Department of Internal Medicine, Division of Rheumatology, University of South Florida, Tampa, FL, USA.
Clin Rheumatol. 2012 Nov;31(11):1605-10. doi: 10.1007/s10067-012-2059-4. Epub 2012 Aug 26.
The administration of 100 mg of methylprednisolone intravenously (IV) 1/2 h prior to rituximab decreases the incidence of acute infusion reactions (AIRs). However, this pretreatment adds considerable time and conveys potential risk. We performed an open-label prospective assessment of oral prednisone as a pretreatment to rituximab. This was a 26-week open-label trial of 40 mg of oral prednisone given 1/2 h prior to rituximab as a prophylaxis against AIRs in patients with rheumatoid arthritis (RA). The primary endpoint was AIRs in the first 24 h after their initial infusion. Secondary endpoints include AIRs during the 24 h following their second infusion and any adverse events experienced during the 26-week study; efficacy measures were also followed as secondary endpoints. Sixty-four subjects were screened, and 50 subjects qualified. Fourteen out of the 50 (28 %) subjects had AIRs within 24 h of their first infusion. There were four AIRs (8.3 %) within 24 h of their second infusion. One of day 0 AIRs required drug discontinuation (wheezing/bronchospasm). Forty out of 50 (80 %) subjects experienced an adverse event during the 26 weeks. There were three SAEs deemed not to be study-drug related. The DAS28 and HAQ-DI all improved significantly at weeks 8, 16, and 26 compared to baseline. Historical controls demonstrate that 27 % of RA subjects experience AIRs with their first rituximab infusion. Our data suggest a smaller dose of oral prednisone is an effective alternative to IV methylprednisolone as a pretreatment for rituximab in patients with RA.
静脉注射 100 毫克甲基强的松龙(IV)预处理可降低利妥昔单抗急性输注反应(AIRs)的发生率。然而,这种预处理会增加相当多的时间,并带来潜在的风险。我们对利妥昔单抗前用口服泼尼松作为预处理进行了开放性、前瞻性评估。这是一项为期 26 周的开放性研究,40 毫克口服泼尼松在利妥昔单抗前 1/2 小时给药,作为类风湿关节炎(RA)患者预防 AIRs 的药物。主要终点是首次输注后 24 小时内的 AIRs。次要终点包括第二次输注后 24 小时内的 AIRs 以及在 26 周研究期间经历的任何不良事件;疗效指标也作为次要终点进行随访。共筛选了 64 例患者,其中 50 例符合条件。50 例中有 14 例(28%)在首次输注后 24 小时内发生 AIRs。第二次输注后 24 小时内有 4 例 AIRs(8.3%)。其中 1 例在第 0 天的 AIRs 需要停药(喘息/支气管痉挛)。50 例中有 40 例(80%)在 26 周期间经历了不良事件。有 3 例严重不良事件(SAE)被认为与研究药物无关。与基线相比,DAS28 和 HAQ-DI 在第 8、16 和 26 周均显著改善。历史对照表明,27%的 RA 患者在首次接受利妥昔单抗输注时会发生 AIRs。我们的数据表明,RA 患者利妥昔单抗前用小剂量口服泼尼松是 IV 甲基强的松龙预处理的有效替代方法。