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Social media voices on the treatment of skin psoriasis with biologics. 社交媒体上关于生物制剂治疗皮肤牛皮癣的声音。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2126276
Melissa A Nickles, Roger N Haber

Social media is an outlet for patients to share medical experiences with a large audience. However, the impact of such content on individual patient treatment decisions has yet to be fully explored. We characterized patient experiences posted on social media surrounding biologic use for skin psoriasis. We analyzed content from YouTube, Instagram, and TikTok and identified patient experiences with a variety of biologics, most commonly Humira (20.7%), Cosentyx (14.0%), and Stelara (14.0%). The biologic was described as burdensome in about half of all videos/posts (46.4%), and the most commonly cited reasons included adverse effects or abnormal blood tests (12.8%), cost or insurance issues (11.7%), lack or loss of efficacy (11.7%), and pain with injection or injection site reaction (11.7%). Nevertheless, the majority (60.9%) of videos/posts reported an overall positive experience with a biologic for their skin psoriasis, which may inspire reluctant patients to try a biologic recommended by their physician.

社交媒体是患者与广大受众分享医疗经验的渠道。然而,这些内容对个别患者治疗决策的影响尚未得到充分探讨。我们描述了在社交媒体上发布的有关皮肤牛皮癣生物治疗的患者体验。我们分析了来自YouTube、Instagram和TikTok的内容,并确定了患者使用各种生物制剂的经历,最常见的是Humira(20.7%)、Cosentyx(14.0%)和Stelara(14.0%)。大约一半的视频/帖子(46.4%)将生物制剂描述为负担,最常见的原因包括不良反应或血液检查异常(12.8%),成本或保险问题(11.7%),缺乏或丧失疗效(11.7%),以及注射或注射部位反应疼痛(11.7%)。然而,大多数(60.9%)的视频/帖子报告了皮肤牛皮癣生物制剂的总体积极体验,这可能会激励不情愿的患者尝试医生推荐的生物制剂。
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引用次数: 1
Severe papulopustular rosacea successfully treated with a combination of oral azithromycin and isotretinoin. 口服阿奇霉素联合异维甲酸成功治疗严重丘疹性酒渣鼻。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2129953
Hans Christian Ring, Claus Zachariae, Simon Francis Thomsen, Jacob P Thyssen, Alexander Egeberg

Papulopustular rosacea is notoriously a challenge to treat, and treatment options are scarce. Only limited data exist on the use of azithromycin in treatment of papulopustular rosacea. However, the unique pharmacokinetics of azithromycin may have several indications in the treatment of papulopustular rosacea. We here report a case of hard-to-treat papulopustular rosacea which was successfully treated with pulsed oral azithromycin in addition to maintenance isotretinoin.

丘疹性酒渣鼻是一个众所周知的挑战,治疗方案是稀缺的。只有有限的数据存在使用阿奇霉素治疗丘疹性酒渣鼻。然而,阿奇霉素独特的药代动力学在治疗丘疹性酒渣鼻时可能有几个适应症。我们在此报告一个难治性丘疹性酒渣鼻的病例,成功地治疗了脉冲口服阿奇霉素和维持异维甲酸。
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引用次数: 0
Methotrexate dosing regimen for plaque-type psoriasis: an update of a systematic review. 甲氨蝶呤给药方案治疗斑块型银屑病:一项系统综述的更新。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2117539
Astrid M van Huizen, Rosie Sikkel, Anouk G M Caron, Stef P Menting, Phyllis I Spuls

Background: Methotrexate (MTX) is a systemic treatment for plaque-type psoriasis. At the time of approval, no dose-ranging studies were performed. Nowadays, a uniform dosing regimen is lacking. This might contribute to suboptimal treatment with the drug.

Objective: To summarize the literature involving the MTX dosing regimens in psoriasis patients.

Methods: In this SR, RCTs and documents with aggregated evidence (AgEv) on the MTX dosing regimen in psoriasis were summarized. All randomized controlled trials (RCTs) in which oral, subcutaneous or intramuscular MTX was used in patients with psoriasis and AgEv, were included. The MEDLINE, EMBASE and CENTRAL databases were searched up to June 20, 2022. This SR was registered in PROSPERO.

Results: Thirty-nine RCTs had a high risk of bias. Test dosages were given in only 3 RCTs. In the RCTs, MTX was usually prescribed in a start dose of 7.5 mg/week (n = 13). MTX was mostly given in a start dose of 15 mg/week, in the AgEv (n = 5). One guideline recommended a test dose, in other aggregated evidence a test dose was not mentioned or even discouraged.

