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[免疫检查点抑制剂诱导的多种免疫相关不良事件——与血清白细胞介素-6水平升高相关的纳武单抗相关银屑病样皮炎]

[Varied immuno-related adverse events induced by immune-check point inhibitors - Nivolumab-associated psoriasiform dermatitis related with increased serum level of interleukin-6].

作者信息

Okiyama Naoko, Tanaka Ryota

机构信息

Department of Dermatology, Faculty of Medicine, University of Tsukuba.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(2):95-101. doi: 10.2177/jsci.40.95.

Abstract

Nivolumab is a standard recombinant antibody treatment for patients with malignant melanoma (MM), which functions as an immune checkpoint inhibitor by blocking the programmed cell death-1 (PD-1) pathway in T cells. However, it leads to various immune-related adverse events (irAEs), and also exacerbates underlying autoimmune diseases. Herein we report cases of MM with irAE. Case 1: A 69-year-old woman with MM developed destructive thyroiditis resulting in hypothyroidism after 3 doses of nivolumab, and had been treated with thyroid gland auxiliary therapy. Case 2: A 80-year-old man with MM developed an acute onset of hyperthyroidism after 4 doses of nivolumab. Case 3: A 85-year-old woman with MM developed polyradiculoneuropathy resulting in somatosensory disorder and muscle weakness after 2 doses of nivolumab, and had been treated with intravenous immunoglobulin and oral predonisolone (40 mg/day). Case 4: A 77-year-old man with MM developed psoriasiform dermatitis after local injections of IFN-β and 11 doses of nivolumab. Case 5: Case 2 also developed psoriasiform dermatitis. We analyzed serum levels of inflammatory cytokines in MM patients before/after treatments with nivolumab. All six patients who developed psoriasiform dermatitis with/without anamnesis of psoriasis after treatment with nivolumab, and all seven patients with other irAE exhibited increased serum IL-6 levels after nivolumab treatment, while decreased serum levels of IL-6 were observed in 5 of 7 non-afflicted MM patients. In addition, MM patients who achieved good responses to nivolumab significantly exhibited decreased serum TNF-α levels after nivolumab treatment compared to progressive MM patients.

摘要

纳武单抗是一种用于恶性黑色素瘤(MM)患者的标准重组抗体治疗药物,它通过阻断T细胞中的程序性细胞死亡-1(PD-1)途径发挥免疫检查点抑制剂的作用。然而,它会导致各种免疫相关不良事件(irAE),并且还会加重潜在的自身免疫性疾病。在此我们报告MM合并irAE的病例。病例1:一名69岁的MM女性在接受3剂纳武单抗治疗后发生破坏性甲状腺炎,导致甲状腺功能减退,并接受了甲状腺辅助治疗。病例2:一名80岁的MM男性在接受4剂纳武单抗治疗后急性发作甲状腺功能亢进。病例3:一名85岁的MM女性在接受2剂纳武单抗治疗后发生多神经根神经病,导致躯体感觉障碍和肌肉无力,并接受了静脉注射免疫球蛋白和口服泼尼松龙(40毫克/天)治疗。病例4:一名77岁的MM男性在局部注射干扰素-β和接受11剂纳武单抗治疗后发生银屑病样皮炎。病例5:病例2也发生了银屑病样皮炎。我们分析了MM患者在接受纳武单抗治疗前后血清炎症细胞因子水平。所有6例在接受纳武单抗治疗后发生有或无银屑病病史的银屑病样皮炎的患者,以及所有7例发生其他irAE的患者在纳武单抗治疗后血清IL-6水平均升高,而7例未受累的MM患者中有5例血清IL-6水平降低。此外,与疾病进展的MM患者相比,对纳武单抗治疗反应良好的MM患者在纳武单抗治疗后血清TNF-α水平显著降低。

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