University Medical Center, Geneva, Switzerland.
Br J Dermatol. 2011 Aug;165(2):399-406. doi: 10.1111/j.1365-2133.2011.10399.x. Epub 2011 Jul 11.
CHAMPION was a phase III trial that compared adalimumab with methotrexate and placebo for chronic plaque psoriasis.
To determine the relationship between methotrexate dosing and improvement in psoriasis for patients in CHAMPION.
Methotrexate-treated patients in CHAMPION received step-up dosing to 15 mg per week during the first 8 weeks. At week 8, PASI 50 responders (early responders, ER) were to continue with 15 mg weekly for the next 8 weeks; PASI 50 nonresponders were to receive 20 mg weekly for the next 4 weeks, followed by 20 mg weekly if they achieved ≥ PASI 50 at week 12 (late responders, LR), or 25 mg weekly if not (late nonresponders, LN). Outcomes were assessed post hoc for patients in these groups who completed CHAMPION.
One hundred and three methotrexate-treated patients were analysed: 40 ER, 22 LR and 41 LN. Week 16 mean percentage improvement from baseline in Psoriasis Area and Severity Index was greatest in the ER group, nearly as good in LR, and poor in LN; PASI 75/90/100 response rates were 70%/32%/18%, 41%/9%/5% and 5%/0%/0%, respectively. Among patients with a PASI 75 response at week 16, 72% were in the ER group (comprising 27% of patients overall) and 23% were in the LR group.
Nearly all week 16 PASI 75 responders in CHAMPION achieved a PASI 50 response at week 8 or 12, with maximum methotrexate dosages of 15 or 20 mg per week, respectively. Week 12 may be an appropriate time to discontinue methotrexate treatment in patients who are not achieving good responses.
CHAMPION 是一项针对慢性斑块状银屑病的 III 期临床试验,比较阿达木单抗与甲氨蝶呤和安慰剂的疗效。
确定 CHAMPION 中接受甲氨蝶呤治疗的患者的甲氨蝶呤剂量与银屑病改善之间的关系。
CHAMPION 中接受甲氨蝶呤治疗的患者在前 8 周接受逐步加量至每周 15 毫克。在第 8 周时,PASI 50 应答者(早期应答者,ER)继续每周 15 毫克治疗接下来的 8 周;PASI 50 无应答者在前 4 周接受每周 20 毫克治疗,接下来如果在第 12 周达到≥PASI 50(晚期应答者,LR),则继续每周 20 毫克治疗,如果没有达到(晚期无应答者,LN),则每周 25 毫克治疗。对完成 CHAMPION 的这些组别的患者进行了事后评估。
对 103 名接受甲氨蝶呤治疗的患者进行了分析:40 名 ER、22 名 LR 和 41 名 LN。从基线开始,第 16 周时银屑病面积和严重程度指数的平均改善百分比在 ER 组最大,LR 组接近,LN 组较差;PASI 75/90/100 应答率分别为 70%/32%/18%、41%/9%/5%和 5%/0%/0%。在第 16 周达到 PASI 75 应答的患者中,72%在 ER 组(占所有患者的 27%),23%在 LR 组。
在 CHAMPION 中,几乎所有在第 16 周达到 PASI 75 应答的患者在第 8 周或第 12 周时均达到 PASI 50 应答,分别使用每周 15 或 20 毫克的最大甲氨蝶呤剂量。在第 12 周时,如果患者没有获得良好的应答,可能需要停止甲氨蝶呤治疗。