间质性肺疾病患者血清肿瘤相关抗原升高:临床特征和预后的回顾性研究

Expert review of respiratory medicine Pub Date : 2025-04-01 Epub Date: 2025-03-06 DOI:10.1080/17476348.2025.2473480
Yanling Ding, Yahong Chen, Ming Chen, Yi Liu, Nan Li, Yongchang Sun
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引用次数: 0

摘要

背景:据报道,血清肿瘤相关抗原(TAAs)升高在间质性肺疾病(ILD)患者中很常见,并与肺部受累或恶性肿瘤发展相关。然而,对于中国患者TAAs升高与各种类型ILDs之间的关系,尚无足够的纵向研究。研究设计和方法:回顾性纳入treatment-naïve ILD患者。分析比较正常与不同数量TAAs升高患者的临床、实验室、影像学特征及预后。结果:308例患者中有169例(54.87%)出现至少1例TAA升高。基线肺泡和间质评分都要高得多,在随访期间,两次和三次或更多taa升高的患者的肺部受累程度往往比正常taa患者更严重。随访期间,有三个或三个以上TAA升高的患者的间质评分最高,全因死亡率也高于只有一个TAA升高或TAA正常的患者。所有患者的恶性肿瘤发生率相似。结论:54.87%的ILD患者存在TAAs升高,且与肺间质病变相关,这可能是ILD患者肺部累及进展的标志,而不是恶性发展的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elevated serum tumor-associated antigens in patients with interstitial lung disease: a retrospective study on clinical features and prognosis.

Background: Elevated serum tumor-associated antigens (TAAs) were reported to be common in patients with interstitial lung disease (ILD) and correlated with pulmonary involvement or malignancy development. However, there were no adequate longitudinal studies on the association between elevated TAAs and various types of ILDs in Chinese patients.

Research design and methods: The treatment-naïve ILD patients were retrospectively enrolled. The clinical, laboratory, imaging characteristics, and prognosis were analyzed and compared among those with normal and different number of elevated TAAs.

Results: An increase of at least one TAA was present in 169/308 (54.87%) of our patients. Both baseline alveolar and interstitial scores were much higher, and lung involvement tended to be worse during follow-up in patients with two and three or more elevated TAAs than in normal TAAs. Patients with three or more elevated TAAs had the highest interstitial scores and a higher all-cause mortality during follow-up than those with one elevated TAA or normal TAAs. The occurrence of malignancy was similar in all patients.

Conclusion: Elevated TAAs were present in 54.87% of ILD patients and associated with lung interstitial lesions, which might be a marker for lung involvement progression, while not for malignancy development in ILD.

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