TABLE 9Infliximab efficacy outcomes: uncontrolled follow-up data

TrialDuration (weeks)OutcomesInfliximab/placebo
IMPACT7981,89,96,109,111,113115,117,11850ACR 20All pts34/49 (69.4%)
+MTX16/22 (72.7%)
−MTX18/27 (66.7%)
ACR 5026/49 (53.1%)
ACR 7019/49 (38.8%)
PsARC36/49 (73.5%)
HAQ: mean (SD)% change from baseline(n = 45) −42.5 (59.0)
PASI 50a19/22 (86.3%)
PASI 75a13/22 (59%)
PASI 90a9/22 (40.9%)
PASI: mean (SD) change from baselinea(n = 35) −4.8 (5.9)
Total modified van der Heijde–Sharp score: mean (SD) change from baseline(n = 70) −1.72 (5.82)
IMPACT 282,90,91,95,98,106,112,11654PsARC67/90 (74.4%)
PASI 50a57/82 (69.5%)
PASI 75a40/82 (48.8%)
PASI 90a32/82 (39%)
Total modified van der Heijde–Sharp score: mean (SD) change from baselineInfliximab/infliximab −0.94 (3.4)

Placebo/infliximab 0.53 (2.6)

pts, patients.

a

PASI 50/75/90 outcomes are for subgroup of patients with ≥ 3% BSA psoriasis.

From: 3, Assessment of clinical effectiveness

Cover of Etanercept, Infliximab and Adalimumab for the Treatment of Psoriatic Arthritis: A Systematic Review and Economic Evaluation
Etanercept, Infliximab and Adalimumab for the Treatment of Psoriatic Arthritis: A Systematic Review and Economic Evaluation.
Health Technology Assessment, No. 15.10.
Rodgers M, Epstein D, Bojke L, et al.
Southampton (UK): NIHR Journals Library; 2011 Feb.
© 2011, Crown Copyright.

Included under terms of UK Non-commercial Government License.

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.