Conclusions: There is a lack of high-quality evidence and available data for dosing MTX in psoriasis is heterogeneous.

背景:甲氨蝶呤(MTX)是一种治疗斑块型银屑病的全身药物。在批准时,没有进行剂量范围研究。目前,缺乏统一的给药方案。这可能导致该药治疗效果欠佳。目的:总结有关银屑病患者甲氨蝶呤给药方案的文献。方法:对银屑病甲氨蝶呤给药方案的随机对照试验和综合证据(AgEv)文献进行综述。纳入了银屑病和AgEv患者口服、皮下或肌肉注射MTX的所有随机对照试验(RCTs)。检索截止到2022年6月20日的MEDLINE、EMBASE和CENTRAL数据库。这个SR登记在普洛斯彼罗。结果:39项随机对照试验存在高偏倚风险。试验剂量仅在3个随机对照试验中给出。在随机对照试验中,MTX的起始剂量通常为7.5 mg/周(n = 13)。在AgEv中,MTX的起始剂量大多为15mg /周(n = 5)。一项指南建议使用试验剂量,而在其他综合证据中,没有提到甚至不鼓励使用试验剂量。结论:甲氨蝶呤治疗牛皮癣缺乏高质量的证据,现有数据也存在异质性。
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引用次数: 1
Efficacy and safety of lasers in treating syringomas: a review of the literature. 激光治疗丁香瘤的疗效和安全性:文献综述。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2127307
Mohammed Saud Alsaidan

Syringomas are benign adnexal neoplasms that may induce psychological stress when they are large or disfiguring or present in delicate regions such as the periorbital area. Despite the availability of various lasers for syringomas, no consensus has been established on the optimal laser setting and side effects of these therapies. The current review aims at understanding the efficacy and safety of various laser therapies available for the treatment of syringomas. A literature search was carried out using PubMed and Ovid databases for articles published from Jan 2000 through Mar 2022. Screening the eligible articles yielded 27 studies, comprising clinical studies, case series, and case reports, which were included in this review. The CO2 laser is the most widely used ablative laser therapy but is usually associated with adverse events. Pinhole and multiple drilling methods using CO2 laser yielded excellent cosmetic results with minimal adverse effects. Fractional lasers reduced the downtime and complications compared to non-fractionated ones. Non-ablative fractional lasers could be advantageous in terms of easy operation, minimal side effects and moderate recovery period compared with ablative lasers. Large clinical trials are needed to generate strong evidence to guide clinicians in choosing the most appropriate laser therapy for syringoma treatment.

性腺瘤是一种良性的附件肿瘤,当其体积较大、毁容或出现在如眶周等敏感区域时,可引起心理压力。尽管有各种各样的激光治疗丁香瘤,但在最佳激光设置和这些治疗的副作用方面还没有达成共识。目前的回顾旨在了解各种激光疗法的有效性和安全性,可用于治疗注射器瘤。使用PubMed和Ovid数据库对2000年1月至2022年3月发表的文章进行文献检索。筛选符合条件的文章产生27项研究,包括临床研究、病例系列和病例报告,纳入本综述。CO2激光是最广泛使用的烧蚀激光治疗,但通常与不良事件相关。使用CO2激光的针孔和多种钻孔方法产生了极好的美容效果,副作用最小。与非分馏激光器相比,分馏激光器减少了停机时间和并发症。与烧蚀激光相比,非烧蚀分数激光具有操作简单、副作用小、恢复期短等优点。需要大规模的临床试验来提供强有力的证据,以指导临床医生选择最合适的激光治疗方法来治疗注射器瘤。
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引用次数: 2
Psoriasis: is it a risk factor for cardiovascular diseases? 牛皮癣:是心血管疾病的危险因素吗?
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2112137
Hesham Nada, Attef Elakhrass, Neven Ahmad, Mohamed Refaat

Background/objectives: Psoriasis, newly considered as a systemic inflammatory condition, has a high prevalence of cardiovascular diseases (CVDs), including atherosclerosis and myocardial infarction. Measurement of carotid artery intima-media thickness (C-IMT) represents a noninvasive diagnostic tool for predicting cardiovascular disorders. We aimed to determine if psoriatic patients have an increased risk for the development of cardiovascular disorders by assessment of the presence of subclinical atherosclerosis in psoriasis patients.

Methods: Forty adult psoriatic patients and 40 matched healthy controls were selected in this study. All participants were subjected to full history, examination, assessment of the severity of psoriasis using psoriasis area and severity index (PASI) score, measuring serum lipid profile (cholesterol, low density lipoprotein (LDL) and triglycerides) and C-IMT.

