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Sustained response with ixekizumab treatment of moderate-to-severe psoriasis with scalp involvement: results from three phase 3 trials (UNCOVER-1, UNCOVER-2, UNCOVER-3)
被引:40
|作者:
Reich, Kristian
[1
]
Leonardi, Craig
[2
]
Lebwohl, Mark
[3
]
Kerdel, Francisco
[4
]
Okubo, Yukari
[5
]
Romiti, Ricardo
[6
]
Goldblum, Orin
[7
]
Dennehy, Ellen B.
[7
]
Kerr, Lisa
[7
]
Sofen, Howard
[8
]
机构:
[1] Dermatol Hamburg & SCIderm GmbH, Stephanspl 5, D-20354 Hamburg, Germany
[2] St Louis Univ, Sch Med, Dept Dermatol, St Louis, MO USA
[3] Icahn Sch Med Mt Sinai, Dept Dermatol, New York, NY 10029 USA
[4] Florida Acad Dermatol Ctr, Miami, FL USA
[5] Tokyo Med Univ, Dept Dermatol, Shinjuku Ku, Tokyo, Japan
[6] Univ Sao Paulo, Hosp Clin, Dept Dermatol, Fac Med, Sao Paulo, Brazil
[7] Eli Lilly & Co, Indianapolis, IN 46285 USA
[8] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Dermatol, Los Angeles, CA 90095 USA
关键词:
Psoriasis;
scalp;
clinical trial;
UNCOVER;
ixekizumab;
interleukin-17A;
SEVERE PLAQUE PSORIASIS;
SKIN;
D O I:
10.1080/09546634.2016.1249820
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background: Scalp is a frequently affected and difficult-to-treat area in psoriasis patients.Objective: We assessed the efficacy of ixekizumab in the treatment of patients with scalp psoriasis over 60 weeks using the Psoriasis Scalp Severity Index (PSSI).Methods: In three Phase 3, multicenter, double-blind, placebo-controlled trials, patients with moderate-to-severe psoriasis in UNCOVER-1 (N=1296), UNCOVER-2 (N=1224) and UNCOVER-3 (N=1346) were randomized to subcutaneous 80mg ixekizumab every two weeks (Q2W) or every four weeks (Q4W) after a 160mg starting dose, or placebo through Week 12. Additional UNCOVER-2 and UNCOVER-3 cohorts were randomized to 50mg bi-weekly etanercept through Week 12. Patients entering the open-label long-term extension (LTE) (UNCOVER-3) received ixekizumab Q4W; UNCOVER-1 and UNCOVER-2 included a blinded maintenance period in which static physician global assessment (sPGA) 0/1 responders were re-randomized to placebo, ixekizumab Q4W, or 80mg ixekizumab every 12 weeks (Q12W) through Week 60.Results: In patients with moderate-to-severe psoriasis with baseline scalp involvement, PSSI 90 and 100 were achieved at Week 12 in higher percentages of patients treated with ixekizumab Q2W (81.7% and 74.6%) or ixekizumab Q4W (75.6% and 68.9%) compared with patients treated with placebo (7.6% and 6.7%; p<.001 each ixekizumab arm versus placebo) or etanercept (55.5% and 48.1%; p<.001 each ixekizumab arm versus etanercept). These outcomes were maintained through Week 60 of the maintenance (UNCOVER-1 and UNCOVER-2) and LTE (UNCOVER-3) period in patients who continued on ixekizumab Q4W.Conclusion: Ixekizumab was efficacious in treating scalp psoriasis in patients with moderate-to-severe psoriasis, with most patients achieving complete or near-complete resolution of scalp psoriasis and maintaining this response over 60 weeks.
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页码:282 / 287
页数:6
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