Single-Center Cross-Sectional Analysis of Patients with RA, SpA, and PsA: Data from the Prescription Database.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Maurizio Benucci, Francesca Li Gobbi, Emanuele Antonio Maria Cassarà, Anna Lucia Marigliano, Alessandro Mannoni, Enrico Benvenuti
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引用次数: 0

Abstract

Introduction. The Italian Committee for Tailored BIOlogic Therapy (ITABIO), in a first report, has reviewed the literature to identify the best strategy for the choice of second-line biologic therapy in patients with rheumatoid arthritis (RA), spondyloarthritis (SpA), and psoriatic arthritis (PsA). To verify the application of ITABIO recommendations in real life and how the recommendations perform in maintaining the health status of patients affected by inflammatory arthritis (RA, SpA, PsA), a database has been developed by Pharmaceutical Governance to evaluate the appropriateness of prescriptions. Methods. We have analyzed retrospectively 616 patients, 288 (46.7%) affected by RA, 117 (19%) affected by SpA, and 211 (34.3%) affected by PsA. Age, sex, diagnosis, current treatment, previous treatments with csDMARDs, b-DMARDs, ts-DMARDs, presence of risk factors for cardiovascular (CV) events, liver disease, infections, extra-articular manifestations such as interstitial lung disease (ILD) for RA, enthesitis, dactylitis, uveitis, inflammatory bowel disease for SpA and PsA, neoplasms, diabetes, presence or absence of rheumatoid factor (RF) and anti-citrullinated peptide antibodies (ACPA) for RA were evaluated. Results. The percentage of treatments with anti-TNF biosimilars was 65.1, 52.4, and 24.3% in SpA (76 patients(pt)), PsA (110 pt), and RA (69 pt), respectively. The percentage of monotherapy was 68% (418 pt) in the three diseases. For RA, 34.2% of patients were difficult to treat (D2T) (98 pt), 54.8% (157 pt) were in monotherapy (tocilizumab-sarilumab-upadacitinib-filgotinib). Abatacept was the most prescribed treatment in RF and ACPA-positive patients and in those with ILD. The anti-IL-17A secukinumab was prescribed in 12% of SpA, of which 71% had enthesitis and dactylitis (14 pt). Ixekizumab was prescribed in 10.4% of PsA patients over 65 years with previous CV events, enthesitis, and dactylitis (21 pt). Apremilast was present in 71% of PsA with previous cancer. Conclusions. The cross-sectional analysis of prescriptions in patients with RA, SpA, and PsA demonstrates how the ITABIO recommendations can guide towards the correct appropriateness of prescription. RA and especially D2T-RA remains the disease with the greatest therapeutic failures, with the highest percentage of monotherapy (anti-IL-6 and Jak-i) and of discontinuation of MTX.

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RA、SpA和PsA患者的单中心横断面分析:来自处方数据库的数据。
介绍。意大利定制生物治疗委员会(ITABIO)在第一份报告中回顾了文献,以确定类风湿关节炎(RA)、脊椎关节炎(SpA)和银屑病关节炎(PsA)患者选择二线生物治疗的最佳策略。为了验证ITABIO建议在现实生活中的应用,以及这些建议在维持炎症性关节炎(RA, SpA, PsA)患者健康状况方面的表现,Pharmaceutical Governance开发了一个数据库来评估处方的适当性。方法。我们回顾性分析了616例患者,其中RA患者288例(46.7%),SpA患者117例(19%),PsA患者211例(34.3%)。评估年龄、性别、诊断、目前治疗情况、既往csDMARDs、b-DMARDs、ts-DMARDs治疗、心血管(CV)事件、肝脏疾病、感染、关节外表现(如RA的间质性肺疾病(ILD)、鼻炎、趾炎、葡萄膜炎、SpA和PsA的炎症性肠病、肿瘤、糖尿病、RA的类风湿因子(RF)和抗葡氨酸肽抗体(ACPA)的存在或不存在)等危险因素。结果。在SpA(76例)、PsA(110例)和RA(69例)中,抗tnf生物类似药的治疗比例分别为65.1、52.4和24.3%。在这三种疾病中,单药治疗的百分比为68%(418例)。对于RA, 34.2%的患者难以治疗(D2T)(98例),54.8%(157例)采用单药治疗(tocilizumab-sarilumab-upadacitinib-filgotinib)。阿巴接受是RF和acpa阳性患者以及ILD患者最常用的治疗方法。12%的SpA患者使用抗il - 17a secukinumab,其中71%的SpA患者患有鼻炎和指炎(14例)。10.4%的65岁以上伴有CV事件、鼻炎和趾炎的PsA患者使用Ixekizumab(21例)。71%的PsA既往癌症患者存在阿普拉米司特。结论。对RA、SpA和PsA患者处方的横断面分析表明ITABIO建议如何指导处方的正确适当性。RA,尤其是D2T-RA仍然是治疗失败最多的疾病,单药治疗(抗il -6和jak - 1)和MTX停药的比例最高。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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