Certolizumab Pegol for the Treatment of Plaque Psoriasis in Routine Clinical Practice: One-Year Results from the CIMREAL Study.

IF 3.5 3区 医学 Q1 DERMATOLOGY
Dermatology and Therapy Pub Date : 2024-08-01 Epub Date: 2024-06-27 DOI:10.1007/s13555-024-01210-3
Bernhard Korge, Olivier Vanhooteghem, Charles W Lynde, Alena Machovcova, Marc Perrussel, Elisavet Lazaridou, Claudio Marasca, David Vidal Sarro, Ines Duenas Pousa, Frederik Fierens, Paulette Williams, Saori Shimizu, Tanja Heidbrede, Richard B Warren
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引用次数: 0

Abstract

Introduction: Certolizumab pegol (CZP) is an anti-tumor necrosis factor alpha (TNFα) approved for the treatment of moderate to severe plaque psoriasis (PSO). However, data on its real-world use is currently limited. The objective of this study was to describe the 1-year real-world effectiveness of CZP, its impact on health-related quality of life (HRQoL), and safety outcomes in patients with moderate to severe PSO in multi-country settings.

Methods: CIMREAL, a prospective, noninterventional study, was conducted across Europe and Canada from August 2019 to December 2022. Patients were followed for 1-year, receiving CZP 400 mg initial doses at weeks 0, 2, and 4, followed by CZP 200 mg every 2 weeks (Q2W) or CZP 400 mg Q2W maintenance dosing. Effectiveness was assessed using the Psoriasis Area and Severity Index (PASI) and Dermatology Life Quality Index (DLQI). Safety was also evaluated.

Results: Overall, 399 patients with moderate to severe PSO were included. Of these, 93.7% (374/399) and 77.9% (311/399) completed months 3 and 12, respectively. Mean age (± standard deviation) was 42.9 ± 13.5 years and body mass index was 28.5 ± 6.8 kg/m2, with the majority of patients being female (68.2%). At 12 months, CZP showed substantial effectiveness, achieving PASI 75 and PASI 90 response rates (≥ 75% and ≥ 90% improvement from baseline, respectively) of 77% and 56.5%, respectively. Patients with PASI score of ≤ 3 and ≤ 2 experienced improvement from 3 months (49.8% and 41.1%, respectively) to 12 months (82.0% and 75.3%, respectively). HRQoL considerably improved, with mean DLQI scores decreasing from 12.4 to 2.3 after 12 months of treatment, and the proportion of patients with DLQI 0/1 increased from 28.6% at 3 months to 59.4% at 12 months. The 1-year probability of persistence was approximately 85%. Overall, 30.6% of the patients experienced any adverse events and 9.3% had serious adverse events.

Conclusion: In routine clinical practice, CZP exhibited consistent effectiveness, positively impacting both skin psoriasis activity and HRQoL. The 1-year persistence of CZP was high, and no new safety signals were identified.

Trial registration number: ClinicalTrials.gov Identifier: NCT04053881 https://www.

Clinicaltrials: gov/study/NCT04053881 .

Abstract Image

常规临床实践中用于治疗斑块状银屑病的 Certolizumab Pegol:CIMREAL研究的一年结果。
简介赛妥珠单抗 pegol(CZP)是一种抗肿瘤坏死因子α(TNFα)药物,已被批准用于治疗中度至重度斑块状银屑病(PSO)。然而,目前有关其实际使用情况的数据还很有限。本研究旨在描述CZP的1年实际疗效、其对健康相关生活质量(HRQoL)的影响以及在多国环境中对中重度斑块型银屑病患者的安全性结果:CIMREAL是一项前瞻性、非介入性研究,于2019年8月至2022年12月在欧洲和加拿大开展。患者接受为期1年的随访,在第0、2和4周接受CZP 400毫克初始剂量,随后每2周服用CZP 200毫克(Q2W)或CZP 400毫克(Q2W)维持剂量。疗效采用银屑病面积和严重程度指数(PASI)和皮肤病生活质量指数(DLQI)进行评估。此外,还对安全性进行了评估:共纳入了 399 名中度至重度 PSO 患者。其中,93.7%(374/399)和 77.9%(311/399)的患者分别完成了第 3 个月和第 12 个月的治疗。平均年龄(± 标准差)为 42.9 ± 13.5 岁,体重指数为 28.5 ± 6.8 kg/m2,大多数患者为女性(68.2%)。12个月后,CZP显示出显著疗效,PASI 75和PASI 90应答率(与基线相比分别改善≥75%和≥90%)分别达到77%和56.5%。PASI评分≤3和≤2的患者在3个月(分别为49.8%和41.1%)至12个月(分别为82.0%和75.3%)期间病情均有改善。患者的 HRQoL 显著改善,治疗 12 个月后,DLQI 平均得分从 12.4 分降至 2.3 分,DLQI 为 0/1 分的患者比例从 3 个月时的 28.6% 增加到 12 个月时的 59.4%。持续 1 年的概率约为 85%。总体而言,30.6%的患者出现任何不良事件,9.3%的患者出现严重不良事件:在常规临床实践中,CZP表现出一致的有效性,对皮肤银屑病的活动性和HRQoL都有积极影响。CZP的1年持续率很高,没有发现新的安全信号:试验注册号:ClinicalTrials.gov Identifier:NCT04053881 https://www.Clinicaltrials: gov/study/NCT04053881 。
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来源期刊
Dermatology and Therapy
Dermatology and Therapy Medicine-Dermatology
CiteScore
6.00
自引率
8.80%
发文量
187
审稿时长
6 weeks
期刊介绍: Dermatology and Therapy is an international, open access, peer-reviewed, rapid publication journal (peer review in 2 weeks, published 3–4 weeks from acceptance). The journal is dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of dermatological therapies. Studies relating to diagnosis, pharmacoeconomics, public health and epidemiology, quality of life, and patient care, management, and education are also encouraged. Areas of focus include, but are not limited to all clinical aspects of dermatology, such as skin pharmacology; skin development and aging; prevention, diagnosis, and management of skin disorders and melanomas; research into dermal structures and pathology; and all areas of aesthetic dermatology, including skin maintenance, dermatological surgery, and lasers. The journal is of interest to a broad audience of pharmaceutical and healthcare professionals and publishes original research, reviews, case reports/case series, trial protocols, and short communications. Dermatology and Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an International and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of quality research, which may be considered of insufficient interest by other journals. The journal appeals to a global audience and receives submissions from all over the world.
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