Results: Psoriatic patients showed significantly higher serum lipid profile findings and C-IMT. There was a positive statistically significant correlation between C-IMT and each of age of the patients (r = 0.760, p<.001) and severity of psoriasis (PASI score).

Conclusions: There is increased susceptibility to CVDs in psoriatic patients represented by increased incidence of subclinical atherosclerosis and dyslipidemia in our patients.

背景/目的:银屑病最近被认为是一种全身性炎症疾病,其心血管疾病(cvd)的患病率很高,包括动脉粥样硬化和心肌梗死。测量颈动脉内膜-中膜厚度(C-IMT)是一种预测心血管疾病的无创诊断工具。我们的目的是通过评估银屑病患者亚临床动脉粥样硬化的存在来确定银屑病患者发生心血管疾病的风险是否增加。方法:选取40例成年银屑病患者和40例健康对照。所有参与者都接受了完整的病史,检查,使用牛皮癣面积和严重程度指数(PASI)评分评估牛皮癣的严重程度,测量血脂(胆固醇,低密度脂蛋白(LDL)和甘油三酯)和C-IMT。结果:银屑病患者血清脂质谱和C-IMT均明显增高。C-IMT与患者各年龄段的相关性有统计学意义(r = 0.760)。结论:银屑病患者对心血管疾病的易感性增加,表现为亚临床动脉粥样硬化和血脂异常的发生率增加。
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引用次数: 0
The Koo-Brownstone staging system as a tool to assist in the management of patients with a possible diagnosis of dermatological delusions: an experts suggestion. Koo-Brownstone分期系统作为一种工具,以协助管理可能诊断为皮肤病妄想的患者:专家建议。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2112548
Nicholas Brownstone, John Koo

Background: Delusional infestation (DI) is one of the most challenging situations dermatologists and other dermatology providers may face in their practice. Dermatologists must know how to properly communicate with these patients. The process of acquiring delusional states can be a gradual development and not all delusional patients in dermatology are the same.

Objective: The objective of this manuscript is to introduce the 'Koo-Brownstone Staging System' for Delusional Infestation (Morgellons disease) with the goal of improving communication and management for these patients.

Methods: This staging system has been derived based on more than three decades of experience of the senior author supported by additional years of experience of the first author.

Results: The following stages are presented and explained: formication only (stage 1), overvalued ideation of parasitosis (stage 2), pre-delusional (stage 3), delusional (stage 4) and terminally delusional (stage 5).

Limitations: This staging system has been derived based on expert clinical experience rather than a direct reporting from this patient population themselves.

Conclusions: This staging system will enhance awareness on the part of the health providers to enable them to categorize a given patient, which becomes critical in optimizing communications and management.

背景:妄想感染(DI)是皮肤科医生和其他皮肤科医生在实践中可能面临的最具挑战性的情况之一。皮肤科医生必须知道如何正确地与这些病人沟通。获得妄想状态的过程可以是一个渐进的发展,并不是所有的皮肤病妄想患者都是一样的。目的:本文旨在介绍妄想性感染(Morgellons病)的“Koo-Brownstone分期系统”,以改善对这些患者的沟通和管理。方法:这个分期系统是根据资深作者三十多年的经验和第一作者多年的经验推导出来的。结果:提出并解释了以下阶段:仅形成阶段(第1阶段),寄生虫病的高估概念(第2阶段),妄想前期(第3阶段),妄想(第4阶段)和晚期妄想(第5阶段)。局限性:该分期系统是根据专家临床经验推导出来的,而不是直接来自该患者群体自己的报告。结论:该分期系统将提高卫生服务提供者的意识,使他们能够对给定的患者进行分类,这对于优化沟通和管理至关重要。
{"title":"The Koo-Brownstone staging system as a tool to assist in the management of patients with a possible diagnosis of dermatological delusions: an experts suggestion.","authors":"Nicholas Brownstone,&nbsp;John Koo","doi":"10.1080/09546634.2022.2112548","DOIUrl":"https://doi.org/10.1080/09546634.2022.2112548","url":null,"abstract":"<p><strong>Background: </strong>Delusional infestation (DI) is one of the most challenging situations dermatologists and other dermatology providers may face in their practice. Dermatologists must know how to properly communicate with these patients. The process of acquiring delusional states can be a gradual development and not all delusional patients in dermatology are the same.</p><p><strong>Objective: </strong>The objective of this manuscript is to introduce the 'Koo-Brownstone Staging System' for Delusional Infestation (Morgellons disease) with the goal of improving communication and management for these patients.</p><p><strong>Methods: </strong>This staging system has been derived based on more than three decades of experience of the senior author supported by additional years of experience of the first author.</p><p><strong>Results: </strong>The following stages are presented and explained: formication only (stage 1), overvalued ideation of parasitosis (stage 2), pre-delusional (stage 3), delusional (stage 4) and terminally delusional (stage 5).</p><p><strong>Limitations: </strong>This staging system has been derived based on expert clinical experience rather than a direct reporting from this patient population themselves.</p><p><strong>Conclusions: </strong>This staging system will enhance awareness on the part of the health providers to enable them to categorize a given patient, which becomes critical in optimizing communications and management.</p>","PeriodicalId":15639,"journal":{"name":"Journal of Dermatological Treatment","volume":"33 8","pages":"3199-3201"},"PeriodicalIF":2.9,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10409102","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Anti-drug antibodies of IL-17 inhibitors for psoriasis: a systematic review. 银屑病IL-17抑制剂的抗药抗体:系统综述。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2114288
Alexandra Norden, Aislyn Oulee, Leena Munawar, Sogol Stephanie Javadi, George Han, Jashin J Wu

