Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adv Exp Med Biol. 2020;1244:235-246. doi: 10.1007/978-3-030-41008-7_11.
Due to the novelty of immune checkpoint inhibitors, their cutaneous adverse events (AEs) have only been recently characterized. This, along with the substantial rate of cutaneous reactions, has left many clinicians without sufficient familiarity to diagnose and treat cutaneous AEs. Pruritus and rash are among the top five immune-related AEs reported in clinical trials for this class of therapy. Incidence varies between 35 and 50% for cutaneous AEs among the eight FDA-approved drugs. Although only 2% are reported as grade 3 or 4 events, the impact on quality of life can be significant for these patients and is best described and most severe in ipilimumab trials. Of ipilimumab patients, 43.5% have a cutaneous AE and, at our institution, 20% of them had a dose interruption as a result. This means potentially 9% of patients have dose interruption of ipilimumab because of their cutaneous AEs. In the following chapter, we review the categories of these drugs, common cutaneous effects, their grading, and management options.
由于免疫检查点抑制剂具有新颖性,其皮肤不良反应 (AE) 最近才被描述。再加上皮肤反应的发生率很高,许多临床医生对诊断和治疗皮肤不良反应并不熟悉。瘙痒和皮疹是这类治疗药物临床试验中报告的前五种免疫相关不良反应之一。在 FDA 批准的八种药物中,皮肤不良反应的发生率在 35%至 50%之间。尽管只有 2%被报告为 3 级或 4 级事件,但这些患者的生活质量受到的影响可能很大,在 ipilimumab 试验中描述得最为详细,也最为严重。在接受 ipilimumab 治疗的患者中,有 43.5%出现皮肤不良反应,在我们的机构中,有 20%的患者因此中断了治疗。这意味着,由于皮肤不良反应,ipilimumab 的剂量中断率可能高达 9%。在接下来的章节中,我们将回顾这些药物的类别、常见的皮肤作用、分级以及管理选择。