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Prevalence of psoriasis among adults in the US 2009-2010 and 2013-2014 National Health and Nutrition Examination Surveys.2009 - 2010年及2013 - 2014年美国国家健康与营养检查调查中成人银屑病的患病率。
J Am Acad Dermatol. 2021 Mar;84(3):767-769. doi: 10.1016/j.jaad.2020.10.035. Epub 2020 Oct 23.
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Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine.BNT162b2 mRNA 新冠病毒疫苗的安全性和有效性。
N Engl J Med. 2020 Dec 31;383(27):2603-2615. doi: 10.1056/NEJMoa2034577. Epub 2020 Dec 10.
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Effect of anti-tumor necrosis factor therapy on the risk of respiratory tract infections and related symptoms in patients with psoriasis-A meta-estimate of pivotal phase 3 trials relevant to decision making during the COVID-19 pandemic.抗肿瘤坏死因子疗法对银屑病患者呼吸道感染风险及相关症状的影响——COVID-19大流行期间与决策相关的关键3期试验的荟萃估计
J Am Acad Dermatol. 2021 Jan;84(1):161-163. doi: 10.1016/j.jaad.2020.08.095. Epub 2020 Aug 26.
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One-Year Pharmacovigilance Update of Brodalumab.布罗达单抗的一年药物警戒更新
J Drugs Dermatol. 2020 Aug 1;19(8):807-808. doi: 10.36849/JDD.2020.5138.
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The exposure to biologic and targeted synthetic disease-modifying antirheumatic drugs in pregnancy and lactation.孕期及哺乳期接触生物制剂和靶向合成改善病情抗风湿药的情况。
Postepy Dermatol Alergol. 2020 Jun;37(3):306-312. doi: 10.5114/ada.2020.96294. Epub 2020 Jul 14.
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RMD Open. 2020 Jul;6(2). doi: 10.1136/rmdopen-2020-001217.
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Multicentre, randomised, open-label, parallel-group study evaluating the efficacy and safety of ixekizumab versus adalimumab in patients with psoriatic arthritis naïve to biological disease-modifying antirheumatic drug: final results by week 52.多中心、随机、开放标签、平行组研究评估依奇珠单抗与阿达木单抗在生物疾病修正抗风湿药物初治的银屑病关节炎患者中的疗效和安全性:第 52 周的最终结果。
Ann Rheum Dis. 2020 Oct;79(10):1310-1319. doi: 10.1136/annrheumdis-2020-217372. Epub 2020 Jul 13.
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The risk of respiratory tract infections in patients with psoriasis treated with interleukin 23 pathway-inhibiting biologics: A meta-estimate of pivotal trials relevant to decision making during the COVID-19 pandemic.接受白细胞介素23通路抑制生物制剂治疗的银屑病患者发生呼吸道感染的风险:COVID-19大流行期间与决策相关的关键试验的荟萃估计。
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Combination treatment with secukinumab and dimethyl fumarate in a patient with psoriasis and recent diagnosis of multiple sclerosis.司库奇尤单抗与富马酸二甲酯联合治疗一名银屑病患者及近期诊断为多发性硬化症的病例
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伴有合并症和特殊人群的中重度银屑病的生物治疗算法:综述。

Biologic Treatment Algorithms for Moderate-to-Severe Psoriasis with Comorbid Conditions and Special Populations: A Review.

机构信息

College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA, USA.

School of Medicine, University of California, Riverside, CA, USA.

出版信息

Am J Clin Dermatol. 2021 Jul;22(4):425-442. doi: 10.1007/s40257-021-00603-w. Epub 2021 Apr 16.

DOI:10.1007/s40257-021-00603-w
PMID:33861409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8051287/
Abstract

The emergence of data from clinical trials of biologics, the approval of new biologics, and our improved understanding of psoriasis pathogenesis have increased the therapeutic possibilities for the treatment of moderate-to-severe psoriasis. Biologics currently approved for the treatment of psoriasis include tumor necrosis factor inhibitors, interleukin (IL)-17 inhibitors, ustekinumab (an IL-12/23 inhibitor), and IL-23 inhibitors. Data from clinical trials and studies of the safety and efficacy of biologics provide essential information for the personalization of patient care. We discuss the benefits and disadvantages of biologics as a first-line treatment choice, update treatment recommendations according to current evidence, and propose psoriasis treatment algorithms. Our discussion includes the following comorbid conditions: psoriatic arthritis, multiple sclerosis, congestive heart failure, inflammatory bowel disease, hepatitis B, nonmelanoma skin cancer, lymphoma, and latent tuberculosis. We make evidence-based treatment recommendations for special populations, including pediatric patients, patients with coronavirus 2019 (COVID-19), and pregnant and breastfeeding patients with psoriasis. Ultimately, individualized recommendations that consider patient preferences, disease severity, comorbid conditions, and additional risk factors should be offered to patients and updated as new trial data emerges.

摘要

生物制剂临床试验数据的出现、新型生物制剂的获批,以及我们对银屑病发病机制认识的提高,增加了中重度银屑病治疗的可能性。目前批准用于银屑病治疗的生物制剂包括肿瘤坏死因子抑制剂、白细胞介素(IL)-17 抑制剂、乌司奴单抗(一种 IL-12/23 抑制剂)和 IL-23 抑制剂。生物制剂临床试验和安全性及疗效研究的数据为患者个体化治疗提供了重要信息。我们讨论了生物制剂作为一线治疗选择的优缺点,根据现有证据更新治疗建议,并提出银屑病治疗方案。我们的讨论包括以下合并症:银屑病关节炎、多发性硬化症、充血性心力衰竭、炎症性肠病、乙型肝炎、非黑素瘤皮肤癌、淋巴瘤和潜伏性结核。我们针对特殊人群(包括儿科患者、2019 冠状病毒病(COVID-19)患者和患有银屑病的妊娠及哺乳期患者)提供了基于证据的治疗建议。最终,应根据患者偏好、疾病严重程度、合并症和其他风险因素向患者提供个体化建议,并在新的试验数据出现时进行更新。