Hospital for Special Surgery Division of Rheumatology, New York, New York, USA
Weill Cornell Medicine, New York, New York, USA.
J Immunother Cancer. 2020 Oct;8(2). doi: 10.1136/jitc-2020-001550.
Immune checkpoint inhibitors (ICI) block negative regulatory molecules, such as CTLA-4, PD-1 and PD-L1, in order to mount an antitumor response. T cells are important for antiviral defense, but it is not known whether patients with cancer treated with ICI are more or less vulnerable to viral infections such as COVID-19. Furthermore, immunosuppressive treatment of immune-related adverse events (irAE) may also impact infection risk. Rheumatic irAEs are often persistent, and can require long-term treatment with immunosuppressive agents. The aim of this study was to determine the incidence of COVID-19 infection and assess changes in ICI and immunosuppressive medication use among patients enrolled in a prospective rheumatic irAE registry during the height of the COVID-19 pandemic. On April 16 2020, following the 'surge' of COVID-19 infections in the New York Tri-State area, we sent a 23-question survey to 88 living patients enrolled in a single institutional registry of patients with rheumatic irAE. Questions addressed current cancer and rheumatic irAE status, ICI and immunosuppressant medication use, history of COVID-19 symptoms and/or diagnosed infection. A follow-up survey was sent out 6 weeks later. Sixty-five (74%) patients completed the survey. Mean age was 63 years, 59% were female, 70% had received anti-PD-(L)1 monotherapy and 80% had had an irAE affecting their joints. Six patients (10%) had definite or probable COVID-19, but all recovered uneventfully, including two still on ICI and on low-to-moderate dose prednisone. Of the 25 on ICI within the last 6 months, seven (28%) had their ICI held due to the pandemic. In patients on immunosuppression for irAE, none had changes made to those medications as a result of the pandemic. The incidence of COVID-19 was no higher in patients still on ICI. Ten percent of rheumatic irAE patients developed COVID-19 during the NY Tri-state 'surge' of March-April 2020. Oncologists held ICI in a quarter of the patients still on them, particularly women, those on anti-PD-(L)1 monotherapy, and those who had had a good cancer response. The incidence of COVID-19 was no higher on patients still on ICI. None of the patients on disease-modifying antirheumatic drugs or biological immunosuppressive medications developed COVID-19.
免疫检查点抑制剂 (ICI) 阻断负性调节分子,如 CTLA-4、PD-1 和 PD-L1,以引发抗肿瘤反应。T 细胞对于抗病毒防御很重要,但尚不清楚接受 ICI 治疗的癌症患者是否更容易或更不容易感染 COVID-19 等病毒感染。此外,免疫相关不良事件 (irAE) 的免疫抑制治疗也可能影响感染风险。风湿性 irAE 通常是持续性的,并且可能需要长期使用免疫抑制剂进行治疗。本研究旨在确定 COVID-19 感染的发生率,并评估在 COVID-19 大流行高峰期入组前瞻性风湿性 irAE 登记处的患者中 ICI 和免疫抑制药物使用的变化。2020 年 4 月 16 日,在纽约三州地区 COVID-19 感染“激增”之后,我们向入组单一机构风湿性 irAE 患者登记处的 88 名存活患者发送了一份包含 23 个问题的调查问卷。问题涉及当前癌症和风湿性 irAE 状况、ICI 和免疫抑制剂使用情况、COVID-19 症状和/或确诊感染史。6 周后发送了后续调查。65 名患者(74%)完成了调查。平均年龄为 63 岁,59%为女性,70%接受了抗 PD-(L)1 单药治疗,80%的患者 irAE 影响关节。6 名患者(10%)确诊或可能患有 COVID-19,但均顺利康复,包括 2 名仍在接受 ICI 治疗和低至中等剂量泼尼松治疗的患者。在过去 6 个月内接受 ICI 治疗的 25 名患者中,有 7 名(28%)因大流行而暂停 ICI 治疗。在因 irAE 接受免疫抑制治疗的患者中,由于大流行,没有对这些药物进行任何更改。仍在接受 ICI 治疗的患者 COVID-19 发病率并未升高。在 2020 年 3 月至 4 月纽约三州“激增”期间,10%的风湿性 irAE 患者感染了 COVID-19。在仍接受 ICI 治疗的患者中,四分之一的患者暂停了 ICI 治疗,尤其是女性、接受抗 PD-(L)1 单药治疗的患者和癌症反应良好的患者。仍在接受 ICI 治疗的患者 COVID-19 发病率并未升高。未接受疾病修饰抗风湿药物或生物免疫抑制剂治疗的患者未发生 COVID-19。