Abatacept Monotherapy Versus Abatacept Plus Methotrexate for Treatment-Refractory Rheumatoid Arthritis.


Journal

American journal of therapeutics
ISSN: 1536-3686
Titre abrégé: Am J Ther
Pays: United States
ID NLM: 9441347

Informations de publication

Date de publication:
Historique:
pubmed: 13 10 2017
medline: 16 11 2019
entrez: 13 10 2017
Statut: ppublish

Résumé

Methotrexate combination therapy improves abatacept efficacy as a first-line biologic agent for the treatment of rheumatoid arthritis, but it is unclear when abatacept is used later on, particularly after non-TNF inhibitor (TNFi) failure. The objective of this study was to determine whether treatment response after non-TNFi inadequate response is different in patients with rheumatoid arthritis (RA) treated with abatacept in combination with or not with methotrexate. Patients treated with abatacept monotherapy or in combination with methotrexate after non-TNFi failure were included. Data from 46 patients aged 56 years [49-61] with 12 years [8-16] of disease duration were examined. Rituximab was the treatment used in the previous line for 75.0% of the combination therapy group (15/20) and 34.6% (9/26) in the monotherapy group. At 12 months, 38.5% (10/26) of patients were in good-to-moderate EULAR response in the monotherapy group compared with 25.0% (5/20) in the combination therapy group (P = 0.33). Treatment persistence at 12 months was 61.5% (16/26) in the monotherapy group and 35.0% (7/20) in the combination therapy group (P = 0.07). Adding methotrexate to abatacept did not improve treatment response in patients with RA after non-TNFi inadequate response.

Sections du résumé

BACKGROUND BACKGROUND
Methotrexate combination therapy improves abatacept efficacy as a first-line biologic agent for the treatment of rheumatoid arthritis, but it is unclear when abatacept is used later on, particularly after non-TNF inhibitor (TNFi) failure.
STUDY QUESTION OBJECTIVE
The objective of this study was to determine whether treatment response after non-TNFi inadequate response is different in patients with rheumatoid arthritis (RA) treated with abatacept in combination with or not with methotrexate.
METHODS METHODS
Patients treated with abatacept monotherapy or in combination with methotrexate after non-TNFi failure were included.
RESULTS RESULTS
Data from 46 patients aged 56 years [49-61] with 12 years [8-16] of disease duration were examined. Rituximab was the treatment used in the previous line for 75.0% of the combination therapy group (15/20) and 34.6% (9/26) in the monotherapy group. At 12 months, 38.5% (10/26) of patients were in good-to-moderate EULAR response in the monotherapy group compared with 25.0% (5/20) in the combination therapy group (P = 0.33). Treatment persistence at 12 months was 61.5% (16/26) in the monotherapy group and 35.0% (7/20) in the combination therapy group (P = 0.07).
CONCLUSIONS CONCLUSIONS
Adding methotrexate to abatacept did not improve treatment response in patients with RA after non-TNFi inadequate response.

Identifiants

pubmed: 29023282
doi: 10.1097/MJT.0000000000000645
doi:

Substances chimiques

Antirheumatic Agents 0
Abatacept 7D0YB67S97
Methotrexate YL5FZ2Y5U1

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e358-e363

Auteurs

Tristan Pascart (T)

Department of Rheumatology, Saint-Philibert Hospital, Lille University, Lomme, France.
Department of Rheumatology, University-Hospital of Lille, Lille Cedex, France.
EA 4490, University-Hospital of Lille, Lille Cedex, France.

Peggy Philippe (P)

Department of Rheumatology, University-Hospital of Lille, Lille Cedex, France.

Elodie Drumez (E)

Department of Biostatistics, EA2694, University of Lille, CHRU Lille, Lille, France.

Xavier Deprez (X)

Department of Rheumatology, Valenciennes Hospital, Valenciennes, France.

Bernard Cortet (B)

Department of Rheumatology, University-Hospital of Lille, Lille Cedex, France.
EA 4490, University-Hospital of Lille, Lille Cedex, France.

Alain Duhamel (A)

Department of Biostatistics, EA2694, University of Lille, CHRU Lille, Lille, France.

Eric Houvenagel (E)

Department of Rheumatology, Saint-Philibert Hospital, Lille University, Lomme, France.

René-Marc Flipo (RM)

Department of Rheumatology, University-Hospital of Lille, Lille Cedex, France.

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Classifications MeSH