Baylor University Medical Center, Dallas, TX, USA.
Dermatology Centre, Salford Royal NHS Foundation Trust, Manchester Academic Health, Science Centre, University of Manchester, Manchester, UK.
J Eur Acad Dermatol Venereol. 2017 Oct;31(10):1686-1692. doi: 10.1111/jdv.14237. Epub 2017 Apr 26.
Palmoplantar psoriasis has significant physical and emotional impact on patients and can be difficult to treat.
To evaluate the efficacy of ixekizumab in the treatment of patients with moderate-to-severe plaque psoriasis and moderate-to-severe non-pustular palmoplantar involvement.
In three phase 3, double-blind, placebo-controlled trials, patients with moderate-to-severe non-pustular plaque psoriasis [UNCOVER-1 (N = 1296), UNCOVER-2 (N = 1224), UNCOVER-3 (N = 1346)] were randomized to subcutaneous 80 mg ixekizumab every 2 or 4 weeks (Q2W, Q4W), after a 160-mg starting dose, or placebo through week 12. Additional UNCOVER-2 and UNCOVER-3 cohorts were randomized to 50 mg etanercept biweekly. Patients entering the open-label long-term extension (UNCOVER-3) received ixekizumab Q4W weeks 12-60. Moderate-to-severe palmoplantar involvement was defined as Palmoplantar Psoriasis Area and Severity Index (PPASI) ≥8.
Twenty-eight percent of UNCOVER-1, UNCOVER-2 and UNCOVER-3 patients had baseline palmoplantar involvement (PPASI ≥0, n = 1092) and 9.1% (n = 350) had moderate-to-severe involvement, with mean baseline PPASI ~20, PASI ~24, and most (>60%) had static Physician's Global Assessment ≥4. Higher percentages of patients treated with ixekizumab vs. placebo or etanercept achieved PPASI 50 (approximately 80% vs. 32.9%, 67.8%; ixekizumab, placebo, etanercept, respectively) and PPASI 75 (approximately 70% vs. 18.8%, 44.1%; ixekizumab, placebo, etanercept, respectively) at week 12 (all P < 0.05). PPASI 100 was achieved by higher percentages of ixekizumab-treated patients vs. placebo (approximately 50% vs. 8.2%, P < 0.001) and ixekizumab Q2W-treated patients vs. etanercept (51.8% vs. 32.2%, P < 0.05). Outcomes were maintained or improved in patients continuing on ixekizumab Q4W through week 60. Differences between ixekizumab and placebo or etanercept were statistically significant as early as week 1.
In a subpopulation analysis of patients from phase 3 trials with moderate-to-severe non-pustular palmoplantar involvement and moderate-to-severe plaque psoriasis, ixekizumab treatment resulted in greater and more rapid improvements than placebo and etanercept at week 12; improvements were sustained with continued treatment.
掌跖银屑病会对患者的身体和心理造成显著影响,且治疗难度较大。
评估依奇珠单抗治疗中重度斑块状银屑病和中重度非脓疱性掌跖受累患者的疗效。
在三项 3 期、双盲、安慰剂对照试验中,中重度非脓疱性斑块状银屑病患者(UNCOVER-1[N=1296]、UNCOVER-2[N=1224]、UNCOVER-3[N=1346])按 160mg 起始剂量随机接受皮下注射 80mg 依奇珠单抗每 2 周(Q2W)或每 4 周(Q4W)、安慰剂治疗,至第 12 周。另外 UNCOVER-2 和 UNCOVER-3 队列患者随机接受依那西普每 2 周 50mg 治疗。进入开放标签长期扩展研究(UNCOVER-3)的患者在第 12-60 周接受 Q4W 依奇珠单抗治疗。中重度掌跖受累定义为掌跖银屑病面积和严重程度指数(PPASI)≥8。
28%的 UNCOVER-1、UNCOVER-2 和 UNCOVER-3 患者基线时存在掌跖受累(PPASI≥0,n=1092),9.1%(n=350)存在中重度受累,基线时平均 PPASI 约为 20,PASI 约为 24,大多数(>60%)患者静态医师总体评估≥4。与安慰剂或依那西普相比,接受依奇珠单抗治疗的患者在第 12 周时达到 PPASI 50(约 80%比 32.9%、67.8%;依奇珠单抗、安慰剂、依那西普分别)和 PPASI 75(约 70%比 18.8%、44.1%;依奇珠单抗、安慰剂、依那西普分别)的比例更高(均 P<0.05)。与安慰剂相比(约 50%比 8.2%,P<0.001),接受依奇珠单抗治疗的患者和接受依奇珠单抗 Q2W 治疗的患者与接受依那西普治疗的患者相比(约 51.8%比 32.2%,P<0.05),达到 PPASI 100 的比例更高。接受依奇珠单抗 Q4W 治疗的患者在第 60 周时的结局保持或改善。与安慰剂或依那西普相比,依奇珠单抗的疗效在第 1 周时就具有统计学意义。
在中重度非脓疱性掌跖受累和中重度斑块状银屑病患者的 3 期试验的亚组分析中,与安慰剂和依那西普相比,依奇珠单抗治疗在第 12 周时可更快更显著地改善患者病情;持续治疗可保持疗效。