Global Clinical Pharmacology, Janssen Research & Development, LLC, Spring House, PA, USA.
Immunology Clinical Development, Janssen Research & Development, LLC, Spring House, PA, USA.
J Clin Pharmacol. 2019 Apr;59(4):590-604. doi: 10.1002/jcph.1353. Epub 2018 Dec 11.
Population pharmacokinetics (PK) and exposure-response (E-R) analyses were conducted to compare the PK and E-R relationships of golimumab between children and adults with ulcerative colitis. PK data following subcutaneous golimumab administration to children with ulcerative colitis (6-17 years) in the PURSUIT-PEDS-PK study, adults with ulcerative colitis in the PURSUIT study, and children with pediatric polyarticular juvenile idiopathic arthritis (2-17 years) in the GO-KIDS study, were included in the population PK analysis. E-R analysis was conducted using logistic regression to link serum golimumab concentration and Mayo score-based efficacy outcomes in pediatric and adult ulcerative colitis. Golimumab PK was adequately described by a 1-compartment model with first-order absorption and elimination. Golimumab apparent clearance and volume of distribution increased with body weight. Golimumab apparent clearance was higher in patients with lower serum albumin, no methotrexate use, and positive antibodies to golimumab; age was not an influential factor after accounting for body weight. Model-estimated terminal half-life (9.2 days in children; 9.5 days in adults) and other PK parameters suggest that golimumab PK properties are generally comparable between children and adults with ulcerative colitis. Simulations suggest that a higher induction dose than that tested in PURSUIT-PEDS-PK may be needed for children ≤45 kg to achieve exposures comparable to adults. Comparable E-R relationships between children and adults with ulcerative colitis were observed, although children appeared to be more responsive for the more stringent remission end point. The overall comparable PK and E-R relationships between children and adults support the extrapolation of golimumab efficacy from the adult to the pediatric ulcerative colitis population.
进行群体药代动力学(PK)和暴露-反应(E-R)分析,以比较溃疡性结肠炎儿童和成人中皮下给予戈利木单抗的 PK 和 E-R 关系。群体 PK 分析纳入了 PURSUIT-PEDS-PK 研究中溃疡性结肠炎儿童(6-17 岁)、PURSUIT 研究中溃疡性结肠炎成人以及 GO-KIDS 研究中儿童幼年特发性关节炎多关节型(2-17 岁)的皮下给予戈利木单抗后的 PK 数据。E-R 分析采用逻辑回归将血清戈利木单抗浓度与儿科和成人溃疡性结肠炎的 Mayo 评分疗效结果相关联。戈利木单抗 PK 采用 1 室模型加一级吸收和消除进行充分描述。戈利木单抗表观清除率和分布容积随体重增加而增加。在血清白蛋白较低、未使用甲氨蝶呤和对戈利木单抗有阳性抗体的患者中,戈利木单抗表观清除率较高;在考虑体重后,年龄不是一个影响因素。模型估算的终末半衰期(儿童为 9.2 天;成人 9.5 天)和其他 PK 参数表明,溃疡性结肠炎儿童和成人的戈利木单抗 PK 特性总体上相似。模拟表明,对于≤45kg 的儿童,可能需要比 PURSUIT-PEDS-PK 中测试的更高诱导剂量,以达到与成人相当的暴露量。观察到儿童和成人溃疡性结肠炎之间存在可比的 E-R 关系,尽管对于更严格的缓解终点,儿童似乎更敏感。儿童和成人之间总体相似的 PK 和 E-R 关系支持将戈利木单抗疗效从成人扩展到儿科溃疡性结肠炎人群。