IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Arthritis Rheumatol. 2015 Mar;67(3):840-8. doi: 10.1002/art.38984.
To investigate the impact of tocilizumab treatment on growth and growth-related laboratory parameters in patients with systemic juvenile idiopathic arthritis (JIA) enrolled in a phase III clinical trial.
Patients with systemic JIA ages 2-17 years (n = 112) received tocilizumab in a 12-week, randomized, placebo-controlled period and a long-term open-label extension. Height velocity and standard deviation (SD) score; levels of insulin-like growth factor 1 (IGF-1), osteocalcin (OC), and C-telopeptide of type I collagen (CTX-I); and Juvenile Arthritis Disease Activity Score in 71 joints (JADAS-71) were measured in a post hoc analysis of 83 patients who never received growth hormone and did not reach Tanner stage 5 by the end of the first year of treatment.
Patients had stunted growth at baseline (mean height SD score -2.2). During tocilizumab treatment, males (73%) and females (83%) experienced above-normal mean height velocities of 6.6 cm/year (P < 0.0001 versus World Health Organization norms). Mean height SD score increases during year 1 (0.29) and year 2 (0.31) were significant (both P < 0.0001). The mean SD score for IGF-1 levels increased significantly (-0.2 for year 1 and -0.1 for year 2 versus -1.0 at baseline; both P < 0.0001). Mean OC and CTX-I levels (both P < 0.0001) and the OC:CTX-I ratio (P = 0.014) significantly increased from baseline to year 2. In multiple regression analysis, first-year height velocity had a significant inverse relationship to JADAS-71 at year 1, age, mean glucocorticoid dosage during the year, and height SD score at baseline.
Our findings indicate that during treatment with tocilizumab, patients with systemic JIA experience significant catch-up growth, normalization of IGF-1 levels, and bone balance improvement favoring bone formation.
研究托珠单抗治疗对纳入 III 期临床试验的全身型幼年特发性关节炎(JIA)患者生长及相关实验室参数的影响。
112 例 2-17 岁全身型 JIA 患者接受为期 12 周的随机、安慰剂对照期及长期开放性扩展研究,采用托珠单抗治疗。对从未接受过生长激素治疗且在治疗第 1 年末未达到 Tanner 第 5 期的 83 例患者进行了事后分析,测量了身高速度和标准差(SD)评分;胰岛素样生长因子 1(IGF-1)、骨钙素(OC)和 I 型胶原 C 端肽(CTX-I)水平;71 关节少年关节炎疾病活动评分(JADAS-71)。
患者基线时存在生长迟缓(平均身高 SD 评分-2.2)。托珠单抗治疗期间,73%的男性和 83%的女性身高速度超过正常,平均为 6.6cm/年(P<0.0001 与世界卫生组织标准相比)。第 1 年(0.29)和第 2 年(0.31)平均身高 SD 评分增加有显著意义(均 P<0.0001)。IGF-1 水平的平均 SD 评分显著增加(第 1 年和第 2 年分别为-0.2 和-0.1,与基线时的-1.0 相比,均 P<0.0001)。OC 和 CTX-I 水平的平均值(均 P<0.0001)和 OC:CTX-I 比值(P=0.014)从基线至第 2 年均显著升高。在多元回归分析中,第 1 年的身高速度与第 1 年的 JADAS-71、年龄、当年平均糖皮质激素剂量和基线时的身高 SD 评分呈显著负相关。
我们的发现表明,在托珠单抗治疗期间,全身型 JIA 患者经历了显著的追赶性生长,IGF-1 水平正常化,骨平衡改善,有利于骨形成。