Department of Internal Medicine, Division of Medical Oncology, University of Colorado Cancer Center, University of Anschutz Medical Campus, Aurora, CO, USA.
Department of Biostatistics, University of Colorado Cancer Center Biostatistics Core, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Hum Vaccin Immunother. 2023 Dec 31;19(1):2207438. doi: 10.1080/21645515.2023.2207438. Epub 2023 May 9.
The incidence of severe immune-related adverse events (irAEs) in cancer subjects receiving immune checkpoint inhibitors (ICIs) following COVID-19 vaccination and the relationship between the incidence of severe irAE and the interval between COVID-19 vaccination and ICI dose have not been established. We performed a retrospective study evaluating the incidence of irAEs in solid tumor subjects receiving ICI therapy who received any COVID-19 vaccinations since FDA authorization. irAEs were defined as severe with one or more grade 3 or above events (CTCAE v5.0), multiple organ involvement, or requiring hospitalization for management. Two hundred and eighty-four subjects who received COVID vaccinations from December 2020 and February 2022 were included in this analysis [median age at vaccination 67 years (IQR 59.0-75.0); 67.3% male]. Twenty-nine subjects (10.2%) developed severe irAEs, of which 12 subjects (41.4%) received ICI monotherapy, 10 subjects (34.5%) received combination ICI therapy with nivolumab and ipilimumab, and 7 subjects (24.1%) received ICI plus VEGFR-TKI therapy. Hospitalization occurred in 62% of subjects with severe irAEs, with a median duration of 3 days (IQR: 3.0-7.5 days). Immunosuppressive therapy was required in 79.3%, with a median duration of 103 days (IQR: 42.0-179.0). ICI therapy was discontinued in 51.7% of subjects with severe irAE; dosing was held or interrupted in 34.5%. Among severe irAEs, the median interval between vaccination and ICI treatment closest to the occurrence of severe irAE was 15.5 days (IQR: 10.0-23.0). In solid tumor cancer subjects receiving ICIs, COVID-19 vaccination is not associated with an increased incidence of severe irAEs compared to historical data and may be safely administered during ICI cancer therapy in subjects who lack contraindications.
在接受 COVID-19 疫苗接种后接受免疫检查点抑制剂(ICI)治疗的癌症患者中,严重免疫相关不良事件(irAE)的发生率以及严重 irAE 的发生率与 COVID-19 疫苗接种和 ICI 剂量之间的间隔之间的关系尚未确定。我们进行了一项回顾性研究,评估了自 FDA 批准以来接受 ICI 治疗的实体瘤患者在接受任何 COVID-19 疫苗接种后的 irAE 发生率。irAE 被定义为具有一个或多个 3 级或以上事件(CTCAE v5.0)、多器官受累或需要住院治疗的严重 irAE。本分析纳入了 284 名在 2020 年 12 月至 2022 年 2 月期间接种 COVID 疫苗的患者[接种疫苗时的中位年龄为 67 岁(IQR 59.0-75.0);67.3%为男性]。29 名患者(10.2%)发生严重 irAE,其中 12 名患者(41.4%)接受 ICI 单药治疗,10 名患者(34.5%)接受纳武利尤单抗和伊匹单抗联合 ICI 治疗,7 名患者(24.1%)接受 ICI 联合 VEGFR-TKI 治疗。发生严重 irAE 的患者中有 62%需要住院治疗,中位持续时间为 3 天(IQR:3.0-7.5 天)。79.3%需要免疫抑制治疗,中位持续时间为 103 天(IQR:42.0-179.0)。51.7%发生严重 irAE 的患者停止了 ICI 治疗;34.5%的患者暂停或中断了 ICI 治疗。在严重 irAE 中,接种疫苗和 ICI 治疗之间最接近发生严重 irAE 的中位间隔为 15.5 天(IQR:10.0-23.0)。在接受 ICI 治疗的实体瘤癌症患者中,与历史数据相比,COVID-19 疫苗接种并不会增加严重 irAE 的发生率,并且在缺乏禁忌症的情况下,在接受 ICI 癌症治疗期间可安全接种。