Gulliver Wayne P, Randell Shane, Gulliver Susanne, Gregory Valerie, Nagle Sean, Chambenoit Olivier
1 Newlab Clinical Research, St John's, NL, Canada.
2 Department of Medicine, Faculty of Medicine, Memorial University of Newfoundland, St John's, NL, Canada.
J Cutan Med Surg. 2018 Nov/Dec;22(6):567-576. doi: 10.1177/1203475418786712. Epub 2018 Jun 28.
Plaque psoriasis affects approximately 2% to 3% of the global population, with psoriatic arthritis observed in approximately 20% to 30% of these individuals. Upon advances in research pathophysiology and treatment over the past decade, biologic therapies have been used more to treat moderate to severe psoriasis. In Canada, reimbursement bodies have defined prior authorization criteria to determine patient eligibility for funding of biologic treatments in moderate to severe plaque psoriasis. Generally, patients will have been treated with conventional therapies such as topical steroids, phototherapy, or systemic treatments such as methotrexate and cyclosporine before starting a biologic therapy. In difficult cases or severe flares in otherwise controlled disease, practitioners may augment the regimen with one or more conventional treatments. The objective of this observational report was to identify treatment pathways for psoriasis and psoriatic arthritis patients in Canada by examining initial biologic treatment and subsequent treatment optimization patterns for informed reimbursement discussions and decisions. A retrospective chart review was conducted at Newlab Clinical Research using medical records of patients who received at least 1 of 4 biologic agents approved at that time of the survey in Canada for the treatment of plaque psoriasis (adalimumab, etanercept, infliximab, ustekinumab). The study population consisted of patients who had moderate to severe plaque psoriasis, diagnosed by a dermatologist, for at least 6 months before the study index date and who attended Newlab Clinical Research between 2008 and 2013. All current and previous agents prescribed for the treatment of psoriasis were captured. A total of 248 patients with psoriasis treated with biologics were identified, of whom 27 (10.9%) were also diagnosed with psoriatic arthritis. Prior to initiating treatment with a biologic, most patients (72.1%) were treated with (or contraindicated to) methotrexate/cyclosporine. Treatment was supplemented with topical agents (70.6%) and/or followed by a course of ultraviolet light phototherapy (51.6%). Only 2.4% of patients were treated with a biologic first. Of 248 patients treated with biologics, almost half (47.6%) needed add-on therapy, whereas 16.5% of patients had an increase in dose or dosing interval. Furthermore, 14.1% of patients added a topical agent, 10.5% a topical steroid, or 6.5% a course of phototherapy while continuing biologic therapies. Finally, 30.4% of patients switched to another biologic treatment. Adalimumab was the most common agent used as a second-line agent (37.2%), and patients who started on adalimumab mainly switched to ustekinumab as a second-line agent (73.9%). Infliximab was the agent least often used as second-line therapy.
斑块状银屑病影响着全球约2%至3%的人口,其中约20%至30%的患者会出现银屑病关节炎。在过去十年研究病理生理学和治疗取得进展后,生物疗法更多地用于治疗中度至重度银屑病。在加拿大,报销机构已制定了预先授权标准,以确定患者是否有资格获得中度至重度斑块状银屑病生物治疗的资金。一般来说,患者在开始生物治疗前会接受传统疗法,如局部用类固醇、光疗,或全身治疗,如甲氨蝶呤和环孢素。在病情难以控制或在原本病情得到控制的情况下出现严重病情发作时,医生可能会用一种或多种传统治疗方法来加强治疗方案。本观察性报告的目的是通过检查初始生物治疗及后续治疗优化模式,为加拿大银屑病和银屑病关节炎患者确定治疗途径,以进行知情的报销讨论和决策。在Newlab临床研究中心进行了一项回顾性病历审查,使用了在调查时加拿大已批准用于治疗斑块状银屑病的4种生物制剂(阿达木单抗、依那西普、英夫利昔单抗、乌司奴单抗)中至少使用过1种的患者的病历。研究人群包括在研究索引日期前至少6个月被皮肤科医生诊断为中度至重度斑块状银屑病且在2008年至2013年期间在Newlab临床研究中心就诊的患者。记录了所有当前和以前开具的用于治疗银屑病的药物。共确定了248例接受生物制剂治疗的银屑病患者,其中27例(10.9%)也被诊断为银屑病关节炎。在开始生物治疗前,大多数患者(72.1%)接受过甲氨蝶呤/环孢素治疗(或对其有禁忌)。治疗辅以局部用药(70.6%)和/或随后进行一个疗程的紫外线光疗(51.6%)。只有2.4%的患者首先接受生物制剂治疗。在248例接受生物制剂治疗的患者中,几乎一半(47.6%)需要追加治疗,而16.5%的患者增加了剂量或给药间隔。此外,14.1%的患者在继续生物治疗的同时添加了局部用药,10.5%添加了局部用类固醇,或6.5%进行了一个疗程的光疗。最后,30.4%的患者改用另一种生物治疗。阿达木单抗是最常用的二线药物(37.2%),开始使用阿达木单抗的患者主要改用乌司奴单抗作为二线药物(73.9%)。英夫利昔单抗是最不常被用作二线治疗的药物。