Machida Maiko, Yamazaki Chika, Kouda Nao, Hanai Yousei, Sato Hideki, Konda Ainari, Yamagata Yuka, Itho Tatsuya, Aisaka Haruhiko
Department of Pharmacotherapy, Faculty of Pharmaceutical Sciences, Hokkaido University of Science, 7-15-4-1 Maeda Teine, Sapporo, Hokkaido, 006-8585, Japan.
Department of Pharmacy and Respiratory Medicine, Japan Community Health Care Organization Sapporo Hokushin Hospital, 2-6-2-1 Atsubetsu Chou Atsubetsu, Sapporo, Hokkaido, 004-8618, Japan.
J Pharm Health Care Sci. 2022 Dec 5;8(1):29. doi: 10.1186/s40780-022-00261-y.
Immunotherapy with immune checkpoint inhibitors is associated with immune-related adverse events (irAEs). A positive correlation between treatment efficacy and irAEs has been reported. Clinical indicators are required for appropriate interventions, such as steroid administration, to prevent fatal outcomes. Nuclear receptor transcription factor 4a (Nr4a), which is involved in T-cell anergy, exhaustion, and regulatory T cells, were observed not only in thymocytes but in peripheral blood mononuclear cells. We describe a case of Stevens-Johnson syndrome (SJS) that was induced by a single dose of pembrolizumab and successfully treated with steroids, leading to complete remission of lung cancer during the monitoring of immune response indices, including Nr4a1 mRNA.
A 68-year-old male with squamous cell lung cancer (cT2aN3M0, stage IIIb) received a single dose of pembrolizumab (200 mg). On Day 21 of treatment, SJS appeared, and the patient was treated with prednisolone 60 mg/day, which was gradually tapered off. After the disappearance of the SJS symptoms, complete remission of cancer was achieved and was maintained for more than 1 year. Acute increases in the plasma IFN-γ and IL-17 concentrations and a decrease in IL-10 concentrations were observed at the onset of SJS. Simple regression analysis showed that these changes in IL-17, IFN-γ and IL-10 were significantly influenced by the decreased expression of Nr4a1 mRNA. The pembrolizumab levels and prednisolone doses significantly influenced the suppression of Nr4a1 mRNA levels. Although Nr4a1 mRNA levels in the current case fluctuated during the observation period, they were significantly lower than those in a nonresponding progressive-disease case, as well as a pembrolizumab-responding case with non-SJS but similar background. The suppression of Nr4a1 in current case, might result in upregulation of cytotoxic T cells and a reduction in functional regulatory T cells, promoting favorable antitumor immunity.
The immune responses involving Nr4a1 suppression might relate to complete remission of lung cancer in this case, despite causing SJS, which may be attributed to synergistic effects from pembrolizumab treatment and intervention with steroids. The current case indicates the preliminarily clinical benefit of evaluating Nr4a expression-related indices as the possible clinical covariates and may serve as a milestone for appropriate future chemotherapy interventions.
免疫检查点抑制剂免疫疗法与免疫相关不良事件(irAE)相关。已有报道称治疗疗效与irAE之间存在正相关。需要临床指标来进行适当干预,如使用类固醇,以防止出现致命后果。核受体转录因子4a(Nr4a)参与T细胞无反应性、耗竭及调节性T细胞的形成,不仅在胸腺细胞中可观察到,在外周血单个核细胞中也可观察到。我们报告一例由单剂量派姆单抗诱发的史蒂文斯-约翰逊综合征(SJS)病例,该病例经类固醇成功治疗,在监测包括Nr4a1 mRNA在内的免疫反应指标期间肺癌完全缓解。
一名68岁的男性鳞状细胞肺癌患者(cT2aN3M0,Ⅲb期)接受了单剂量派姆单抗(200 mg)治疗。在治疗第21天,出现了SJS,患者接受泼尼松龙60 mg/天治疗,剂量逐渐减少。SJS症状消失后,癌症实现完全缓解,并维持了1年多。在SJS发病时观察到血浆IFN-γ和IL-17浓度急性升高,IL-10浓度降低。简单回归分析表明,IL-17、IFN-γ和IL-10的这些变化受Nr4a1 mRNA表达降低的显著影响。派姆单抗水平和泼尼松龙剂量对Nr4a1 mRNA水平的抑制有显著影响。虽然本例中Nr4a1 mRNA水平在观察期内有波动,但显著低于无反应的疾病进展病例以及背景相似但无SJS的派姆单抗反应性病例。本例中Nr4a1的抑制可能导致细胞毒性T细胞上调及功能性调节性T细胞减少,从而促进有利的抗肿瘤免疫。
尽管导致了SJS,但涉及Nr4a1抑制的免疫反应可能与该病例中肺癌的完全缓解有关,这可能归因于派姆单抗治疗和类固醇干预的协同作用。本例表明,将Nr4a表达相关指标作为可能的临床协变量进行评估具有初步临床益处,可能为未来适当的化疗干预提供一个里程碑。