• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

接受第三代EGFR酪氨酸激酶抑制剂和胸部放疗的非小细胞肺癌患者放射性肺炎的危险因素。

Risk factors for radiation pneumonitis in NSCLC patients treated with third-generation EGFR TKIs and chest radiotherapy.

作者信息

Zhao Nan, Xiong Liang, Bai Xuehong, Pan Wenyan, Hai Ping, Ye Hongqiang, Zhao Ting, Cui Kai, Ma Rong, Wang Yanyang

机构信息

Master Training Station, General Hospital of Ningxia Medical University, Yinchuan, China.

Graduate School of Ningxia Medical University, Yinchuan, China.

出版信息

Radiat Oncol. 2025 May 9;20(1):72. doi: 10.1186/s13014-025-02649-0.

DOI:10.1186/s13014-025-02649-0
PMID:40346592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12065359/
Abstract

BACKGROUND

Non-small cell lung cancer (NSCLC) patients receiving third-generation EGFR TKIs with thoracic radiotherapy (TRT) significantly prolong survival and also increase the incidence of radiation pneumonitis (RP). The aim of our study was to investigate the incidence and risk factors of RP in NSCLC patients receiving third-generation EGFR TKIs and TRT.

PATIENTS AND METHODS

We retrospectively evaluated NSCLC patients who received both third-generation EGFR TKIs and TRT at the General Hospital of Ningxia Medical University from January 2023 to September 2024. RP was diagnosed by clinical symptoms on computed tomography (CT) scans and graded according to the Common Terminology Criteria for Adverse Events 5.0. Risk factors for RP were determined by univariate and multivariate logistic regression analysis.

RESULTS

Of the 42 patients included, 26 (61.9%) developed RP and 14 (33.3%) developed grade ≥ 2 RP. Grade ≥ 2 RP all occurred within 6 months of receiving TRT, and the median time from TRT to RP was 3.69 months (2-10 months). GTV ≥ 39 ml and total lung V20 ≥ 14.95% were found to be independent risk factors for RP development.

CONCLUSION

The strategy of combining a third-generation TKI with TRT significantly increases the incidence of RP, and the risk of RP in these patients can be reduced by adjusting lung radiation dosimetry parameters. In NSCLC patients taking triple-generation TKIs with primary tumour progression, the timing and dose of TRT addition must be strictly controlled to optimise the therapeutic strategy and reduce the incidence of RP.

CLINICAL TRIAL NUMBER

Not applicable.

摘要

背景

接受第三代表皮生长因子受体酪氨酸激酶抑制剂(EGFR TKIs)联合胸部放疗(TRT)的非小细胞肺癌(NSCLC)患者生存期显著延长,但放射性肺炎(RP)的发生率也会增加。我们研究的目的是调查接受第三代EGFR TKIs和TRT的NSCLC患者中RP的发生率及危险因素。

患者与方法

我们回顾性评估了2023年1月至2024年9月在宁夏医科大学总医院接受第三代EGFR TKIs和TRT的NSCLC患者。根据计算机断层扫描(CT)上的临床症状诊断RP,并按照不良事件通用术语标准5.0进行分级。通过单因素和多因素逻辑回归分析确定RP的危险因素。

结果

纳入的42例患者中,26例(61.9%)发生RP,14例(33.3%)发生≥2级RP。≥2级RP均发生在接受TRT的6个月内,从TRT到发生RP的中位时间为3.69个月(2 - 10个月)。发现肿瘤靶区(GTV)≥39 ml和全肺V20≥14.95%是发生RP的独立危险因素。

结论

第三代TKI联合TRT策略显著增加了RP的发生率,通过调整肺部放射剂量学参数可降低这些患者发生RP的风险。在接受三代TKIs且原发肿瘤进展的NSCLC患者中,必须严格控制加用TRT的时机和剂量,以优化治疗策略并降低RP的发生率。

临床试验编号

不适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/12065359/88de538964c6/13014_2025_2649_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/12065359/905d48c619f5/13014_2025_2649_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/12065359/88de538964c6/13014_2025_2649_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/12065359/905d48c619f5/13014_2025_2649_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/12065359/88de538964c6/13014_2025_2649_Fig2_HTML.jpg

