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Relapse after cessation of weekly tocilizumab for giant cell arteritis: a multicentre service evaluation in England

  • the TOC STOP 2022 Investigators
  • Bedfordshire Hospitals NHS Foundation Trust
  • Royal Devon University Healthcare NHS Foundation Trust
  • Newcastle upon Tyne Hospitals NHS Foundation Trust
  • Lancaster University
  • University Hospitals of Morecambe Bay NHS Foundation Trust
  • Sheffield Teaching Hospitals NHS Foundation Trust
  • Mid and South Essex NHS Foundation Trust
  • University Hospital Southampton NHS Foundation Trust
  • University Hospitals of Leicester NHS Trust
  • Oxford University Hospitals NHS Foundation Trust
  • University of Oxford
  • Norfolk and Norwich University Hospitals NHS Foundation Trust
  • University Hospital Coventry
  • University of Warwick
  • King's College Hospital NHS Foundation Trust
  • Cambridge University Hospitals NHS Foundation Trust
  • Royal Cornwall Hospitals NHS Trust
  • University Hospitals Dorset NHS Foundation Trust
  • University of Leeds
  • University College London Hospitals NHS Foundation Trust
  • Stockport NHS Foundation Trust
  • University of Bath
  • Royal United Hospitals Bath NHS Foundation Trust
  • University of Liverpool
  • The National Behcet’s Centre of Excellence
  • Manchester Royal Infirmary
  • University of the West of England
  • University Hospitals Bristol and Weston NHS Foundation Trust
  • NIHR Leeds Biomedical Research Centre

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)
2 Downloads (Pure)

Abstract

Objectives: The National Health Service in England funds 12 months of weekly s.c. tocilizumab (qwTCZ) for patients with relapsing or refractory GCA. During the coronavirus disease 2019 (COVID-19) pandemic, some patients were allowed longer treatment. We sought to describe what happened to patients after cessation of qwTCZ. Methods: Multicentre service evaluation of relapse after stopping qwTCZ for GCA. The log-rank test was used to identify significant differences in time to relapse. Results: A total of 336 GCA patients were analysed from 40 centres, treated with qwTCZ for a median [interquartile range (IQR)] of 12 (12–17) months. At time of stopping qwTCZ, median (IQR) prednisolone dose was 2 (0–5) mg/day. By 6, 12 and 24 months after stopping qwTCZ, 21.4%, 35.4% and 48.6%, respectively, had relapsed, requiring an increase in prednisolone dose to a median (IQR) of 20 (10–40) mg/day. 33.6% relapsers had a major relapse as defined by EULAR. Time to relapse was shorter in those that had previously also relapsed during qwTCZ treatment (P ¼ 0.0017), in those not in remission at qwTCZ cessation (P ¼ 0.0036) and in those with large vessel involvement on imaging (P ¼ 0.0296). Age ≥65 years, gender, GCA-related sight loss, qwTCZ treatment duration, TCZ taper, prednisolone dosing and conventional synthetic DMARD use were not associated with time to relapse. Conclusion: Up to half our patients with GCA relapsed after stopping qwTCZ, often requiring a substantial increase in prednisolone dose. One-third of relapsers had a major relapse. Extended use of TCZ or repeat treatment for relapse should be considered for these patients.

Original languageEnglish
Pages (from-to)3407-3414
Number of pages8
JournalRheumatology
Volume63
Issue number12
DOIs
Publication statusPublished - 11 Nov 2023
Externally publishedYes

Keywords

  • giant cell arteritis
  • NICE guidance
  • relapse
  • service evaluation
  • tocilizumab
  • vasculitis
  • Recurrence
  • Prednisolone/administration & dosage
  • Drug Administration Schedule
  • Humans
  • Middle Aged
  • Giant Cell Arteritis/drug therapy
  • England/epidemiology
  • Male
  • SARS-CoV-2
  • COVID-19/epidemiology
  • Antibodies, Monoclonal, Humanized/administration & dosage
  • Aged, 80 and over
  • Female
  • Aged
  • Glucocorticoids/administration & dosage

ASJC Scopus subject areas

  • Rheumatology
  • Pharmacology (medical)

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