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A prospective randomized controlled trial comparing infliximab and etanercept in patients with moderate-to-severe chronic plaque-type psoriasis: the Psoriasis Infliximab vs. Etanercept Comparison Evaluation (PIECE) study
被引:32
|作者:
de Vries, A. C. Q.
[1
]
Thio, H. B.
[3
]
de Kort, W. J. A.
[5
]
Opmeer, B. C.
[2
]
van der Stok, H. M.
[1
]
de Jong, E. M. G. J.
[6
]
Horvath, B.
[7
]
Busschbach, J. J. V.
[4
]
Nijsten, T. E. C.
[3
]
Spuls, Ph. I.
[1
]
机构:
[1] Acad Med Ctr, Dept Dermatol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Acad Med Ctr, Clin Res Unit, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[3] Erasmus MC, Dept Dermatol, NL-3015 CA Rotterdam, Netherlands
[4] Erasmus MC, Med Psychol & Psychotherapy Sect, NL-3015 CA Rotterdam, Netherlands
[5] Amphia Hosp, Dept Dermatol, Molengracht 21, NL-4818 CK Breda, Netherlands
[6] Radboud Univ Nijmegen Med Ctr, Dept Dermatol, Rene Descartesdreef 1, NL-6525 GL Nijmegen, Netherlands
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Dermatol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands
关键词:
SF-36 HEALTH SURVEY;
QUALITY-OF-LIFE;
DOUBLE-BLIND;
MAINTENANCE THERAPY;
PHASE-III;
EFFICACY;
IMPROVEMENT;
SAFETY;
INDUCTION;
PLACEBO;
D O I:
10.1111/bjd.14867
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background There are currently no independent data available comparing infliximab and etanercept for the treatment of psoriasis. Objectives To compare these biologics without funding from pharmaceutical companies. Methods Overall, 50 patients were randomized to etanercept (n = 23) 50 mg subcutaneously twice weekly or infliximab (n = 25) 5 mg kg(-1) intravenously at week 0, 2, 6, 14 and 22. After 24 weeks, 19 patients stopped and 22 continued treatment and were followed up to week 48. The primary outcome was >= 75% improvement of Psoriasis Area and Severity Index (PASI 75) at week 24. The secondary outcomes included PASI 75 at week 6 (onset of action) and week 12, Investigator's Global Assessment (IGA), Patient Global Assessment, impact on quality of life (Skindex-17 and SF-36), Treatment Satisfaction Questionnaire of Medication, duration of remission, maintenance treatment and safety. Results At week 24, PASI 75 was achieved in 72% (infliximab) vs. 35% (etanercept) (P = 0.01). The onset of action was achieved in 52% (infliximab) and 4% (etanercept). At week 12, 76% (infliximab) and 22% (etanercept) achieved PASI 75 (P < 0.001). At week 24, IGA 'clear or almost clear' was observed in 76% (infliximab) and 30% (etanercept) (P = 0.01). Skindex-17 symptom score was significantly better for infliximab. Maintenance treatment achieved PASI 75 for 67% (n = 6) infliximab vs. 50% (n = 5) etanercept, at week 48 (P = 0.65). Mild adverse events were reported in 76% (infliximab) vs. 66% (etanercept). Conclusions Infliximab showed a rapid and significant higher level of efficacy until week 24 compared with etanercept. Long-term data showed no significant differences between both groups at week 48. Safety parameters were comparable.
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页码:624 / 633
页数:10
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