相似文献

1
Risk factors for radiation pneumonitis in NSCLC patients treated with third-generation EGFR TKIs and chest radiotherapy.接受第三代EGFR酪氨酸激酶抑制剂和胸部放疗的非小细胞肺癌患者放射性肺炎的危险因素。
Radiat Oncol. 2025 May 9;20(1):72. doi: 10.1186/s13014-025-02649-0.
2
Overlap time is an independent risk factor of radiation pneumonitis for patients treated with simultaneous EGFR-TKI and thoracic radiotherapy.重叠时间是同时接受表皮生长因子受体酪氨酸激酶抑制剂和胸部放疗的患者放射性肺炎的独立危险因素。
Radiat Oncol. 2021 Feb 23;16(1):41. doi: 10.1186/s13014-021-01765-x.
3
Symptomatic Radiation Pneumonitis in NSCLC Patients Receiving EGFR-TKIs and Concurrent Once-daily Thoracic Radiotherapy: Predicting the Value of Clinical and Dose-volume Histogram Parameters.接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)联合每日一次胸部放疗的非小细胞肺癌(NSCLC)患者出现有症状的放射性肺炎:预测临床和剂量-体积直方图参数的价值。
Zhongguo Fei Ai Za Zhi. 2022 Jun 20;25(6):409-419. doi: 10.3779/j.issn.1009-3419.2022.102.17.
4
Radiation pneumonitis after concurrent aumolertinib and thoracic radiotherapy in EGFR-mutant non-small cell lung cancer patients.奥希替尼同步胸部放疗后致 EGFR 突变非小细胞肺癌患者放射性肺炎
BMC Cancer. 2024 Feb 12;24(1):197. doi: 10.1186/s12885-024-11946-y.
5
The incidence of and risk factors for radiation pneumonitis in patients treated with simultaneous bevacizumab and thoracic radiotherapy.同时使用贝伐珠单抗和胸部放疗治疗的患者中放射性肺炎的发生率和危险因素。
Radiat Oncol. 2024 May 30;19(1):67. doi: 10.1186/s13014-024-02458-x.
6
Radiation recall pneumonitis induced by epidermal growth factor receptor-tyrosine kinase inhibitor in patients with advanced nonsmall-cell lung cancer.表皮生长因子受体-酪氨酸激酶抑制剂诱发的晚期非小细胞肺癌患者放射性肺炎
J Chin Med Assoc. 2016 May;79(5):248-55. doi: 10.1016/j.jcma.2016.01.008. Epub 2016 Mar 29.
7
Thoracic Radiotherapy Improves the Survival in Patients With -Mutated Oligo-Organ Metastatic Non-Small Cell Lung Cancer Treated With Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors: A Multicenter, Randomized, Controlled, Phase III Trial.胸部放疗可改善接受表皮生长因子受体酪氨酸激酶抑制剂治疗的KRAS突变型寡器官转移非小细胞肺癌患者的生存率:一项多中心、随机、对照、III期试验。
J Clin Oncol. 2025 Feb;43(4):412-421. doi: 10.1200/JCO.23.02075. Epub 2024 Oct 7.
8
Efficacy and Safety of Third-Generation EGFR-TKIs Combined with Radiotherapy for Advanced NSCLC with Typical EGFR Mutations: A Retrospective Study.第三代表皮生长因子受体酪氨酸激酶抑制剂联合放疗治疗具有典型表皮生长因子受体突变的晚期非小细胞肺癌的疗效与安全性:一项回顾性研究
Curr Med Sci. 2025 Apr;45(2):280-287. doi: 10.1007/s11596-025-00032-4. Epub 2025 Mar 11.
9
Clinical outcomes and radiation pneumonitis after concurrent EGFR-tyrosine kinase inhibitors and radiotherapy for unresectable stage III non-small cell lung cancer.不可切除 III 期非小细胞肺癌同步 EGFR 酪氨酸激酶抑制剂和放疗的临床结果和放射性肺炎。
Thorac Cancer. 2021 Mar;12(6):814-823. doi: 10.1111/1759-7714.13816. Epub 2021 Jan 27.
10
Comparison of the Incidence Rate of Radiation Pneumonitis Observed in Patients with Advanced Lung Adenocarcinoma Treated with Simultaneous Thoracic Radiotherapy and 1G/2G/3G EGFR-TKIs.同步胸部放疗联合1G/2G/3G表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)治疗晚期肺腺癌患者放射性肺炎发生率的比较
Cancer Manag Res. 2023 Apr 12;15:351-362. doi: 10.2147/CMAR.S404874. eCollection 2023.

