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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

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