Department of Respiratory Medicine, Shonan Fujisawa Tokushukai Hospital, Kanagawa, Japan.
Department of Respiratory Medicine, Yao Tokushukai General Hospital, Osaka, Japan.
J Thorac Oncol. 2022 Aug;17(8):1002-1013. doi: 10.1016/j.jtho.2022.05.015. Epub 2022 Jun 22.
Patients with cancer have been prioritized for vaccination against severe acute respiratory syndrome coronavirus 2. Nevertheless, there are limited data regarding the safety, efficacy, and risk of developing immune-related adverse events (irAEs) associated with mRNA vaccines in patients with lung cancer, especially those being actively treated with immune checkpoint inhibitors.
This multicenter observational study was conducted at nine hospitals in Japan. Patients with lung cancer (≥20 y) actively treated with immune checkpoint inhibitors between 4 weeks prefirst vaccination and 4 weeks postsecond vaccination were enrolled. The primary end point was the incidence of irAEs of any grade on the basis of an assumed incidence without vaccination rate of 35%. Immunogenicity was assessed by measuring anti-spike (S)-IgG antibody levels against severe acute respiratory syndrome coronavirus 2.
A total of 126 patients with lung cancer (median age, 71 y; interquartile range, 65-74) were enrolled from May to November 2021 and followed up until December 2021. There were 26 patients (20.6%, 95% confidence interval: 13.9%-28.8%) and seven patients (5.6%, 95% confidence interval: 2.3%-11.1%) who developed irAEs of any grade pre- and postvaccination, respectively, which was lower than the predicted incidence without vaccination. None of the patients experienced exacerbation of preexisting irAE postvaccination. S-IgG antibodies were seroconverted in 96.7% and 100% of the patients with lung cancer and controls, respectively, but antibody levels were significantly lower in patients with lung cancer (p < 0.001).
Patients with lung cancer who were actively treated with ICIs were safely vaccinated without an increased incidence of irAEs; however, their vaccine immunogenicity was lower. This requires further evaluation.
患有癌症的患者已被优先接种针对严重急性呼吸综合征冠状病毒 2 的疫苗。然而,关于肺癌患者接种 mRNA 疫苗的安全性、有效性和免疫相关不良事件(irAE)风险的数据有限,尤其是那些正在接受免疫检查点抑制剂积极治疗的患者。
本多中心观察性研究在日本的 9 家医院进行。招募了在首次接种前 4 周至第二次接种后 4 周内正在接受免疫检查点抑制剂积极治疗的肺癌(≥20 岁)患者。主要终点是根据无疫苗接种率为 35%的假设发生率,任何等级 irAE 的发生率。通过测量针对严重急性呼吸综合征冠状病毒 2 的抗刺突(S)-IgG 抗体水平来评估免疫原性。
2021 年 5 月至 11 月期间共招募了 126 名肺癌患者(中位年龄 71 岁;四分位间距 65-74),并随访至 2021 年 12 月。分别有 26 名(20.6%,95%置信区间:13.9%-28.8%)和 7 名(5.6%,95%置信区间:2.3%-11.1%)患者在接种前和接种后分别出现任何等级的 irAE,这低于无疫苗接种的预测发生率。无一例患者在接种后出现先前存在的 irAE 恶化。肺癌患者和对照组的 S-IgG 抗体均分别有 96.7%和 100%发生血清转化,但肺癌患者的抗体水平明显较低(p<0.001)。
正在接受 ICIs 积极治疗的肺癌患者接种疫苗是安全的,不会增加 irAE 的发生率;然而,他们的疫苗免疫原性较低。这需要进一步评估。