and TCZ dose reduction were more successful (success in 87% and 79% of attempts, respectively) than TCZ discontinuation (success in 52% of attempts; P = 0.012 and P = 0.039, respectively). Conclusion In GC-dependent PMR patients, treatment with TCZ led to a drastic decrease in GC dose and remission of PMR. TCZ dose reduction or TCZ infusion spacing are good options to consider in TCZ withdrawal.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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