Clinical factors associated with high PD-L1 expression in patients with early-stage non-small cell lung cancer

被引:0
作者
Ohara, Shuta [1 ]
Suda, Kenichi [1 ]
Hamada, Akira [1 ]
Chiba, Masato [1 ]
Ito, Masaoki [1 ]
Shimoji, Masaki [1 ]
Takemoto, Toshiki [1 ]
Soh, Junichi [1 ,2 ]
Tsutani, Yasuhiro [1 ]
机构
[1] Kindai Univ, Fac Med, Dept Surg, Div Thorac Surg, 377-2 Ohno Higashi, Osakasayama, 5898511, Japan
[2] Osaka Metropolitan Univ, Grad Sch Med, Dept Thorac Surg, Osaka, Japan
基金
日本学术振兴会;
关键词
non-small cell lung cancer; plasma fibrinogen; programmed cell death ligand 1; SUVmax; SINGLE-ARM; OPEN-LABEL; CHEMOTHERAPY; MULTICENTER;
D O I
10.1111/1759-7714.15453
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Superior outcomes have been obtained for neoadjuvant treatment with immune checkpoint inhibitors (ICI) plus chemotherapy over neoadjuvant chemotherapy alone, especially in patients with high programmed cell death ligand 1 (PD-L1) expression. However, it is not always possible to obtain sufficient tumor specimens for biomarker testing before surgery. In this study, we explored clinical factors that can predict high PD-L1 expression. Methods: We retrospectively enrolled 340 lung cancer patients who received pulmonary resection between 2014 and 2023 and who had PD-L1 expression data. Chi-squared tests and logistic regression analyses were used to identify clinical factors associated with high PD-L1 status. Results: Univariable and multivariable analyses revealed that smoking, high maximum standardized uptake value (SUVmax) of 18F-fluorodeoxyglucose positron emission computed tomography (18F-FDG PET/CT), and high plasma fibrinogen are independent predictors of high PD-L1 expression. A predictive score for high PD-L1 expression (ranging from 0 to 3) was developed based on these parameters. Notably, only 5% of patients with a score of 0 exhibited high PD-L1 expression, whereas this proportion increased to 53% for patients with a score of 3. Conclusion: These results showed that plasma fibrinogen, smoking history, and SUVmax are predictors of high PD-L1 expression, providing a basis for identifying patients expected to benefit from neoadjuvant ICI treatment.
引用
收藏
页码:2229 / 2234
页数:6
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