Department of Hospital Medicine, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 1465, Houston, TX, 77030, USA.
Division of Oncology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Support Care Cancer. 2024 Feb 16;32(3):160. doi: 10.1007/s00520-024-08361-1.
Immune checkpoint inhibitors (ICI) have become standard of care for some types of lung cancer. Along with expanding usage comes the emergence of immune-related adverse events (irAEs), including ICI-related pneumonitis (ICI-P). Treatment guidelines for managing irAEs have been developed; however, how clinicians manage irAEs in the real-world setting is less well known. We aimed to describe the outcomes and care patterns of grade ≥ 3 ICI-P in an onco-hospitalist service.
We included patients with lung cancer treated with ICI who were admitted to an oncology hospitalist service with a suspicion of ICI-P. We described the hospitalization characteristics, treatment patterns, discharge practices, and clinical outcomes of patients with confirmed ICI-P. The primary outcome was time to start treatment for ICI-P.
Among 49 patients admitted with a suspicion of ICI-P, 31 patients were confirmed to have ICI-P and subsequently received ICI-P directed treatment. Pulmonology was consulted in 97% of patients. Median time to start treatment for ICI-P was 1 day (IQR 0-3.5 days). All 31 patients received corticosteroids. Inpatient mortality was 32%. Majority of patients discharged with steroids were prescribed prophylaxis for gastritis and opportunistic infections. Thirty-eight percent of patients were seen by pulmonology and 86% were seen by the oncology team post-discharge.
Our study confirms prior findings of high mortality among patients with high-grade ICI-P. Early diagnosis and treatment are key to improving clinical outcomes. Understanding the care patterns and adherence to treatment guidelines of clinicians caring for this patient population may help identify ways to further standardize management practices and improve patient outcomes.
免疫检查点抑制剂(ICI)已成为某些类型肺癌的标准治疗方法。随着使用范围的扩大,出现了免疫相关不良事件(irAE),包括 ICI 相关性肺炎(ICI-P)。已经制定了管理 irAE 的治疗指南;然而,临床医生在实际环境中如何管理 irAE 知之甚少。我们旨在描述肿瘤科医生服务中≥3 级 ICI-P 的结局和护理模式。
我们纳入了接受 ICI 治疗的肺癌患者,这些患者因疑似 ICI-P 而被收入肿瘤科医生服务。我们描述了确诊为 ICI-P 的患者的住院特征、治疗模式、出院实践和临床结局。主要结局是开始治疗 ICI-P 的时间。
在因疑似 ICI-P 而住院的 49 名患者中,有 31 名患者被确诊为 ICI-P,并随后接受了 ICI-P 定向治疗。97%的患者咨询了肺病科。开始治疗 ICI-P 的中位时间为 1 天(IQR 0-3.5 天)。所有 31 名患者均接受了皮质类固醇治疗。31 名患者中有 32%住院期间死亡。大多数带皮质类固醇出院的患者都被开了预防胃炎和机会性感染的药物。38%的患者接受了肺病科的治疗,86%的患者在出院后接受了肿瘤科团队的治疗。
我们的研究证实了先前关于高等级 ICI-P 患者死亡率高的发现。早期诊断和治疗是改善临床结局的关键。了解照顾这一患者群体的临床医生的护理模式和对治疗指南的遵循情况,可能有助于找到进一步规范管理实践和改善患者结局的方法。