Lankes Katharina, Hundorfean Gheorghe, Harrer Thomas, Pommer Ansgar J, Agaimy Abbas, Angelovska Irena, Tajmir-Riahi Azadeh, Göhl Jonas, Schuler Gerold, Neurath Markus F, Hohenberger Werner, Heinzerling Lucie
Department of Dermatology, University Hospital Erlangen , Ulmenweg 18 , Erlangen, Germany.
Department of Gastroenterology, Pneumology and Endocrinology, University Hospital Erlangen , Ulmenweg 18 , Erlangen, Germany.
Oncoimmunology. 2016 Feb 18;5(6):e1128611. doi: 10.1080/2162402X.2015.1128611. eCollection 2016 Jun.
Immune-related adverse events (irAEs) induced by checkpoint inhibitors are well known. Since fatal outcomes have been reported early detection and adequate management are crucial. In particular, colitis is frequently observed and can result in intestinal perforation. This is the first report of an autoimmune colitis that was treated according to algorithms but became resistant due to a CMV reactivation. The 32-y-old male patient with metastatic melanoma treated within an anti-PD-1/ipilimumab combination study developed severe immune-mediated colitis (CTCAE grade 3) with up to 18 watery stools per day starting 2 weeks after treatment initiation. After improving upon therapy with immunosuppressive treatment (high dose steroids and infliximab) combined with parenteral nutrition diarrhea again exacerbated. Additionally, the patient had asymptomatic grade 3 CTCAE amylase and lipase elevation. Colitis was monitored by weekly endoscopies and colon biopsies were analyzed histologically with CMV staining, multi-epitope ligand cartography (MELC) and qRT-PCR for inflammatory genes. In the course, CMV reactivation was detected in the colon and treated with antiviral medication in parallel to a reduction of corticosteroids. Subsequently, symptoms improved. The patient showed a complete response for 2 y now including regression of bone metastases. CMV reactivation under checkpoint inhibitor therapy in combination with immunosuppressive treatment for autoimmune side effects has to be considered in these patients and if present treated. Potentially, CMV reactivation is underdiagnosed. Treatment algorithms should include CMV diagnostics.
由检查点抑制剂引起的免疫相关不良事件(irAEs)已广为人知。由于已有致命后果的报道,早期检测和适当管理至关重要。特别是,结肠炎经常被观察到,并且可能导致肠穿孔。这是第一例根据算法治疗但因巨细胞病毒(CMV)重新激活而产生耐药性的自身免疫性结肠炎报告。一名32岁的转移性黑色素瘤男性患者在一项抗PD-1/伊匹单抗联合研究中接受治疗,在开始治疗2周后出现严重的免疫介导性结肠炎(CTCAE 3级),每天多达18次水样便。在接受免疫抑制治疗(高剂量类固醇和英夫利昔单抗)联合肠外营养治疗后病情改善,但腹泻再次加剧。此外,患者出现无症状的CTCAE 3级淀粉酶和脂肪酶升高。通过每周进行内镜检查监测结肠炎,并对结肠活检组织进行组织学分析,采用CMV染色、多表位配体图谱分析(MELC)和炎症基因定量逆转录聚合酶链反应(qRT-PCR)。在此过程中,在结肠中检测到CMV重新激活,并在减少皮质类固醇的同时给予抗病毒药物治疗。随后,症状有所改善。该患者目前已完全缓解2年,包括骨转移灶消退。在这些接受检查点抑制剂治疗并联合免疫抑制治疗自身免疫副作用的患者中,必须考虑CMV重新激活的情况,如有发生应进行治疗。CMV重新激活可能存在诊断不足的情况。治疗算法应包括CMV诊断。