JAK1抑制剂治疗特应性皮炎:药代动力学研究的重点。

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Expert Opinion on Drug Metabolism & Toxicology Pub Date : 2023-07-01 Epub Date: 2023-09-11 DOI:10.1080/17425255.2023.2256227
Hannah Kopelman, Christina Kontzias, Christopher Alihosseni, Steven R Feldman
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引用次数: 0

摘要

引言:特应性皮炎(AD)与生活质量下降、抑郁和焦虑有关,因此应优先考虑有效和安全的治疗。我们将重点关注用于治疗AD的JAK1抑制剂的安全性、有效性和药代动力学。涵盖的领域:在这篇综述中,讨论了JAK1抑制剂治疗特应性皮炎的药效学、药代动力学、安全性和有效性。数据是通过搜索ClinicalTrials.gov、PubMed和Google Scholar获得的。2012年1月至2023年3月期间的文章被考虑纳入。专家意见:鉴于JAK抑制剂的罕见但严重的黑匣子警告,患者和提供者可能对开始治疗感到厌倦。在这些情况下,临床医生可能会权衡此类治疗的风险和益处。风险是相对的,虽然用JAK抑制剂治疗AD有风险,但未经治疗或治疗不足的AD也有风险,包括感染和精神、身体和心理社会功能受损。虽然JAK1抑制剂似乎是安全的,但它们最近才在2022年1月被批准用于AD,还需要更多的长期安全性数据。我们希望在未来看到美国食品药品监督管理局对这些药物、新配方的更多批准,以及更多的安全性和有效性数据。
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JAK1 inhibitors for the treatment of atopic dermatitis: a focus on pharmacokinetic considerations.

Introduction: Atopic dermatitis (AD) is associated with reduced quality of life, depression, and anxiety, making efficacious and safe treatments a priority. We will focus on the safety, efficacy, and pharmacokinetics of JAK1 inhibitors used in the treatment of AD.

Areas covered: In this review, the pharmacodynamics, pharmacokinetics, safety, and efficacy of JAK1 inhibitors for the treatment of atopic dermatitis are discussed. The data was obtained by searching ClinicalTrials.gov, PubMed, and Google Scholar. Articles between January 2012 and March 2023 were considered for inclusion.

Expert opinion: Given the rare, but serious black box warnings with JAK inhibitors, patients and providers may be weary of initiating treatment. In these instances, clinicians may weigh the risks and benefits of treatment with this class. Risk is relative, and while there are risks to treating AD with JAK inhibitors, there are also risks to untreated or undertreated AD, including infection and impairments in mental, physical, and psychosocial function. While JAK1 inhibitors appear to be safe, they were only recently approved for AD in January 2022, and more long-term safety data is needed. We expect to see additional FDA approval of these drugs, new formulations, and more safety and efficacy data in the future.

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来源期刊
Expert Opinion on Drug Metabolism & Toxicology
Expert Opinion on Drug Metabolism & Toxicology 医学-生化与分子生物学
CiteScore
7.90
自引率
2.30%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Drug Metabolism & Toxicology (ISSN 1742-5255 [print], 1744-7607 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on all aspects of ADME-Tox. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering metabolic, pharmacokinetic and toxicological issues relating to specific drugs, drug-drug interactions, drug classes or their use in specific populations; issues relating to enzymes involved in the metabolism, disposition and excretion of drugs; techniques involved in the study of drug metabolism and toxicology; novel technologies for obtaining ADME-Tox data. Drug Evaluations reviewing the clinical, toxicological and pharmacokinetic data on a particular drug. The audience consists of scientists and managers in the pharmaceutical industry, pharmacologists, clinical toxicologists and related professionals.
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