Biologics may elicit the production of anti-drug antibodies (ADAs), the clinical significance of which is not fully understood. ADA development in psoriasis patients on IL-17 inhibitors was evaluated by incidence, impact on efficacy, and relationship with adverse events. We systematically searched PubMed, Cochrane, and Embase databases, identifying 456 references. Seventeen studies met inclusion criteria. ADA incidence was: 0% to 5.5% (secukinumab), 11% to 19.4% (ixekizumab), 0% to 3.3% (brodalumab), and 19% to 39% (bimekizumab). Neutralizing antibody incidence was: 0% to 1.5% (secukinumab), 0% to 3.5% (ixekizumab), and 0% (brodalumab). ADA presence alone with secukinumab, ixekizumab, and bimekizumab did not impact drug efficacy. Brodalumab was the only one of the IL-17 inhibitors, which showed a reduction in efficacy in ADA + patients. In one analysis, high ADA titers to ixekizumab were associated with diminished treatment response. ADAs to secukinumab and bimekizumab were not associated with adverse events. There were limited data on ADAs and safety with ixekizumab or brodalumab. Overall, when monitoring patients on secukinumab, ADAs, titers, and the presence of neutralizing antibodies were not prognostic of outcomes. However, monitoring for ADAs with brodalumab and measuring titers with ixekizumab may be of value clinically.

