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免疫检查点抑制剂相关肺炎:一项叙述性综述。

Immune Checkpoint Inhibitor-associated Pneumonitis: A Narrative Review.

作者信息

Li Chang, Faiz Saadia A, Boysen-Osborn Megan, Sheshadri Ajay, Wattana Monica K

机构信息

McGovern Medical School at University of Texas Health, Divisions of Pulmonary, Critical Care Medicine and Sleep Medicine, Houston, Texas.

The University of Texas MD Anderson Cancer Center, Department of Pulmonary Medicine, Houston, Texas.

出版信息

West J Emerg Med. 2025 Mar;26(2):210-218. doi: 10.5811/westjem.20305.

Abstract

Immune checkpoint inhibitors (ICI), such as pembrolizumab, nivolumab, durvalumab and ipilimumab, have significantly enhanced survival rates for multiple cancer types such as non-small cell lung cancer, melanoma, Hodgkin lymphoma, and breast cancer, and they have emerged as an adjunct or primary therapy for malignant disease. Approximately 40% of patients with cancer on ICI therapy experience side effects called immune-related adverse events (irAE). While not the most common, pulmonary toxicities can be rapidly progressive, potentially fatal, and pose a three-fold increased risk for requiring intensive care unit-level of care. Pneumonitis is a focal or diffuse inflammation of the lung parenchyma, and clinical manifestations may be highly variable. While the onset is generally observed 6-12 weeks after the initiation of therapy, drug toxicity can develop rapidly within days after the first infusion or many months into therapy. Pneumonitis symptoms can be subtle or non-specific; therefore, a thorough and systematic evaluation considering other possible etiologies is crucial. Moreover, extrapulmonary findings, such as skin lesions, colitis, or endocrinopathies, should raise suspicion for irAE as drug toxicity can affect multiple organs simultaneously. Due to the significant overlap of clinical features between ICI-associated pneumonitis and respiratory infections, it can be challenging to differentiate the two conditions based on clinical presentation alone. A multidisciplinary approach to management is recommended for the treatment of ICI-associated pneumonitis, and classification of severity helps to guide interventions. Treatment options in more severe cases include systemic immunosuppression. Given the increased use of ICIs and greater probability that patients with ICI-associated pneumonitis will be seen in the emergency department, we aimed to provide a comprehensive framework for the diagnosis and management. In addition, identifying potential challenges in diagnosis and/or other contributors of respiratory symptoms and radiographic manifestations is highlighted.

摘要

免疫检查点抑制剂(ICI),如帕博利珠单抗、纳武利尤单抗、度伐利尤单抗和伊匹木单抗,显著提高了多种癌症类型(如非小细胞肺癌、黑色素瘤、霍奇金淋巴瘤和乳腺癌)的生存率,并且已成为恶性疾病的辅助或主要治疗方法。接受ICI治疗的癌症患者中约40%会出现称为免疫相关不良事件(irAE)的副作用。肺部毒性虽然不是最常见的,但可能迅速进展,有潜在致命风险,且需要重症监护病房级护理的风险增加了两倍。肺炎是肺实质的局灶性或弥漫性炎症,临床表现可能差异很大。虽然一般在治疗开始后6至12周出现,但药物毒性可在首次输注后数天内迅速发展,或在治疗数月后出现。肺炎症状可能很轻微或不具特异性;因此,全面系统地评估其他可能病因至关重要。此外,肺外表现,如皮肤病变、结肠炎或内分泌病,应引起对irAE的怀疑,因为药物毒性可同时影响多个器官。由于ICI相关肺炎和呼吸道感染的临床特征有很大重叠,仅根据临床表现区分这两种情况可能具有挑战性。建议采用多学科方法治疗ICI相关肺炎,严重程度分类有助于指导干预措施。更严重病例的治疗选择包括全身免疫抑制。鉴于ICI使用增加,且急诊科更有可能见到ICI相关肺炎患者,我们旨在提供一个全面的诊断和管理框架。此外,还强调了识别诊断中的潜在挑战和/或呼吸道症状及影像学表现的其他促成因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d49/11931710/ffe1d4375b92/wjem-26-210-g001.jpg

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