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免疫检查点抑制剂诱发肺炎患者的长期预后

Long-term outcomes in patients with immune checkpoint inhibitor induced pneumonitis.

作者信息

Davis Andrea, Johnson Douglas B, Bastarache Julie A

机构信息

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA

Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

出版信息

BMJ Open Respir Res. 2023 Apr 6;10(1):e001342. doi: 10.1136/bmjresp-2022-001342.

Abstract

INTRODUCTION

Immune checkpoint inhibitors (ICI) have improved outcomes for patients with many malignancies. However, these treatments are associated with immune-related adverse events, including pulmonary toxicity (pneumonitis). Pneumonitis is associated with significant short-term morbidity and mortality, but long-term outcomes are not well described.

METHODS

We used the Vanderbilt Synthetic Derivative, a deidentified electronic health record database of >2.5 million patients seen at Vanderbilt, to identify patient charts that included treatment with pembrolizumab, nivolumab, ipilimumab, ipilimumab and nivolumab, atezolizumab or durvalumab by keyword search and ICD-10 codes for acute respiratory failure and/or bronchoalveolar lavage. We manually reviewed these charts and identified 78 subjects who met criteria for probable pneumonitis which included patients presenting with symptoms (dyspnoea, hypoxia, cough) and/or CT imaging consistent with this diagnosis. We collected data on demographics, ICI regimen, hospital admissions and long-term survival.

RESULTS

Of the 78 patients (48 males; median age 64 (range 28-81)), 52 patients required at least 1 hospital admission related to pneumonitis. A total of 25 patients experienced poor short-term outcomes (including 6 referred to hospice, 11 discharged to rehabilitation and 9 deaths). There was no association with these outcomes by patient age (p=0.96), sex (p=0.60), smoking status (p=0.63) or cancer type (p=0.13). Median duration of follow-up was 8.3 months (range 0.2-110.6 months), and 29 patients (37%) were alive at last follow-up. Patients admitted to the hospital were more likely to die (p=0.002) and less likely to receive additional treatment (p<0.0001) or survive for ≥12 months with no evidence of disease (p=0.02). There were no differences in long-term outcomes for patients with underlying pulmonary comorbidities.

DISCUSSION

ICI-pneumonitis has a high likelihood of causing hospitalisation and poor outcomes, including death. While there appears to be no difference in outcomes for patients with underling pulmonary comorbidities, those requiring admission have worse outcomes.

摘要

引言

免疫检查点抑制剂(ICI)改善了许多恶性肿瘤患者的治疗效果。然而,这些治疗与免疫相关不良事件有关,包括肺部毒性(肺炎)。肺炎与显著的短期发病率和死亡率相关,但长期预后尚无充分描述。

方法

我们使用范德比尔特合成衍生物,这是一个对范德比尔特超过250万患者进行去识别处理的电子健康记录数据库,通过关键词搜索以及急性呼吸衰竭和/或支气管肺泡灌洗的ICD-10编码来识别包含派姆单抗、纳武单抗、伊匹单抗、伊匹单抗和纳武单抗、阿特珠单抗或度伐鲁单抗治疗的患者病历。我们人工查阅这些病历,确定了78名符合可能肺炎标准的受试者,这些患者出现了症状(呼吸困难、低氧、咳嗽)和/或CT影像与该诊断相符。我们收集了人口统计学、ICI治疗方案、住院情况和长期生存的数据。

结果

78例患者(48例男性;中位年龄64岁(范围28 - 81岁))中,52例患者因肺炎至少需要1次住院治疗。共有25例患者短期预后较差(包括6例转入临终关怀、11例出院接受康复治疗和9例死亡)。这些预后与患者年龄(p = 0.96)、性别(p = 0.60)、吸烟状况(p = 0.63)或癌症类型(p = 0.13)无关。中位随访时间为8.3个月(范围0.2 - 110.6个月),末次随访时29例患者(37%)存活。住院患者死亡可能性更大(p = 0.002),接受额外治疗的可能性更小(p < 0.0001),或无疾病证据存活≥12个月的可能性更小(p = 0.02)。有潜在肺部合并症的患者长期预后无差异。

讨论

ICI相关性肺炎很可能导致住院和不良预后,包括死亡。虽然有潜在肺部合并症的患者预后似乎无差异,但需要住院治疗的患者预后更差。

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本文引用的文献

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Immune Checkpoint Inhibitor-Related Pneumonitis.免疫检查点抑制剂相关性肺炎。
Respiration. 2020;99(11):932-942. doi: 10.1159/000509941. Epub 2020 Dec 1.

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