University College London Division of Medicine and Royal Free Hospital, London, UK.
Department of Rheumatology, Cliniques Universitaires Saint-Luc & Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Brussels, Belgium.
Clin Exp Rheumatol. 2021 Sep-Oct;39 Suppl 132(5):51-58. doi: 10.55563/clinexprheumatol/e92f7o. Epub 2021 Oct 6.
To evaluate the effect of canakinumab on health-related quality of life (HRQoL), work/school and social life of patients with autoinflammatory recurrent fever syndromes, including colchicine-resistant familial Mediterranean fever, mevalonate kinase deficiency, and tumour necrosis factor receptor-associated periodic syndrome, in the CLUSTER trial.
HRQoL of patients who received canakinumab 150 mg or 300 mg every four weeks in the CLUSTER trial (n=173) was assessed at baseline and Weeks 17 and 41. For children we used the Child Health Questionnaire - Parent Form 50 (CHQ-PF50), including psychosocial (PsS) and physical (PhS) component summary scores. For adults, the Short-Form-12 (SF-12) Health Survey was used, including physical (PFS) and mental (PCS) component summary scores. The Sheehan Disability Scale (SDS) was used to determine the impact of treatment on work/school, social and family life.
The results obtained were remarkably consistent in both paediatric and adult patients across the three disease cohorts. At baseline, median scores for physical components were relatively low (26-29 for PhS and 34-38 for PFS); they improved to values similar to those expected in the general population by Week 17, and this improvement was sustained at Week 41, when median PhS scores were 47-50 and PFS 44-54. Psychosocial and mental scores also improved from baseline to Week 17 and 41, with scores comparable to the general population. Notable improvements were also observed in the SDS scale.
Patients with three inherited autoinflammatory syndromes experienced sustained improvements on their HRQoL, work/school, and social life on treatment with canakinumab.
评估卡那奴单抗对自身炎症性复发性发热综合征(包括对秋水仙碱耐药的家族性地中海热、甲羟戊酸激酶缺乏症和肿瘤坏死因子受体相关周期性综合征)患者健康相关生活质量(HRQoL)、工作/学校和社会生活的影响,该研究为 CLUSTER 试验。
在 CLUSTER 试验中,接受卡那奴单抗 150mg 或 300mg 每四周一次治疗的患者在基线和第 17 周和第 41 周评估 HRQoL。对于儿童,我们使用儿童健康问卷 - 家长形式 50 项(CHQ-PF50),包括心理社会(PsS)和身体(PhS)成分综合评分。对于成年人,使用简短形式-12(SF-12)健康调查,包括身体(PFS)和心理(PCS)成分综合评分。使用希恩残疾量表(SDS)来确定治疗对工作/学校、社会和家庭生活的影响。
在三个疾病队列的儿科和成年患者中,获得的结果非常一致。基线时,身体成分的中位数评分相对较低(PhS 为 26-29,PFS 为 34-38);到第 17 周,评分改善至类似于一般人群的预期值,到第 41 周,评分持续改善,PhS 中位数评分为 47-50,PFS 为 44-54。心理社会和心理评分也从基线改善到第 17 周和第 41 周,评分与一般人群相当。在 SDS 量表上也观察到显著的改善。
接受卡那奴单抗治疗的三种遗传性自身炎症性综合征患者的 HRQoL、工作/学校和社会生活得到持续改善。