Cameli Paolo, Faverio Paola, Ferrari Katia, Bonti Viola, Marsili Stefania, Mazzei Maria Antonietta, Mazzoni Francesca, Bartolucci Maurizio, Scotti Vieri, Bertolini Federica, Barbieri Fausto, Baldessari Cinzia, Veronese Chiara, Boffi Roberto, Brighenti Matteo, Cortinovis Diego, Dominici Massimo, Pesci Alberto, Bargagli Elena, Luppi Fabrizio
Respiratory Diseases Unit, Department of Medicine, Surgery and Neurosciences, Siena University Hospital, University of Siena, 53100 Siena, Italy.
Respiratory Unit, University of Milan-Bicocca, S. Gerardo Hospital, 20900 Monza, Italy.
Life (Basel). 2022 Jul 29;12(8):1149. doi: 10.3390/life12081149.
Immune checkpoint inhibitors (ICIs) have revolutionized the therapeutic horizons of various cancers. However, immune-related adverse events have been reported, including interstitial lung diseases. Our aim was to describe the clinical and radiological features and survival of a multicentre cohort of patients who developed ICI-related lung toxicity.
Six Italian centres were involved in the study. Patients who were treated with anti-PD-1/PD-L1 and CTLA-4 mAbs and developed ICI-related lung toxicity were recruited retrospectively to study clinical, radiological, immunological and survival data.
A total of 41 patients (25 males, 66.8 ± 9.9 years) were enrolled. Lung toxicity occurred after 204.3 ± 208.3 days of therapy, with ground glass opacities being the most common HRCT pattern (23 cases). Male sex, lung cancer and acute respiratory failure were associated with a shorter latency of toxicity ( = 0.0030, = 0.0245 and = 0.0390, respectively). Patients who required high-flow oxygen therapy showed significantly worse survival ( = 0.0028).
Our cohort showed heterogeneous clinical and radiological aspects of ICI-related lung toxicity, with a latency not limited to the first year of treatment. Severity was mainly mild to moderate, although life-threatening events did occur. Our data indicate that strict long-term follow-up is needed to enable early diagnosis and appropriate management.
免疫检查点抑制剂(ICIs)彻底改变了各种癌症的治疗前景。然而,已报告了免疫相关不良事件,包括间质性肺疾病。我们的目的是描述发生ICI相关肺部毒性的多中心队列患者的临床、放射学特征及生存情况。
六个意大利中心参与了该研究。回顾性招募接受抗PD-1/PD-L1和CTLA-4单克隆抗体治疗并发生ICI相关肺部毒性的患者,以研究临床、放射学、免疫学和生存数据。
共纳入41例患者(25例男性,年龄66.8±9.9岁)。肺部毒性在治疗204.3±208.3天后出现,磨玻璃影是最常见的高分辨率CT表现(23例)。男性、肺癌和急性呼吸衰竭与毒性潜伏期较短相关(分别为P = 0.0030、P = 0.0245和P = 0.0390)。需要高流量氧疗的患者生存情况明显更差(P = 0.0028)。
我们的队列显示了ICI相关肺部毒性的临床和放射学特征具有异质性,潜伏期不限于治疗的第一年。严重程度主要为轻度至中度,尽管确实发生了危及生命的事件。我们的数据表明需要进行严格的长期随访以实现早期诊断和适当管理。