Real-World Evidence for Baricitinib in the Treatment of Rheumatoid Arthritis in Spain: A Systematic Literature Review

被引:1
作者
Rosas, Jose [1 ]
Belzunegui, Joaquin [2 ]
Hernandez-Cruz, Blanca [3 ]
Aguirregabiria, Itxaso [4 ]
Moyano, Sebastian [4 ]
Cobo, Amelia [4 ]
Diaz-Cerezo, Silvia [4 ]
机构
[1] Marina Baixa Hosp, Rheumatol Dept, Ave Alcalde Jaume Botella Mayor 7, Alicante 03570, Spain
[2] Donostia Univ Hosp, Rheumatol Dept, Guipuzcoa 20014, Spain
[3] Univ Hosp Virgen Macarena, Rheumatol Dept, Calle Dr Fedriani 3, Seville 41009, Spain
[4] Eli Lilly & Co, Avda Ind 30 Alcobendas, Madrid 28108, Spain
关键词
Baricitinib; Rheumatoid arthritis; Systematic; Spain; Real-world; INADEQUATE RESPONSE; EFFICACY; SAFETY; TOFACITINIB; DISEASE;
D O I
10.1007/s12325-025-03161-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
IntroductionBaricitinib is a Janus kinase inhibitor approved for the treatment of moderate-to-severe rheumatoid arthritis (RA) in adults who have responded inadequately, or are intolerant, to disease-modifying antirheumatic drugs (DMARDs). This systematic literature review was conducted to understand the use of baricitinib in RA in the real-world setting in Spain.MethodsEmbase and MEDLINE databases were systematically searched for publications (in English or Spanish) published between March 2017 and June 2023; Spanish data presented at national rheumatology congresses were also obtained, with a date limitation of 2021-2023.ResultsNineteen eligible publications were identified (5 full papers, 14 conference abstracts), including more than 1000 patients who received baricitinib for RA in Spain. Most patients were older and female with long disease duration, and moderate-to-severe active disease. Studies included both biologic DMARD-experienced and DMARD-na & iuml;ve patients, and most patients received baricitinib 4 mg/day. Baricitinib persistence ranged from 6 to 48 months, with ineffectiveness (primary or secondary) being the most frequently reported reason for discontinuation. Baricitinib was consistently shown to decrease disease activity, across all outcome measures (Disease Activity Score-28 for RA, the Simplified and Clinical Disease Activity Indexes, swollen and tender joint counts and patient-reported outcomes). Thirteen studies reported safety outcomes, with discontinuation rates due to adverse events ranging from 9.5 to 20%. Across these studies, adverse events of interest included eleven cases of herpes zoster, six serious infections, two major adverse cardiovascular events, and three malignant neoplasms.ConclusionThese results suggest baricitinib is effective in the real-world setting in Spain, with a consistent safety profile, similar to findings reported in clinical studies and in real-world studies conducted in other countries.
引用
收藏
页码:2403 / 2428
页数:26
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