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Clinical, Patient-Reported, and Ultrasound Outcomes from an Open-Label, 12-week Observational Study of Certolizumab Pegol in Spanish Patients with Rheumatoid Arthritis with or without Prior Anti-TNF Exposure
被引:1
|作者:
Blanco, Francisco J.
[1
]
Rubio-Romero, Esteban
[2
]
Sanmarti, Raimon
[3
]
Diaz-Torne, Cesar
[4
]
Talavera, Pablo
[5
]
Dunkel, Jochen
[6
]
Naredo, Esperanza
[7
,8
]
机构:
[1] INIBIC Complejo Hosp Univ A Coruna, La Coruna, Spain
[2] Hosp Univ Virgen del Rocio, Seville, Spain
[3] Hosp Clin Barcelona, Barcelona, Spain
[4] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[5] UCB Pharma, Madrid, Spain
[6] UCB Pharma, Monheim, Germany
[7] Hosp Fdn Jimenez Diaz, Dept Rheumatol, Madrid, Spain
[8] Hosp Fdn Jimenez Diaz, Joint & Bone Res Unit, Madrid, Spain
来源:
关键词:
Certolizumab pegol;
Rheumatoid Arthritis;
Anti-TNF;
Observational;
Ultrasound;
DOPPLER ULTRASONOGRAPHIC ASSESSMENT;
DISEASE-ACTIVITY;
PREDICTIVE-VALUE;
REMISSION;
THERAPY;
INHIBITORS;
VALIDITY;
CRITERIA;
D O I:
10.1016/j.reuma.2018.07.009
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Objectives: To assess the effectiveness and safety of certolizumab pegol (CZP) in Spanish patients with RA. Materials and methods: SONAR (NCT01526434), a 12-week, open-label, prospective, observational, multicenter study. Patients with active RA for >= 3 months, according to ACR criteria, were treated with CZP (400 mg at Weeks 0, 2 and 4, then 200 mg every 2 weeks). The primary effectiveness endpoint was change from baseline (CFB) in Health Assessment Questionnaire-Disability Index (HAQ-DI) at Week 12. Other assessments included DAS28(ESR), patient's assessment of arthritis pain (PtAAP-VAS) and Short Form 36-item Health Survey (SF-36) physical component summary (PCS) and mental component summary (MCS). Joint inflammation was investigated using Power Doppler (PD) ultrasound (US), to detect effusion, synovial hypertrophy and synovial PD signal. PDUS outcomes assessed CFB to Week 12 in synovial hypertrophy, effusion and PD signal indices. Results: A total of 77/80 enrolled patients received >= 1 dose of CZP. The 12-week mean reduction from baseline (SD) was -0.6 (0.6) for HAQ-DI and -2.2 (1.5) for DAS28(ESR). PtAAP-VAS was reduced from baseline (mean [SD]: -36.8 [26.8]) and improvements in SF-36 PCS and SF-36 MCS were reported. Synovial hypertrophy, effusion and PD signal indices were reduced from baseline to Week 12. One death was reported during the study. Conclusions: Spanish patients with RA demonstrated improvements in clinical, PDUS and patient-reported outcomes over 12 weeks of CZP treatment. No new safety signals were identified, and the safety profile was in line with previous CZP studies. These results support previous clinical trial findings investigating CZP treatment for active RA. (C) 2018 The Authors. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页码:345 / 352
页数:8
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