Papp Kim, Gottlieb Alice B, Naldi Luigi, Pariser David, Ho Vincent, Goyal Kavitha, Fakharzadeh Steven, Chevrier Marc, Calabro Stephen, Langholff Wayne, Krueger Gerald
J Drugs Dermatol. 2015 Jul;14(7):706-14.
Safety surveillance is needed for biologic therapies for psoriasis.
To assess the risk of adverse events of special interest (AEoSIs) with ustekinumab and other psoriasis treatments in a real-world setting using 2014 Psoriasis Longitudinal Assessment and Registry (PSOLAR) data. AEoSIs included malignancy (excluding nonmelanoma skin cancer), major adverse cardiovascular events (MACE), serious infection, and all-cause mortality.
Cumulative rates of AEoSIs/100 patient-years (PY) are reported for ustekinumab, infliximab, other biologics (mostly adalimumab/etanercept), and non-biologics based on pre-specified analyses using attribution rules biased against ustekinumab. Risk factors for AEoSIs, including treatments, were determined using multivariate statistical analysis.
A total of 12,093 patients (40,388 PY) were enrolled in PSOLAR. Overall incidence rates were 0.68/100PY for malignancy, 0.33/100PY for MACE, 1.60/100PY for serious infection, and 0.46/100PY for mortality. Unadjusted rates of serious infection for infliximab (2.91/100PY) and other biologics (1.91/100PY) were numerically higher compared with ustekinumab (0.93/100PY). Exposure to the combined group of biologics other than ustekinumab was significantly associated with serious infection (hazard ratio=1.96, P<.001). None of the biologics was associated with increased risk of malignancy, MACE, or mortality.
Observational data have inherent biases.
Analysis of 2014 PSOLAR data identified no increased risk of malignancy, MACE, serious infection, or mortality with ustekinumab.
银屑病生物疗法需要进行安全性监测。
利用2014年银屑病纵向评估与登记(PSOLAR)数据,在真实世界环境中评估优特克单抗及其他银屑病治疗方法发生特殊关注不良事件(AEoSIs)的风险。AEoSIs包括恶性肿瘤(非黑色素瘤皮肤癌除外)、主要不良心血管事件(MACE)、严重感染和全因死亡率。
根据针对优特克单抗有偏倚的归因规则进行预先指定分析,报告优特克单抗、英夫利昔单抗、其他生物制剂(主要是阿达木单抗/依那西普)和非生物制剂的AEoSIs/100患者年(PY)累积发生率。使用多变量统计分析确定包括治疗方法在内的AEoSIs风险因素。
共有12,093名患者(40,388 PY)纳入PSOLAR。总体发病率为恶性肿瘤0.68/100 PY、MACE 0.33/100 PY、严重感染1.60/100 PY、死亡率0.46/100 PY。英夫利昔单抗(2.91/100 PY)和其他生物制剂(1.91/100 PY)的未调整严重感染发生率在数值上高于优特克单抗(0.93/100 PY)。除优特克单抗外的生物制剂联合使用与严重感染显著相关(风险比=1.96,P<0.001)。没有一种生物制剂与恶性肿瘤、MACE或死亡率风险增加相关。
观察性数据存在固有偏倚。
对2014年PSOLAR数据的分析表明,优特克单抗不会增加恶性肿瘤、MACE、严重感染或死亡率的风险。