生物制剂可能引起抗药物抗体(ADAs)的产生,其临床意义尚不完全清楚。使用IL-17抑制剂的银屑病患者ADA的发展通过发生率、疗效影响以及与不良事件的关系进行评估。我们系统地检索了PubMed、Cochrane和Embase数据库,确定了456篇参考文献。17项研究符合纳入标准。ADA的发生率为:0% - 5.5% (secukinumab), 11% - 19.4% (ixekizumab), 0% - 3.3% (brodalumab), 19% - 39% (bimekizumab)。中和抗体发生率为:0% - 1.5% (secukinumab), 0% - 3.5% (ixekizumab)和0% (brodalumab)。单独使用secukinumab、ixekizumab和bimekizumab的ADA不影响药物疗效。Brodalumab是唯一一种IL-17抑制剂,在ADA +患者中显示疗效降低。在一项分析中,对ixekizumab的高ADA滴度与治疗反应降低相关。舒金单抗和比美珠单抗的ADAs与不良事件无关。关于ADAs和ixekizumab或brodalumab安全性的数据有限。总的来说,当使用secukinumab监测患者时,ADAs、滴度和中和抗体的存在并不是预后的预测因素。然而,用brodalumab监测ADAs和用ixekizumab测量滴度可能在临床上有价值。
{"title":"Anti-drug antibodies of IL-17 inhibitors for psoriasis: a systematic review.","authors":"Alexandra Norden,&nbsp;Aislyn Oulee,&nbsp;Leena Munawar,&nbsp;Sogol Stephanie Javadi,&nbsp;George Han,&nbsp;Jashin J Wu","doi":"10.1080/09546634.2022.2114288","DOIUrl":"https://doi.org/10.1080/09546634.2022.2114288","url":null,"abstract":"<p><p>Biologics may elicit the production of anti-drug antibodies (ADAs), the clinical significance of which is not fully understood. ADA development in psoriasis patients on IL-17 inhibitors was evaluated by incidence, impact on efficacy, and relationship with adverse events. We systematically searched PubMed, Cochrane, and Embase databases, identifying 456 references. Seventeen studies met inclusion criteria. ADA incidence was: 0% to 5.5% (secukinumab), 11% to 19.4% (ixekizumab), 0% to 3.3% (brodalumab), and 19% to 39% (bimekizumab). Neutralizing antibody incidence was: 0% to 1.5% (secukinumab), 0% to 3.5% (ixekizumab), and 0% (brodalumab). ADA presence alone with secukinumab, ixekizumab, and bimekizumab did not impact drug efficacy. Brodalumab was the only one of the IL-17 inhibitors, which showed a reduction in efficacy in ADA + patients. In one analysis, high ADA titers to ixekizumab were associated with diminished treatment response. ADAs to secukinumab and bimekizumab were not associated with adverse events. There were limited data on ADAs and safety with ixekizumab or brodalumab. Overall, when monitoring patients on secukinumab, ADAs, titers, and the presence of neutralizing antibodies were not prognostic of outcomes. However, monitoring for ADAs with brodalumab and measuring titers with ixekizumab may be of value clinically.</p>","PeriodicalId":15639,"journal":{"name":"Journal of Dermatological Treatment","volume":"33 8","pages":"3080-3085"},"PeriodicalIF":2.9,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10414710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Brodalumab efficacy in bio-naïve psoriasis patients: real-life experience of 202 subjects up to 48 weeks. Brodalumab对bio-naïve牛皮癣患者的疗效:202名受试者长达48周的真实体验
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2125265
Luca Mastorino, C Cariti, S Susca, S Boskovic, C Aquino, M Ortoncelli, E Stroppiana, A Verrone, P Dapavo, P Quaglino, Simone Ribero
Interleukin-17 (IL-17) is central in the pathogenesis of psoriasis (1). Brodalumab was approved in Europe in 2017, and its blockade of IL-17 receptor A provides, in clinical trials, quick onset of action and long-term maintenance of treatment response with a favorable safety profile (2,3). Data regarding real-life use are limited (4–6). We retrospectively assessed efficacy and safety of brodalumab in moderate to severe psoriasis patients attending the Dermatology Clinic of the Turin University Hospital for up to 48weeks. Patients received subcutaneous brodalumab 210mg every 2weeks after the administration of 210mg every week for the first 3weeks. Disease severity at baseline was measured by the Psoriasis Area Severity Index (PASI); PASI improvement of 90% (PASI90) and 100% (PASI100) was recorded at 12, 24, and 48weeks. DLQI response rates were collected at baseline and after 48weeks of treatment. Among 1635 patients on biologics attending our clinic, 202 received brodalumab (Table 1). At week 12, 125 (68%) and 97 (53%) patients achieved PASI90 and PASI100, respectively. At week 24, 93 patients (77%) and 111 (65%) achieved PASI90 and PASI100, respectively. At week 48, 32 patients (78%) achieved PASI90 response, while 39 (64%) had complete clearance. Between baseline and week 48, DLQI improved from a mean of 13.8 to 1.3 (p< .001) and PASI improved from 23.3 to 2.2 (p< .001) respectively). Obesity did not seem to reduce the efficacy or time to onset of action of brodalumab since no difference in efficacy was observed between patients with a BMI above or below 30. No significant differences in efficacy were detected at the different time points between patients with and without joint involvement (Figure 1). Bio-naïve patients improved faster than bio-experienced patients in the first weeks of treatment and at every time point. At week 12, the mean PASI in the bio-naïve population was lower than in the bio-experienced (1.56 vs 2.47; p1⁄4 .045), and more