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分子靶向抗肿瘤药物的肺部毒性:单中心 10 年经验。

Pulmonary toxicities of molecular targeted antineoplastic agents: a single-center 10-year experience.

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Seoul Hospital, Seoul, Korea.

Department of Radiology, Soonchunhyang University Seoul Hospital, Seoul, Korea.

出版信息

Korean J Intern Med. 2021 May;36(3):689-698. doi: 10.3904/kjim.2020.295. Epub 2021 Jan 8.

DOI:10.3904/kjim.2020.295
PMID:33412778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8137409/
Abstract

BACKGROUND/AIMS: A better understanding of cancer cell biology has led to the discovery and development of several new targeted agents for cancer. These drugs are widely used in cancer treatment and have good toxicity profiles. However, some patients are extremely sensitive to these drugs and can develop severe toxicities. Among the toxicities, pulmonary complications are infrequent with most targeted therapies. This study aimed to identify the radiologic pulmonary complications in various targeted therapies and to analyze the characteristics of patients with pulmonary toxicity.

METHODS

We retrospectively reviewed the medical records and chest image findings of 644 patients who were treated with targeted antineoplastic agents at Soonchunhyang University Hospital between May 2005 and September 2014.

RESULTS

Of these 644 patients, 90 (14.0%) developed pulmonary complications as noted on chest computed tomography. Among these patients, 15 (2.3%) developed drug-related pulmonary toxicities. Treatment with targeted agents was discontinued in all patients, while 11 patients were simultaneously treated with glucocorticoids. Three patients died of drug-related pulmonary toxicity.

CONCLUSION

During targeted therapy, clinicians should assess for pulmonary toxicities and symptoms that occur with dyspnea. If drug-induced pulmonary toxicities are suspected, imaging studies should be performed immediately, and the possibility of variable radiological patterns should be considered. Discontinuing the use of implicated causative agents and treatment with glucocorticoids resulted in an improvement in both symptoms and imaging findings, but some patients still experienced fatal pulmonary toxicities.

摘要

背景/目的:对癌细胞生物学的深入了解,推动了多种新型癌症靶向药物的发现和发展。这些药物在癌症治疗中得到广泛应用,且具有良好的毒性特征。然而,部分患者对这些药物极其敏感,可能会产生严重的毒性。在这些毒性中,大多数靶向治疗的肺部并发症并不常见。本研究旨在确定各种靶向治疗中的放射学肺部并发症,并分析发生肺部毒性患者的特征。

方法

我们回顾性分析了 2005 年 5 月至 2014 年 9 月在韩国顺天乡大学医院接受靶向抗肿瘤药物治疗的 644 例患者的病历和胸部影像检查结果。

结果

644 例患者中,90 例(14.0%)经胸部计算机断层扫描(CT)确诊发生肺部并发症。其中,15 例(2.3%)发生药物相关性肺毒性。所有患者均停止使用靶向药物治疗,同时 11 例患者接受糖皮质激素治疗。3 例患者死于药物相关性肺毒性。

结论

在靶向治疗期间,临床医生应评估是否出现呼吸困难等肺部毒性和症状。如果怀疑为药物诱导性肺毒性,应立即进行影像学检查,并考虑可能存在多种影像学表现。停止使用可疑致病药物并使用糖皮质激素治疗可改善症状和影像学表现,但部分患者仍会发生致命性肺部毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0326/8137409/920e42c6ff5b/kjim-2020-295f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0326/8137409/920e42c6ff5b/kjim-2020-295f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0326/8137409/920e42c6ff5b/kjim-2020-295f1.jpg

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Drug-induced interstitial lung disease in tyrosine kinase inhibitor therapy for non-small cell lung cancer: a review on current insight.酪氨酸激酶抑制剂治疗非小细胞肺癌所致药物性间质性肺疾病:当前认识的综述。
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