本文引用的文献

1
Pathogenic mechanisms and latest therapeutic approaches for radiation-induced lung injury: A narrative review.放射性肺损伤的发病机制及最新治疗方法:综述。
Crit Rev Oncol Hematol. 2024 Oct;202:104461. doi: 10.1016/j.critrevonc.2024.104461. Epub 2024 Aug 3.
2
Osimertinib Resistance via Histologic Transformation From Non-small Cell Lung Carcinoma to Carcinosarcoma.奥希替尼耐药:非小细胞肺癌组织学转化为癌肉瘤
Cureus. 2024 Apr 29;16(4):e59293. doi: 10.7759/cureus.59293. eCollection 2024 Apr.
3
Radiation pneumonitis after concurrent aumolertinib and thoracic radiotherapy in EGFR-mutant non-small cell lung cancer patients.
奥希替尼同步胸部放疗后致 EGFR 突变非小细胞肺癌患者放射性肺炎
BMC Cancer. 2024 Feb 12;24(1):197. doi: 10.1186/s12885-024-11946-y.
4
Localization of Sites of Osimertinib Action in Rat Intestine, Skin, and Lung by Immunohistochemistry.通过免疫组织化学法对奥希替尼在大鼠肠道、皮肤和肺中的作用位点进行定位。
Acta Histochem Cytochem. 2023 Dec 28;56(6):145-151. doi: 10.1267/ahc.23-00055. Epub 2023 Dec 23.
5
Salivary metabolites as novel independent predictors of radiation pneumonitis.唾液代谢物作为放射性肺炎的新型独立预测因子。
J Cancer Res Clin Oncol. 2023 Dec;149(19):17559-17566. doi: 10.1007/s00432-023-05479-3. Epub 2023 Oct 31.
6
EGFR-TKIs plus stereotactic body radiation therapy (SBRT) for stage IV Non-small cell lung cancer (NSCLC): A prospective, multicenter, randomized, controlled phase II study.表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)联合立体定向体部放疗(SBRT)治疗Ⅳ期非小细胞肺癌(NSCLC):一项前瞻性、多中心、随机、对照的 II 期研究。
Radiother Oncol. 2023 Jul;184:109681. doi: 10.1016/j.radonc.2023.109681. Epub 2023 Apr 25.
7
Histological Transformation after Acquired Resistance to the Third-Generation EGFR-TKI in Patients with Advanced -Mutant Lung Adenocarcinoma.晚期 - 突变肺腺癌患者对第三代 EGFR-TKI 获得性耐药后的组织学转化。
Medicina (Kaunas). 2022 Jul 8;58(7):908. doi: 10.3390/medicina58070908.
8
Osimertinib and anti-HER3 combination therapy engages immune dependent tumor toxicity via STING activation in trans.奥希替尼与抗 HER3 联合治疗通过 STING 激活发挥免疫依赖的肿瘤毒性作用。
Cell Death Dis. 2022 Mar 28;13(3):274. doi: 10.1038/s41419-022-04701-3.
9
Efficacy of Aumolertinib (HS-10296) in Patients With Advanced EGFR T790M+ NSCLC: Updated Post-National Medical Products Administration Approval Results From the APOLLO Registrational Trial.奥莫替尼(HS-10296)治疗晚期EGFR T790M+非小细胞肺癌患者的疗效:APOLLO注册试验中国家药品监督管理局批准后的更新结果
J Thorac Oncol. 2022 Mar;17(3):411-422. doi: 10.1016/j.jtho.2021.10.024. Epub 2021 Nov 19.
10
Osimertinib: A Review in Previously Untreated, EGFR Mutation-Positive, Advanced NSCLC.奥希替尼:在未经治疗的、EGFR 突变阳性的晚期 NSCLC 中的应用评价。
Target Oncol. 2021 Sep;16(5):687-695. doi: 10.1007/s11523-021-00839-w.