Werth Victoria P, Furie Richard A, Romero-Diaz Juanita, Navarra Sandra, Kalunian Kenneth, van Vollenhoven Ronald F, Nyberg Filippa, Kaffenberger Benjamin H, Sheikh Saira Z, Radunovic Goran, Huang Xiaobi, Clark George, Carroll Hua, Naik Himanshu, Gaudreault Francois, Meyers Adam, Barbey Catherine, Musselli Cristina, Franchimont Nathalie
From the University of Pennsylvania and Corporal Michael J. Crescenz Veterans Affairs Medical Center - both in Philadelphia (V.P.W.); Northwell Health, Great Neck, NY (R.A.F.); Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubrián, Mexico City (J.R.-D.); the University of Santo Tomas, Manila, Philippines (S.N.); the University of California, San Diego, La Jolla (K.K.); Amsterdam University Medical Centers, Amsterdam (R.F.V.); Karolinska University Hospital, Stockholm (F.N.); Ohio State University, Columbus (B.H.K.); University of North Carolina at Chapel Hill, Chapel Hill (S.Z.S.); Institute of Rheumatology, University of Belgrade, Belgrade, Serbia (G.R.); Biogen, Cambridge, MA (X.H., G.C., H.C., H.N., F.G., A.M., C.M., N.F.); and Biogen, Baar, Switzerland (C.B.).
N Engl J Med. 2022 Jul 28;387(4):321-331. doi: 10.1056/NEJMoa2118024.
Blood dendritic cell antigen 2 (BDCA2) is a receptor that is exclusively expressed on plasmacytoid dendritic cells, which are implicated in the pathogenesis of lupus erythematosus. Whether treatment with litifilimab, a humanized monoclonal antibody against BDCA2, would be efficacious in reducing disease activity in patients with cutaneous lupus erythematosus has not been extensively studied.
In this phase 2 trial, we randomly assigned adults with histologically confirmed cutaneous lupus erythematosus with or without systemic manifestations in a 1:1:1:1 ratio to receive subcutaneous litifilimab (at a dose of 50, 150, or 450 mg) or placebo at weeks 0, 2, 4, 8, and 12. We used a dose-response model to assess whether there was a response across the four groups on the basis of the primary end point, which was the percent change from baseline to 16 weeks in the Cutaneous Lupus Erythematosus Disease Area and Severity Index-Activity score (CLASI-A; scores range from 0 to 70, with higher scores indicating more widespread or severe skin involvement). Safety was also assessed.
A total of 132 participants were enrolled; 26 were assigned to the 50-mg litifilimab group, 25 to the 150-mg litifilimab group, 48 to the 450-mg litifilimab group, and 33 to the placebo group. Mean CLASI-A scores for the groups at baseline were 15.2, 18.4, 16.5, and 16.5, respectively. The difference from placebo in the change from baseline in CLASI-A score at week 16 was -24.3 percentage points (95% confidence interval [CI] -43.7 to -4.9) in the 50-mg litifilimab group, -33.4 percentage points (95% CI, -52.7 to -14.1) in the 150-mg group, and -28.0 percentage points (95% CI, -44.6 to -11.4) in the 450-mg group. The least squares mean changes were used in the primary analysis of a best-fitting dose-response model across the three drug-dose levels and placebo, which showed a significant effect. Most of the secondary end points did not support the results of the primary analysis. Litifilimab was associated with three cases each of hypersensitivity and oral herpes infection and one case of herpes zoster infection. One case of herpes zoster meningitis occurred 4 months after the participant received the last dose of litifilimab.
In a phase 2 trial involving participants with cutaneous lupus erythematosus, treatment with litifilimab was superior to placebo with regard to a measure of skin disease activity over a period of 16 weeks. Larger and longer trials are needed to determine the effect and safety of litifilimab for the treatment of cutaneous lupus erythematosus. (Funded by Biogen; LILAC ClinicalTrials.gov number, NCT02847598.).
血液树突状细胞抗原2(BDCA2)是一种仅在浆细胞样树突状细胞上表达的受体,浆细胞样树突状细胞与红斑狼疮的发病机制有关。针对BDCA2的人源化单克隆抗体利蒂菲单抗治疗皮肤型红斑狼疮患者是否能有效降低疾病活动度尚未得到广泛研究。
在这项2期试验中,我们将组织学确诊的有或无全身表现的皮肤型红斑狼疮成年患者按1:1:1:1的比例随机分组,在第0、2、4、8和12周接受皮下注射利蒂菲单抗(剂量分别为50、150或450 mg)或安慰剂。我们使用剂量反应模型,根据主要终点评估四组患者是否有反应,主要终点是皮肤型红斑狼疮疾病面积和严重程度指数-活动评分(CLASI-A;评分范围为0至70,分数越高表明皮肤受累越广泛或严重)从基线到16周的变化百分比。同时也评估了安全性。
共招募了132名参与者;26名被分配到50 mg利蒂菲单抗组,25名被分配到150 mg利蒂菲单抗组,48名被分配到450 mg利蒂菲单抗组,33名被分配到安慰剂组。各组基线时的平均CLASI-A评分分别为15.2、18.4、16.5和16.5。在第16周时,50 mg利蒂菲单抗组CLASI-A评分相对于基线的变化与安慰剂组相比为-24.3个百分点(95%置信区间[CI] -43.7至-4.9),150 mg组为-33.4个百分点(95% CI,-52.7至-14.1),450 mg组为-28.0个百分点(95% CI,-44.6至-11.4)。在对三个药物剂量水平和安慰剂进行的最佳拟合剂量反应模型的主要分析中使用了最小二乘均值变化,结果显示有显著效果。大多数次要终点不支持主要分析结果。利蒂菲单抗与3例超敏反应和口腔疱疹感染以及1例带状疱疹感染相关。1例带状疱疹脑膜炎发生在参与者接受最后一剂利蒂菲单抗4个月后。
在一项涉及皮肤型红斑狼疮参与者的2期试验中,在16周的时间里,利蒂菲单抗治疗在衡量皮肤疾病活动度方面优于安慰剂。需要进行更大规模、更长时间的试验来确定利蒂菲单抗治疗皮肤型红斑狼疮的效果和安全性。(由百健公司资助;LILAC ClinicalTrials.gov编号,NCT02847598。)