PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV
PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV
PROGRAMM JAHRESTAGUNG 2012 30. Nov. – 2. Dez ... - ÖGDV
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Poster Psoriasis<br />
P 35<br />
Long-term improvement in patient-reported outcomes after transition from<br />
methotrexate to ustekinumab in moderate to severe psoriasis: TRANSIT Week<br />
52 results<br />
K. Reich 1<br />
L. Puig 2<br />
T. Luger 3<br />
J. Lambert 4<br />
S. Chimenti 5<br />
G. Girolomoni 6<br />
J.-F. Nicolas 7<br />
K. Kragballe 8<br />
S Mistry 9<br />
P Bergmans 10<br />
G. Thompson 9<br />
J. Barker 11<br />
C. Paul 12<br />
1 Georg-August University, Hamburg, Germany<br />
2 Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona,<br />
Spain<br />
3 University of Munster, Munster, Germany<br />
4 Ghent University Hospital, Ghent, Belgium<br />
5 University of Rome, Rome, Italy<br />
6 University of Verona, Verona, Italy<br />
7 University of Lyon, Lyon, France<br />
8 Arhus University, Arhus, Denmark<br />
9 Janssen-Cilag Ltd, High Wycombe, UK<br />
10 Janssen-Cilag BV, Tilburg, Netherlands<br />
11 St John's Institute of Dermatology, King's College, London, UK<br />
12 Larrey Hospital, Paul Sabatier University, Toulouse, France<br />
Introduction & Objectives: The Phase IV TRANSIT study compared outcomes in<br />
psoriasis patients with inadequate response to methotrexate (MTX), following<br />
immediate or gradual transition to ustekinumab. We describe Week 52 quality of life<br />
outcomes. Materials & Methods In this 52-week open-label, parallel group trial, 490<br />
patients with moderate to severe plaque psoriasis despite treatment with MTX<br />
(10-25mg/week for greater than or equal to 8 weeks) were randomised 1:1 to<br />
ustekinumab with either a) immediate cessation of MTX (Arm 1), or b) 4 weeks' overlap<br />
with decreasing MTX dose (Arm 2). Ustekinumab was administered according to label:<br />
45mg in patients less than or equal to 100kg or 90mg if >100kg. Patients less than or<br />
equal to 100kg not achieving adequate response (Psoriasis Area Severity Index decrease<br />
from baseline greater than or equal to 75% [PASI 75]) at Week 28 or Week 40 were dose<br />
87