Withdrawal of infliximab therapy in ankylosing spondylitis in persistent clinical remission, results from the REMINEA study.


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
05 04 2019
Historique:
received: 27 11 2018
accepted: 22 03 2019
entrez: 7 4 2019
pubmed: 7 4 2019
medline: 9 4 2020
Statut: epublish

Résumé

Recent data suggest that anti-TNF doses can be reduced in ankylosing spondylitis (AS) patients. Some authors even propose withdrawing treatment in patients in clinical remission; however, at present there is no evidence to support this. To assess how long AS patients with persistent clinical remission remained free of flares after anti-TNF withdrawal and to evaluate the effects of treatment reintroduction. We also analyze the characteristics of patients who did not present clinical relapse. Multicenter, prospective, observational study of a cohort of patients with active AS who had received infliximab as a first anti-TNF treatment and who presented persistent remission (more than 6 months). We recorded at baseline and every 6-8 weeks over the 12-month period the age, gender, disease duration, peripheral arthritis or enthesitis, HLA-B27 status, BASDAI, CRP, ESR, BASFI, and three visual analogue scales, spine global pain, spinal night time pain, and patient's global assessment. Thirty-six out of 107 patients (34%) presented persistent remission and were included in our study. After treatment withdrawal, 21 of these 36 patients (58%) presented clinical relapse during follow-up. Infliximab therapy was reintroduced and only 52% achieved clinical remission, as they had before the discontinuation of infliximab; in an additional 10%, reintroduction of infliximab was ineffective, obliging us to change the anti-TNF therapy. No clinical or biological factors were associated with the occurrence of relapse during the follow-up. Two thirds of patients in clinical remission presented clinical relapse shortly after infliximab withdrawal. Although the reintroduction of infliximab treatment was safe, half of the patients did not present the same clinical response that they had achieved prior to treatment withdrawal.

Sections du résumé

BACKGROUND
Recent data suggest that anti-TNF doses can be reduced in ankylosing spondylitis (AS) patients. Some authors even propose withdrawing treatment in patients in clinical remission; however, at present there is no evidence to support this.
OBJECTIVE
To assess how long AS patients with persistent clinical remission remained free of flares after anti-TNF withdrawal and to evaluate the effects of treatment reintroduction. We also analyze the characteristics of patients who did not present clinical relapse.
METHODS
Multicenter, prospective, observational study of a cohort of patients with active AS who had received infliximab as a first anti-TNF treatment and who presented persistent remission (more than 6 months). We recorded at baseline and every 6-8 weeks over the 12-month period the age, gender, disease duration, peripheral arthritis or enthesitis, HLA-B27 status, BASDAI, CRP, ESR, BASFI, and three visual analogue scales, spine global pain, spinal night time pain, and patient's global assessment.
RESULTS
Thirty-six out of 107 patients (34%) presented persistent remission and were included in our study. After treatment withdrawal, 21 of these 36 patients (58%) presented clinical relapse during follow-up. Infliximab therapy was reintroduced and only 52% achieved clinical remission, as they had before the discontinuation of infliximab; in an additional 10%, reintroduction of infliximab was ineffective, obliging us to change the anti-TNF therapy. No clinical or biological factors were associated with the occurrence of relapse during the follow-up.
CONCLUSIONS
Two thirds of patients in clinical remission presented clinical relapse shortly after infliximab withdrawal. Although the reintroduction of infliximab treatment was safe, half of the patients did not present the same clinical response that they had achieved prior to treatment withdrawal.

Identifiants

pubmed: 30953541
doi: 10.1186/s13075-019-1873-3
pii: 10.1186/s13075-019-1873-3
pmc: PMC6451276
doi:

Substances chimiques

Antirheumatic Agents 0
HLA-B27 Antigen 0
Tumor Necrosis Factor-alpha 0
Infliximab B72HH48FLU

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

88

Investigateurs

Arturo Rodriguez-de-la-Serna (A)
Victoria Hernandez (V)
Elena Riera (E)
Vera Ortiz (V)
Teresa Clavaguera (T)
Patricia Reyner (P)
Miquel Sala (M)
Agustí Sellas (A)
Concepció Pitarch (C)
Delia Reina (D)
Jordi Blanco (J)
Montse Centelles (M)
Ramon Figuls (R)
Mario Gelman (M)
Xavier Arasa (X)
Maria Bonet (M)
Manel Ciria (M)

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Auteurs

Mireia Moreno (M)

Rheumatology Department, Parc Taulí Hospital Universitari, I3PT, Universitat Autònoma de Barcelona, 08208, Sabadell, Barcelona, Spain.

Jordi Gratacós (J)

Rheumatology Department, Parc Taulí Hospital Universitari, I3PT, Universitat Autònoma de Barcelona, 08208, Sabadell, Barcelona, Spain. jgratacosmas@gmail.com.

Vicenç Torrente-Segarra (V)

Rheumatology Department, Hospital Comarcal de l'Alt Penedès, Vilafranca, Barcelona, Spain.

Raimon Sanmarti (R)

Rheumatology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.

Rosa Morlà (R)

Rheumatology Department, Hospital del Vendrell, Tarragona, Spain.

Caridad Pontes (C)

Clinical Pharmacology Department, ParcTaulí Hospital Universitari, I3PT, Universitat Autònoma de Barcelona, Sabadell, Barcelona, Spain.

Maria Llop (M)

Rheumatology Department, Parc Taulí Hospital Universitari, I3PT, Universitat Autònoma de Barcelona, 08208, Sabadell, Barcelona, Spain.

Xavier Juanola (X)

Rheumatology Department, Hospital Universitari de Bellvitge, IDIBELL, Universitat de Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.

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Classifications MeSH