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本文引用的文献

1
The Clinical Analysis of Checkpoint Inhibitor Pneumonitis with Different Severities in Lung Cancer Patients: A Retrospective Study.肺癌患者不同严重程度的检查点抑制剂肺炎的临床分析:一项回顾性研究
J Clin Med. 2024 Jan 1;13(1):255. doi: 10.3390/jcm13010255.
2
Predictors of immune checkpoint inhibitor-related adverse events in older patients with lung cancer: a prospective real-world analysis.预测肺癌老年患者免疫检查点抑制剂相关不良反应的因素:一项前瞻性真实世界分析。
J Cancer Res Clin Oncol. 2023 Sep;149(11):8993-9006. doi: 10.1007/s00432-023-04792-1. Epub 2023 May 10.
3
Immune checkpoint inhibitor-related pneumonitis in non-small cell lung cancer: A review.非小细胞肺癌中免疫检查点抑制剂相关肺炎:综述
Front Oncol. 2022 Aug 16;12:911906. doi: 10.3389/fonc.2022.911906. eCollection 2022.
4
Immune Checkpoint Inhibitor-Related Pneumonitis in Lung Cancer: Real-World Incidence, Risk Factors, and Management Practices Across Six Health Care Centers in North Carolina.免疫检查点抑制剂相关肺炎在肺癌中的应用:北卡罗来纳州六家医疗中心的真实世界发生率、风险因素和管理实践。
Chest. 2021 Aug;160(2):731-742. doi: 10.1016/j.chest.2021.02.032. Epub 2021 Feb 20.
5
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.
6
Clinical diagnosis and treatment of immune checkpoint inhibitor-associated pneumonitis.免疫检查点抑制剂相关性肺炎的临床诊断与治疗。
Thorac Cancer. 2020 Jan;11(1):191-197. doi: 10.1111/1759-7714.13240. Epub 2019 Nov 24.
7
Tyrosine kinase inhibitors and immune checkpoint inhibitors-induced thyroid disorders.酪氨酸激酶抑制剂和免疫检查点抑制剂引起的甲状腺疾病。
Crit Rev Oncol Hematol. 2019 Sep;141:23-35. doi: 10.1016/j.critrevonc.2019.05.015. Epub 2019 May 31.
8
Immune checkpoint inhibitor-induced Type 1 diabetes: a systematic review and meta-analysis.免疫检查点抑制剂相关 1 型糖尿病:系统评价和荟萃分析。
Diabet Med. 2019 Sep;36(9):1075-1081. doi: 10.1111/dme.14050. Epub 2019 Jul 7.
9
Treatment-Related Adverse Events of PD-1 and PD-L1 Inhibitors in Clinical Trials: A Systematic Review and Meta-analysis.临床试验中 PD-1 和 PD-L1 抑制剂的治疗相关不良反应:系统评价和荟萃分析。
JAMA Oncol. 2019 Jul 1;5(7):1008-1019. doi: 10.1001/jamaoncol.2019.0393.
10
The Relative Risk and Incidence of Immune Checkpoint Inhibitors Related Pneumonitis in Patients With Advanced Cancer: A Meta-Analysis.晚期癌症患者中免疫检查点抑制剂相关肺炎的相对风险和发病率:一项荟萃分析
Front Pharmacol. 2018 Dec 11;9:1430. doi: 10.3389/fphar.2018.01430. eCollection 2018.

肺癌患者严重化疗引起的周围神经病变的危险因素及生物标志物识别——一项回顾性病例系列研究

Identifying risk factors and biomarkers for severe CIP in lung cancer patients- a retrospective case series study.

作者信息

Wu Guixian, Qu Jingjing, Zheng Jing, Wu Binggen, Wang Ting, Gan Yuncui, Jiang Nan, Li Yuekang, Liu Jinpeng, Zhou Jianying, Zhou Jianya

机构信息

Department of Respiratory Disease, Thoracic Disease Center, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.

Department of Respiratory Disease, Taizhou Hospital of Zhejiang Province, Zhejiang University School of Medicine, Linhai, China.

出版信息

Immunotherapy. 2024;16(18-19):1131-1140. doi: 10.1080/1750743X.2024.2429369. Epub 2024 Nov 26.

DOI:10.1080/1750743X.2024.2429369
PMID:39589860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11633429/
Abstract

BACKGROUND

Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy, but they can induce immune-related adverse events, including immune checkpoint inhibitor-associated pneumonia (CIP), a severe lung complication. CIP, particularly Grades 3-4, is associated with poor prognosis, indicating a critical need for research on this issue. Our study aimed to investigate the risk factors and biomarkers associated with severe CIP in lung cancer patients treated with ICIs, where OS represents overall survival and PFS denotes progression-free survival.

METHODS

We conducted a retrospective analysis of 106 lung cancer patients with CIP at the First Affiliated Hospital of Zhejiang University from 2019 to 2023, categorized into four severity grades.

RESULTS

The median time to onset of CIP was 5.17 months. Patients with Grade 3-4 CIP had a median PFS of 6.5 months and OS of 11.2 months. Univariate analysis identified phosphocreatine kinase below 61.5 U/l, Forced Vital Capacity (FVC) below 1.96, and BMI below 21.26 as predictive factors for Grades 3-4 CIP. Multivariate analysis confirmed that a decreased FVC was a significant predictor.

CONCLUSIONS

A decreased FVC below 1.96 emerged as a predictive factor for Grades 3-4 CIP, highlighting the importance of monitoring FVC in patients receiving ICIs.

摘要

背景

免疫检查点抑制剂(ICIs)彻底改变了癌症治疗方式,但它们可引发免疫相关不良事件,包括免疫检查点抑制剂相关肺炎(CIP),这是一种严重的肺部并发症。CIP,尤其是3 - 4级,与预后不良相关,这表明对该问题进行研究至关重要。我们的研究旨在调查接受ICIs治疗的肺癌患者中与严重CIP相关的危险因素和生物标志物,其中总生存期用OS表示,无进展生存期用PFS表示。

方法

我们对2019年至2023年在浙江大学第一附属医院的106例患有CIP的肺癌患者进行了回顾性分析,将其分为四个严重程度等级。

结果

CIP的中位发病时间为5.17个月。3 - 4级CIP患者的中位PFS为6.5个月,中位OS为11.2个月。单因素分析确定磷酸肌酸激酶低于61.5 U/l、用力肺活量(FVC)低于1.96以及体重指数低于21.26为3 - 4级CIP的预测因素。多因素分析证实FVC降低是一个显著的预测因素。

结论

FVC低于1.96成为3 - 4级CIP的预测因素,突出了在接受ICIs治疗的患者中监测FVC的重要性。