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免疫检查点抑制剂的皮肤不良反应:皮肤毒性与免疫治疗

Dermatologic Reactions to Immune Checkpoint Inhibitors : Skin Toxicities and Immunotherapy.

机构信息

Oncodermatology, Institut Claudius REGAUD and Institut Universitaire du Cancer Toulouse Oncopole, 1 avenue Irène Joliot-Curie, 31059, Toulouse Cedex 9, France.

出版信息

Am J Clin Dermatol. 2018 Jun;19(3):345-361. doi: 10.1007/s40257-017-0336-3.

Abstract

The development of immune checkpoint inhibitors [monoclonal antibodies targeting cytotoxic T lymphocyte-associated antigen-4 (CTLA-4), programmed cell death protein 1 (PD-1) or programmed death ligand 1 (PD-L1)] represents a major breakthrough in cancer therapy. Although they present a favorable risk/benefit ratio, immune checkpoint blockade therapies have a very specific safety profile. Due to their unique mechanism of action, they entail a new spectrum of adverse events that are mostly immune related [immune-related adverse events (irAEs)], notably mediated by the triggering of cytotoxic CD4+/CD8+ T cell activation. Cutaneous toxicities appear to be one of the most prevalent irAEs, both with anti-PD-1 and anti-CTLA-4 agents or with the newly developed anti-PD-L1 agents, which corresponds to a class effect. They are observed in more than one-third of the treated patients, mainly in the form of a maculopapular rash (eczema-like spongiotic dermatitis) and pruritus. A wide range of other dermatologic manifestations can also occur, including lichenoid reactions, psoriasis, acneiform rashes, vitiligo-like lesions, autoimmune skin diseases (e.g., bullous pemphigoid, dermatomyositis, alopecia areata), sarcoidosis or nail and oral mucosal changes. In addition, the use of anti-CTLA-4 and anti-PD-1 therapies in combination is associated with the development of more frequent, more severe and earlier cutaneous irAEs compared to single agents. In most cases, these dysimmune dermatologic adverse events remain self-limiting and readily manageable. Early recognition and adequate management, however, are critical to prevent exacerbation of the lesions, to limit treatment interruption and to minimize quality of life impairment. This review describes the variable clinical and histopathologic aspects of dermatologic irAEs induced by immune checkpoint inhibitors. Appropriate treatment and counseling are also proposed, with a step-by-step approach for optimized management by both practicing oncologists and dermatologists.

摘要

免疫检查点抑制剂(靶向细胞毒性 T 淋巴细胞相关抗原-4(CTLA-4)、程序性细胞死亡蛋白 1(PD-1)或程序性死亡配体 1(PD-L1)的单克隆抗体)的开发代表了癌症治疗的重大突破。尽管它们具有良好的风险/获益比,但免疫检查点阻断疗法具有非常特殊的安全性特征。由于其独特的作用机制,它们引发了一系列新的不良反应,这些不良反应主要与免疫有关(免疫相关不良反应(irAEs)),特别是通过触发细胞毒性 CD4+/CD8+T 细胞激活。皮肤毒性似乎是最常见的 irAEs 之一,无论是抗 PD-1 还是抗 CTLA-4 药物,还是新开发的抗 PD-L1 药物,都存在这种情况,这是一种类效应。它们在超过三分之一的治疗患者中观察到,主要表现为斑丘疹(湿疹样海绵状皮炎)和瘙痒。也可能出现广泛的其他皮肤表现,包括苔藓样反应、银屑病、痤疮样皮疹、白癜风样病变、自身免疫性皮肤病(如大疱性类天疱疮、皮肌炎、斑秃)、结节病或指甲和口腔黏膜改变。此外,与单药治疗相比,抗 CTLA-4 和抗 PD-1 联合治疗与更频繁、更严重和更早出现的皮肤 irAEs 相关。在大多数情况下,这些免疫失调性皮肤不良反应仍然是自限性的,易于管理。然而,早期识别和充分管理对于预防病变恶化、限制治疗中断和最大限度地减少生活质量损害至关重要。这篇综述描述了免疫检查点抑制剂引起的皮肤 irAEs 的可变临床和组织病理学方面。还提出了适当的治疗和咨询建议,并提出了一种由肿瘤学家和皮肤科医生共同优化管理的逐步方法。

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