patients achieved PASI 90 and PASI <3 (76% vs 56%; p1⁄4 .004 and 86% vs 69%; p1⁄4 .005). At week 24, more bio-naïve patients than bio-experienced patients achieved PASI90 (84% vs 67%, p1⁄4 .021). Forty-nine patients reported side effects, the most frequent of which were arthralgia (15 patients) in patients without joint involvement at baseline and asthenia (10 patients). Two patients discontinued treatment due to reported side effects, one due to joint pain and one due to a major dental abscess resistant to multiple antibiotic therapies. Brodalumab rapidly improves psoriasis in the first few weeks of treatment, particularly in bio-naïve patients, which is in line with the results of registration studies and previous real-life experience (3,5,6). Performance in bio-experienced patients is also good, as previously reported (5,6). Although not approved in the treatment of psoriatic arthritis, joint involvement does not appear to affect the response to therapy.
{"title":"Brodalumab efficacy in bio-naïve psoriasis patients: real-life experience of 202 subjects up to 48 weeks.","authors":"Luca Mastorino,&nbsp;C Cariti,&nbsp;S Susca,&nbsp;S Boskovic,&nbsp;C Aquino,&nbsp;M Ortoncelli,&nbsp;E Stroppiana,&nbsp;A Verrone,&nbsp;P Dapavo,&nbsp;P Quaglino,&nbsp;Simone Ribero","doi":"10.1080/09546634.2022.2125265","DOIUrl":"https://doi.org/10.1080/09546634.2022.2125265","url":null,"abstract":"Interleukin-17 (IL-17) is central in the pathogenesis of psoriasis (1). Brodalumab was approved in Europe in 2017, and its blockade of IL-17 receptor A provides, in clinical trials, quick onset of action and long-term maintenance of treatment response with a favorable safety profile (2,3). Data regarding real-life use are limited (4–6). We retrospectively assessed efficacy and safety of brodalumab in moderate to severe psoriasis patients attending the Dermatology Clinic of the Turin University Hospital for up to 48weeks. Patients received subcutaneous brodalumab 210mg every 2weeks after the administration of 210mg every week for the first 3weeks. Disease severity at baseline was measured by the Psoriasis Area Severity Index (PASI); PASI improvement of 90% (PASI90) and 100% (PASI100) was recorded at 12, 24, and 48weeks. DLQI response rates were collected at baseline and after 48weeks of treatment. Among 1635 patients on biologics attending our clinic, 202 received brodalumab (Table 1). At week 12, 125 (68%) and 97 (53%) patients achieved PASI90 and PASI100, respectively. At week 24, 93 patients (77%) and 111 (65%) achieved PASI90 and PASI100, respectively. At week 48, 32 patients (78%) achieved PASI90 response, while 39 (64%) had complete clearance. Between baseline and week 48, DLQI improved from a mean of 13.8 to 1.3 (p< .001) and PASI improved from 23.3 to 2.2 (p< .001) respectively). Obesity did not seem to reduce the efficacy or time to onset of action of brodalumab since no difference in efficacy was observed between patients with a BMI above or below 30. No significant differences in efficacy were detected at the different time points between patients with and without joint involvement (Figure 1). Bio-naïve patients improved faster than bio-experienced patients in the first weeks of treatment and at every time point. At week 12, the mean PASI in the bio-naïve population was lower than in the bio-experienced (1.56 vs 2.47; p1⁄4 .045), and more patients achieved PASI 90 and PASI <3 (76% vs 56%; p1⁄4 .004 and 86% vs 69%; p1⁄4 .005). At week 24, more bio-naïve patients than bio-experienced patients achieved PASI90 (84% vs 67%, p1⁄4 .021). Forty-nine patients reported side effects, the most frequent of which were arthralgia (15 patients) in patients without joint involvement at baseline and asthenia (10 patients). Two patients discontinued treatment due to reported side effects, one due to joint pain and one due to a major dental abscess resistant to multiple antibiotic therapies. Brodalumab rapidly improves psoriasis in the first few weeks of treatment, particularly in bio-naïve patients, which is in line with the results of registration studies and previous real-life experience (3,5,6). Performance in bio-experienced patients is also good, as previously reported (5,6). Although not approved in the treatment of psoriatic arthritis, joint involvement does not appear to affect the response to therapy.","PeriodicalId":15639,"journal":{"name":"Journal of Dermatological Treatment","volume":"33 8","pages":"3211-3213"},"PeriodicalIF":2.9,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10433466","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Inflamed actinic keratoses as a biomarker in repositioning of chemotherapeutics: a systematic review and meta-analysis. 炎症性光化性角化病作为化疗药物重新定位的生物标志物:一项系统综述和荟萃分析。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2131298
Špela Šuler Baglama, Irena Peteln, Gregor B E Jemec

