ICAM-1 expression in patients with advanced non-small cell lung cancer treated with radiotherapy

被引:4
|
作者
Gkogkou, Pinelopi [1 ]
Peponi, Evangelia [2 ]
Ntaskagiannis, Dimitrios [2 ]
Demou, Asimo [3 ]
Ioakeim, Elli [3 ]
Evangelos, Briasoulis [4 ,5 ]
Tsekeris, Periklis [2 ]
机构
[1] Norfolk & Norwich Univ Hosp, Oncol Dept, Conley Lane, Norwich NR4 7UY, Norfolk, England
[2] Univ Hosp Ioannina, Dept Oncol, Stavros Niarchos Ave 1, Ioannina 45500, Greece
[3] Hatzikosta Commun Hosp, Dept Pathol, Makrygianni Ave, Ioannina 45001, Greece
[4] Univ Ioannina, Canc Biobank Ctr, Hematol Dept, Univ Campus, Ioannina 45110, Greece
[5] Univ Ioannina, Canc Biobank Ctr, Intersci Mol Lab, Univ Campus, Ioannina 45110, Greece
来源
JOURNAL OF BUON | 2020年 / 25卷 / 04期
关键词
ICAM; immunohistochemistry; non-small cell lung cancer; radiotherapy; INTERCELLULAR-ADHESION MOLECULE-1; ENDOTHELIAL GROWTH-FACTOR; INVASION; BREAST; CD54;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the possible clinical relevance of ICAM-1 molecule in patients with advanced non-small cell lung cancer (NSCLC) treated with radiotherapy. Methods: The expression of ICAM-1 was examined immunohistochemically on tissue specimens of 62 patients with pathologically confirmed NCSLC. The median age at diagnosis was 62 years (range 49-84) with a male predominance (87.8%). All patients had stage III disease at presentation. The median follow up was 15.5 months (range 7-44). Obtained expression data were weighted against clinical and pathological parameters. Results: Thirty-seven patients (60%) had no ICAM-1 staining, 16 patients (26%) had weak staining, while 6 patients (10%) expressed moderate staining and only 3 patients (5%) showed strong ICAM-1 staining. Moderate and high expressions were mostly observed in adenocarcinomas and undifferentiated carcinomas (n=8), that are considered more aggressive than squamous cell carcinoma (n=1). The median overall survival (OS) was 15 months (range 11-20). There seemed to exist an inverse association between ICAM-1 expression and OS, since there was a trend in median survival in favor of no ICAM-1 expression (p=0.083). Moreover, in patients with no ICAM-1 expression, there was observed a statistically significant difference in OS, favoring the squamous cell subtype (p=0.006). Nevertheless, ICAM-1 expression did not confer any statistical significance regarding smoking status (p=0.128), metastatic potential (p=0.574) as well as with the site of metastasis (p=0.964). Conclusion: Our findings may serve as a helping resource for further investigations of ICAM-1 as a molecular marker that could characterize treatment response and survival of tumor subpopulations.
引用
收藏
页码:1779 / 1783
页数:5
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