The clinical significance of CXCL16 in the treatment of advanced non-small cell lung cancer

被引:11
|
作者
Shibata, Yuji [1 ]
Kobayashi, Nobuaki [1 ]
Sato, Takashi [1 ,2 ]
Nakashima, Kentaro [1 ]
Kaneko, Takeshi [1 ]
机构
[1] Yokohama City Univ, Dept Pulmonol, Grad Sch Med, Yokohama, Kanagawa, Japan
[2] Shinshu Univ, Inst Biomed Sci, Kamiina, Japan
关键词
Bevacizumab; CXCL16; non-small cell lung cancer; VEGF; CHEMOKINE CXCL16; PROSTATE-CANCER; BEVACIZUMAB; EXPRESSION; ANGIOGENESIS; PROGRESSION; METASTASIS; REGULATOR; HYPOXIA; GROWTH;
D O I
10.1111/1759-7714.13387
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Bevacizumab, a monoclonal antibody against vascular endothelial growth factor (VEGF)-A, has shown efficacy in patients with advanced nonsquamous non-small cell lung cancer (NSCLC). There are no identified or clinically validated biomarkers to determine the efficacy of bevacizumab. In this study, we assessed the adequacy of chemokine (C-X-C motif) ligand 16 (CXCL16) as a biomarker for patients treated with bevacizumab-containing chemotherapy regimen. Methods Patients diagnosed histologically with NSCLC were enrolled. Serial serum CXCL16 levels during treatment were measured by enzyme-linked immunosorbent assay. The relationship between serum CXCL16 levels before and after treatment, progression-free survival, and overall survival were analyzed. CXCL16 and VEGF-A expressions in lung cancer tissue were also evaluated by immunohistochemical tests. Results The median serum level of CXCL16 in these patients was 3.4 ng/mL, which was significantly higher than that in age-matched healthy adults (2.2 ng/mL). Immunohistochemistry results showed that CXCL16 was predominantly localized in the tumor stroma, whereas VEGF was expressed in tumor cells. Including bevacizumab with chemotherapy led to lower CXCL16 levels post-chemotherapy, which correlated with better response rates. In addition, evaluation of differences in serum CXCL16 levels before and after the first-line chemotherapy showed that longer overall survival was achieved in patients who showed a larger decrease in serum CXCL16 levels. Conclusions According to our findings, serum CXCL16 level was identified as a potential biomarker for the efficacy of therapy, including anti-VEGF. Key points Significant findings of the study Patients with NSCLC whose serum CXCL16 levels decreased below 0.07 ng/mL after chemotherapy, showed longer overall survival than those without this decrease. Moreover, low CXCL16 levels corresponded to better response rates among patients with advanced NSCLC treated with bevacizumab-containing chemotherapy. What this study adds Previously there were no identifiable predictive biomarkers to determine the efficacy of bevacizumab. Data from our findings identified serum CXCL16 level as a potential biomarker for the efficacy of bevacizumab-containing chemotherapy.
引用
收藏
页码:1258 / 1264
页数:7
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