Aiad Mina, Fresco Kayla, Prenatt Zarian, Tahir Ali, Ramos-Feliciano Karla, Stoltzfus Jill, Harmouch Farah, Wilson Melissa
Internal Medicine, St. Luke's University Health Network, Bethlehem, USA.
Internal Medicine, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
Cureus. 2022 Jun 5;14(6):e25665. doi: 10.7759/cureus.25665. eCollection 2022 Jun.
Introduction Radiation pneumonitis (RP) is a common dose-limiting toxicity of radiotherapy to the chest in lung cancer patients. Similarly, the revolutionary use of immune checkpoint inhibitors (ICIs) to treat lung cancer can be complicated by immune-related adverse events (irAEs), particularly checkpoint inhibitor pneumonitis (CIP). Our study aimed to assess the effect of immunotherapy, with and without radiotherapy, on pneumonitis and other outcomes. Methods We performed a retrospective chart review of 680 lung cancer patients treated with either radiotherapy, immunotherapy, or both at St. Luke's University Health Network to determine the incidence rates of pneumonitis. Then, a more extensive review of 346 patients was completed, 181 of whom had pneumonitis, to investigate risk factors and outcomes. Results All-grade pneumonitis incidence was 26.6% while more severe pneumonitis (grade 3 or higher) was 13%. Receiving programmed cell death-1 (PD-1) or ligand-1 (PD-L1) inhibitors, having squamous cell carcinoma (SCC), and having poorer performance status were independently and significantly associated with increased risk of pneumonitis, with AOR (adjusted odds ratios) of 8.32, 4.10, 2.91, and 1.71, respectively. Among those who had pneumonitis, more severe cases (grade 3 or higher) were related to immunotherapy, either alone (58.32%) or with radiation (55.7%), compared to radiation therapy alone (36.2%). Poorer performance status (defined as a higher Eastern Cooperative Oncology Group (ECOG) score) was the only covariate we found to be significantly and independently associated with reduced odds of 18-months survival. More of the patients treated with both lung radiation and immunotherapy had progressive disease (53.8%) compared to those treated with only radiation (30.4%) or immunotherapy (36.7). Progressive disease occurred more in patients with pneumonitis grade 3 or higher (48.3%) than those with no or low-grade pneumonitis (27.2%). Conclusion Receiving PD-L1 and PD-1 inhibitors, either with or without radiotherapy, was associated with a higher risk of more severe pneumonitis (PD-L1 > PD-1) than radiotherapy alone. Given its high incidence and complications, more about therapy-induced pneumonitis is yet to be studied. Learning more about pneumonitis' risk factors and complications is of great clinical importance, as it may result in better treatment planning and improved outcomes. Future studies are needed to investigate the suggested association between symptomatic pneumonitis and poorer response to treatment and whether SCC increases the risk of higher-grade pneumonitis.
引言
放射性肺炎(RP)是肺癌患者胸部放疗常见的剂量限制性毒性反应。同样,免疫检查点抑制剂(ICI)用于治疗肺癌的创新性应用可能会并发免疫相关不良事件(irAE),尤其是检查点抑制剂肺炎(CIP)。我们的研究旨在评估免疫治疗联合或不联合放疗对肺炎及其他结局的影响。
方法
我们对圣卢克大学健康网络中接受放疗、免疫治疗或两者联合治疗的680例肺癌患者进行了回顾性病历审查,以确定肺炎的发病率。然后,对346例患者进行了更广泛的审查,其中181例患有肺炎,以调查危险因素和结局。
结果
所有级别的肺炎发病率为26.6%,而更严重的肺炎(3级或更高)为13%。接受程序性细胞死亡蛋白1(PD-1)或配体1(PD-L1)抑制剂、患有鳞状细胞癌(SCC)以及身体状况较差与肺炎风险增加独立且显著相关,调整后的比值比(AOR)分别为8.32、4.10、2.91和1.71。在患有肺炎的患者中,更严重的病例(3级或更高)与免疫治疗相关,单独免疫治疗(58.32%)或联合放疗(55.7%),相比单纯放疗(36.2%)。身体状况较差(定义为东部肿瘤协作组(ECOG)评分较高)是我们发现的唯一与18个月生存率降低显著且独立相关的协变量。与仅接受放疗(30.4%)或免疫治疗(36.7%)的患者相比,接受肺部放疗和免疫治疗联合治疗的患者更多出现疾病进展(53.8%)。3级或更高级别肺炎患者的疾病进展发生率(48.3%)高于无肺炎或低级别肺炎患者(27.2%)。
结论
接受PD-L1和PD-1抑制剂,无论是否联合放疗,与比单纯放疗更高的更严重肺炎风险相关(PD-L1>PD-1)。鉴于其高发病率和并发症,关于治疗引起的肺炎仍有更多需要研究。了解更多肺炎的危险因素和并发症具有重要的临床意义,因为这可能导致更好的治疗计划和改善结局。未来需要研究有症状肺炎与治疗反应较差之间的潜在关联,以及SCC是否会增加更高级别肺炎的风险。