Across rheumatic diseases

Effectiveness of non-medical switch from adalimumab bio-originator to SB5 biosimilar and from ABP501 adalimumab biosimilar to SB5 biosimilar in patients with chronic inflammatory arthropathies: a monocentric observational study

Clin Exp RheumatolPublished Observational study

Authors' conclusion

Our results provide a reassuring profile of effectiveness when switching from ADA originator to one of its biosimilars and between two different biosimilars.

Study context

Population
Adults with rheumatoid arthritis (RA), psoriatic arthritis (PsA) or axial spondyloarthritis (axSpA) treated with ADA bio-originator or ABP501 ADA biosimilar who switched to SB5; followed up for 4 months
Participants
110 vs 40
Exposure
Switch from ADA bio-originator to SB5 biosimilar and from ABP501 ADA biosimilar to SB5 biosimilar, before vs after switch
  • ADA bio-originator to SB5n = 110
  • ABP501 to SB5n = 40
Outcome
Remission/low disease activity, ADA bio-originator to SB5
Follow-up
4 months (T4)
Methodological detailsmonocentric, non-medical switch
  • Monocentric
  • Non-medical switch

Main finding

As reported in the abstract

RR for moderate-high disease activity

2.6

95% CI 1.2–5.7

P = 0.01

By group

Observational data: associations, not effects.

Further findings

DAS28-CRP, DAPSA, ASDAS-CRP and BASDAI, ADA bio-originator to SB5 · 4 months

No differences found

Patient global assessment-VAS, ADA bio-originator to SB5 (RA and PsA subgroups) · 4 months

Worsening in RA
P = 0.04
Worsening in PsA
P = 0.02

HAQ, ADA bio-originator to SB5 (PsA subgroup) · 4 months

Worsening in PsA
P = 0.03

DAS28-CRP, DAPSA, remission/low disease activity and patient-reported outcomes (PROs), ABP501 to SB5 · 4 months

No differences compared to baseline

Original publication

Effectiveness of non-medical switch from adalimumab bio-originator to SB5 biosimilar and from ABP501 adalimumab biosimilar to SB5 biosimilar in patients with chronic inflammatory arthropathies: a monocentric observational study. Clin Exp Rheumatol. Published 21 January 2022. doi:10.55563/clinexprheumatol/bf00j9

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.