Background: Inflammation of actinic keratoses (AK) was originally described with systemic 5-fluorouracil, and led to the development of topical fluorouracil. Similar observations using different chemotherapeutics may point to other drugs with a potential for repositioning.

Objective: This systematic review aims to evaluate chemotherapeutic agents linked to inflammation-induced cure of AK.

Methods: This systematic review was registered in PROSPERO (CRD42022346168) and followed PRISMA guidelines. A comprehensive literature search for eligible original articles written in English and published in peer-reviewed journals until July 13, 2022 was conducted in MEDLINE and Embase.

Results: 28 articles met inclusion criteria accounting for 36 patients (mean age 68.4 ± 8.3 years) with inflamed AK, exposed to 21 different chemotherapeutic agents - 21/36 (58.3%) received monotherapy and 15/36 (41.7%) received multidrug combinations. Regression was complete in 13/28 (46.4%) and partial in 14/28 (50.0%) of inflamed AK. Cure rates of inflamed AK in multidrug combinations were not superior to monotherapies (p = .252), leading to the observation that the majority of the former (14/15; 93.3%) encompassed one of five chemotherapeutic agents linked to AK inflammation also as a monotherapy.

Conclusion: Overall, inflammation partially/completely cured AK in 96.4% of patients (27/28). Taxanes, pemetrexed, and doxorubicin might have the potential for the management of AK.

背景:光化性角化病(AK)的炎症最初是用全身5-氟尿嘧啶来描述的,并导致了局部氟尿嘧啶的发展。使用不同化疗药物的类似观察结果可能指向其他具有重新定位潜力的药物。目的:本系统综述旨在评价化疗药物与炎症诱导的AK治愈相关。方法:本系统评价在PROSPERO注册(CRD42022346168),遵循PRISMA指南。在MEDLINE和Embase中对2022年7月13日之前发表在同行评审期刊上的符合条件的英文原创文章进行了全面的文献检索。结果:28篇文章符合纳入标准,36例患者(平均年龄68.4±8.3岁)炎症性AK,接受21种不同的化疗药物,其中21/36(58.3%)接受单一治疗,15/36(41.7%)接受多药联合治疗。炎性AK在13/28(46.4%)完全回归,14/28(50.0%)部分回归。多药联合治疗炎症性AK的治愈率并不优于单药治疗(p = .252),导致观察到前者的大多数(14/15;93.3%)包括与AK炎症相关的五种化疗药物中的一种,也作为单一疗法。结论:总体而言,炎症部分/完全治愈AK的患者占96.4%(27/28)。紫杉烷、培美曲塞和阿霉素可能具有治疗AK的潜力。
{"title":"Inflamed actinic keratoses as a biomarker in repositioning of chemotherapeutics: a systematic review and meta-analysis.","authors":"Špela Šuler Baglama,&nbsp;Irena Peteln,&nbsp;Gregor B E Jemec","doi":"10.1080/09546634.2022.2131298","DOIUrl":"https://doi.org/10.1080/09546634.2022.2131298","url":null,"abstract":"<p><strong>Background: </strong>Inflammation of actinic keratoses (AK) was originally described with systemic 5-fluorouracil, and led to the development of topical fluorouracil. Similar observations using different chemotherapeutics may point to other drugs with a potential for repositioning.</p><p><strong>Objective: </strong>This systematic review aims to evaluate chemotherapeutic agents linked to inflammation-induced cure of AK.</p><p><strong>Methods: </strong>This systematic review was registered in PROSPERO (CRD42022346168) and followed PRISMA guidelines. A comprehensive literature search for eligible original articles written in English and published in peer-reviewed journals until July 13, 2022 was conducted in MEDLINE and Embase.</p><p><strong>Results: </strong>28 articles met inclusion criteria accounting for 36 patients (mean age 68.4 ± 8.3 years) with inflamed AK, exposed to 21 different chemotherapeutic agents - 21/36 (58.3%) received monotherapy and 15/36 (41.7%) received multidrug combinations. Regression was complete in 13/28 (46.4%) and partial in 14/28 (50.0%) of inflamed AK. Cure rates of inflamed AK in multidrug combinations were not superior to monotherapies (<i>p</i> = .252), leading to the observation that the majority of the former (14/15; 93.3%) encompassed one of five chemotherapeutic agents linked to AK inflammation also as a monotherapy.</p><p><strong>Conclusion: </strong>Overall, inflammation partially/completely cured AK in 96.4% of patients (27/28). Taxanes, pemetrexed, and doxorubicin might have the potential for the management of AK.</p>","PeriodicalId":15639,"journal":{"name":"Journal of Dermatological Treatment","volume":"33 8","pages":"3136-3142"},"PeriodicalIF":2.9,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10433775","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Cost-utility study of home-based cryotherapy device for wart treatment: a randomized, controlled, and investigator-blinded trial. 家庭冷冻治疗装置治疗疣的成本-效用研究:一项随机、对照、研究者盲法试验。
IF 2.9 4区 医学 Q1 Medicine Pub Date : 2022-12-01 DOI: 10.1080/09546634.2022.2114782
Nattanichcha Kulthanachairojana, Suthira Taychakhoonavudh, Kanokvalai Kulthanan, Sumanas Bunyaratavej, Sasima Eimpunth, Bawonpak Pongkittilar, Suthasanee Prasertsook, Supisara Wongdama, Charussri Leeyaphan

Background: Cryotherapy is typically performed by physicians. No cost-utility studies of home-based cryotherapy have been reported.

