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与靶向治疗和生物制剂相关的药物诱导的结节病样反应。

Drug-Induced Sarcoid-like Reactions Associated to Targeted Therapies and Biologic Agents.

作者信息

Andolfi Federica, Caffarri Luca, Neviani Matilde, Rubini Silvia, Andrisani Dario, Gozzi Filippo, Beghé Bianca, Clini Enrico, Tonelli Roberto, Cerri Stefania

机构信息

Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, 41121 Modena, Italy.

Respiratory Disease Unit, University Hospital of Modena-Policlinico, 41124 Modena, Italy.

出版信息

Diagnostics (Basel). 2025 Jun 29;15(13):1658. doi: 10.3390/diagnostics15131658.

Abstract

: Sarcoidosis is a multisystem inflammatory disease characterized by the immune-mediated formation of non-necrotizing epithelioid granulomas. Several commonly used medications can induce similar granulomatous reactions, known as drug-induced sarcoid-like reactions (DISRs), which closely mimic sarcoidosis. Despite their specificity in targeting molecular pathways, certain therapies-particularly targeted treatments-have increasingly been linked to DISRs. : This narrative review was based on a PubMed search using the terms "SARCOID LIKE REACTION" and "DRUG". A cross-check was performed with "SARCOID" combined with each identified drug to identify misclassified cases. Drugs with limited evidence or weak pathogenetic plausibility were excluded, leaving only molecularly targeted therapies for consideration. Sources included case reports, case series, and reviews selected based on their clinical and scientific relevance, without any restrictions on time or language. : In light of the available data, five main pharmacological groups were found to be associated to DISR: immune checkpoint inhibitors, TNF-α antagonists, BRAF inhibitors, monoclonal antibodies, and miscellaneous agents. Each group has distinct mechanisms of action and clinical indications, which likely affect the frequency, presentation, and timing of DISRs. : Diagnosing DISRs is challenging, and a structured approach is crucial for differentiating them from other conditions. To support clinicians, we propose a diagnostic algorithm to guide decision-making in suspected cases. Management should be individualized, as most DISRs either resolve spontaneously or improve after the discontinuation of the causative drug. Important factors influencing therapeutic decisions include the severity of the underlying disease, the availability of alternative treatments, and the extent of DISR manifestations.

摘要

结节病是一种多系统炎症性疾病,其特征是免疫介导形成非坏死性上皮样肉芽肿。几种常用药物可诱发类似的肉芽肿反应,称为药物性结节病样反应(DISRs),与结节病极为相似。尽管某些疗法尤其是靶向治疗在分子途径靶向方面具有特异性,但它们与DISRs的关联却日益增加。

本叙述性综述基于PubMed搜索,搜索词为“SARCOID LIKE REACTION”和“DRUG”。将“SARCOID”与每种已识别药物相结合进行交叉核对,以识别误分类病例。证据有限或致病合理性较弱的药物被排除,仅考虑分子靶向疗法。资料来源包括病例报告、病例系列以及根据其临床和科学相关性选择的综述,对时间和语言没有任何限制。

根据现有数据,发现有五个主要药物类别与DISR相关:免疫检查点抑制剂、TNF-α拮抗剂、BRAF抑制剂、单克隆抗体和其他药物。每个类别都有不同的作用机制和临床适应症,这可能会影响DISRs的发生频率、表现形式和时间。

诊断DISRs具有挑战性,采用结构化方法对于将它们与其他病症区分开来至关重要。为了帮助临床医生,我们提出一种诊断算法,以指导疑似病例的决策。管理应个体化,因为大多数DISRs要么自行缓解,要么在停用致病药物后有所改善。影响治疗决策的重要因素包括基础疾病的严重程度、替代治疗的可用性以及DISR表现的程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44c6/12249406/e3a7d7e5572a/diagnostics-15-01658-g001.jpg

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