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Retention Rates of Adalimumab, Etanercept and Infliximab as First and Second-Line Biotherapy in Patients With Rheumatoid Arthritis in Daily Practice

Retention Rates of Adalimumab, Etanercept and Infliximab as First and Second-Line Biotherapy in Patients With Rheumatoid Arthritis in Daily Practice

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01692899
Acronym
MAINTAIN
Enrollment
780
Registered
2012-09-25
Start date
2011-06-30
Completion date
2011-09-30
Last updated
2012-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Keywords

Retention Rates, of Adalimumab, Etanercept and Infliximab, as First and Second-Line Biotherapy, in Patients with Rheumatoid Arthritis, in Daily Practice., TNF inhibitors, biotherapy, retrospective study

Brief summary

To compare retention rates of adalimumab, etanercept and infliximab as first-line biotherapy in rheumatoid arthritis (RA), to determine causes of discontinuation, retention-associated factors, and retention rates of possible second-line tumor necrosis factor α inhibitors (TNFi).

Detailed description

In this retrolective, multicentric study, medical charts of RA patients starting TNFi between March 2005 and April 2009 were reviewed, with follow-up between 2 and 6 years. The retention rate was estimated using the Kaplan-Meier method. Comparison between TNFi was done after adjustment using a Cox model. Factors associated with better retention were identified by multivariate analysis. Medical charts of all patients with RA starting a first TNFα inhibitor therapy between March 1, 2005 (start of commercialization of adalimumab in France) and April 30, 2009 (allowing at least 2 years of follow-up) were systematically reviewed in detail by 2 rheumatologist investigators

Interventions

None listed

Sponsors

scientific steering committee of KOL in rheumatology
CollaboratorUNKNOWN
Pfizer
Lead SponsorINDUSTRY

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* RA defined by the 1987 ACR criteria \[18\] * first TNFα inhibitor prescribed in the previously mentioned period * TNFα inhibitor prescribed as first-line biotherapy * undergone at least one evaluation in the center after treatment initiation

Exclusion criteria

* previously received another biotherapy * TNFα inhibitor was prescribed in an RCT * refused to participate

Design outcomes

Primary

MeasureTime frame
Compare retention rates of adalimumab, etanercept and infliximab administered as first-line biologic therapy in RA2 years

Secondary

MeasureTime frame
Compare retention rates of TNFα inhibitor monoclonal antibodies (adalimumab and infliximab) and the soluble receptor (etanercept)4 years
Causes of discontinuing these treatments4 years
Determine the factors associated with better retention of the first TNFα inhibitors4 years
Compare retention rates of possible second-line TNFα inhibitors4 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026