Objectives: To study the cost utility of home-based cryotherapy devices and in-hospital liquid nitrogen therapy for cutaneous warts.

Materials and methods: This randomized, controlled, investigator-blinded trial was carried out on patients with cutaneous warts. Participants were randomly assigned to two groups: home-based cryotherapy and in-hospital liquid nitrogen therapy. Clinical examinations were conducted at baseline and monthly until cure, and outcomes (cure rate, side effects, total costs, and quality of life) were compared. A cost-utility analysis was performed.

Results: Nineteen of 22 patients completed the treatment and were analyzed. The efficacy of home-based cryotherapy and in-hospital therapy was 72.8% and 64.3%, respectively. Side effects (pain, redness, and burning) were observed. The mean numbers of medical visits were 2.83 for home-based therapy and 3.30 for in-hospital therapy. The total costs for home-based therapy and the in-hospital therapy were US $76.03 and $100.45, respectively. The home-based therapy had 0.2297 quality-adjusted life years, slightly higher than the corresponding value of 0.2254 for in-hospital therapy.

Conclusions: Home-based cryotherapy devices are a cost-saving strategy with similar efficacy to in-hospital liquid nitrogen therapy.

背景:冷冻治疗通常由医生进行。没有关于家庭冷冻疗法的成本效用研究的报道。目的:探讨家用冷冻治疗装置和住院液氮治疗皮肤疣的成本效益。材料和方法:这项随机、对照、研究者盲法试验在皮肤疣患者中进行。参与者被随机分为两组:家庭冷冻疗法和医院液氮疗法。在基线和每月进行临床检查,直到治愈,并比较结果(治愈率,副作用,总成本和生活质量)。进行了成本效用分析。结果:22例患者中有19例完成治疗并进行分析。家庭冷冻治疗和住院冷冻治疗的有效率分别为72.8%和64.3%。观察了副作用(疼痛、发红、灼烧)。家庭治疗的平均诊疗次数为2.83次,住院治疗的平均诊疗次数为3.30次。家庭治疗和住院治疗的总费用分别为76.03美元和100.45美元。家庭治疗的质量调整生命年为0.2297,略高于住院治疗的相应值0.2254。结论:家庭冷冻装置是一种节省成本的策略,其效果与医院液氮治疗相似。
{"title":"Cost-utility study of home-based cryotherapy device for wart treatment: a randomized, controlled, and investigator-blinded trial.","authors":"Nattanichcha Kulthanachairojana,&nbsp;Suthira Taychakhoonavudh,&nbsp;Kanokvalai Kulthanan,&nbsp;Sumanas Bunyaratavej,&nbsp;Sasima Eimpunth,&nbsp;Bawonpak Pongkittilar,&nbsp;Suthasanee Prasertsook,&nbsp;Supisara Wongdama,&nbsp;Charussri Leeyaphan","doi":"10.1080/09546634.2022.2114782","DOIUrl":"https://doi.org/10.1080/09546634.2022.2114782","url":null,"abstract":"<p><strong>Background: </strong>Cryotherapy is typically performed by physicians. No cost-utility studies of home-based cryotherapy have been reported.</p><p><strong>Objectives: </strong>To study the cost utility of home-based cryotherapy devices and in-hospital liquid nitrogen therapy for cutaneous warts.</p><p><strong>Materials and methods: </strong>This randomized, controlled, investigator-blinded trial was carried out on patients with cutaneous warts. Participants were randomly assigned to two groups: home-based cryotherapy and in-hospital liquid nitrogen therapy. Clinical examinations were conducted at baseline and monthly until cure, and outcomes (cure rate, side effects, total costs, and quality of life) were compared. A cost-utility analysis was performed.</p><p><strong>Results: </strong>Nineteen of 22 patients completed the treatment and were analyzed. The efficacy of home-based cryotherapy and in-hospital therapy was 72.8% and 64.3%, respectively. Side effects (pain, redness, and burning) were observed. The mean numbers of medical visits were 2.83 for home-based therapy and 3.30 for in-hospital therapy. The total costs for home-based therapy and the in-hospital therapy were US $76.03 and $100.45, respectively. The home-based therapy had 0.2297 quality-adjusted life years, slightly higher than the corresponding value of 0.2254 for in-hospital therapy.</p><p><strong>Conclusions: </strong>Home-based cryotherapy devices are a cost-saving strategy with similar efficacy to in-hospital liquid nitrogen therapy.</p>","PeriodicalId":15639,"journal":{"name":"Journal of Dermatological Treatment","volume":"33 8","pages":"3165-3169"},"PeriodicalIF":2.9,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10401641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Dermatological Treatment
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