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
相关论文
共 50 条
  • [41] Is there a standard treatment for locally advanced non-small cell lung cancer?
    Buccheri, G
    CHEST, 1996, 109 (04) : 864 - 866
  • [42] Ramucirumab for the treatment of advanced or metastatic non-small cell lung cancer
    Takeda, Koji
    Daga, Haruko
    EXPERT OPINION ON BIOLOGICAL THERAPY, 2016, 16 (12) : 1541 - 1547
  • [43] A Paradigm Shift in the Treatment of Advanced Non-Small Cell Lung Cancer
    Varughese, Shibu
    Jahangir, K. Saad
    Simpson, Catherine E.
    Boulmay, Brian C.
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2012, 344 (02): : 147 - 150
  • [44] The safety of nivolumab for the treatment of advanced non-small cell lung cancer
    Metro, Giulio
    Ricciuti, Biagio
    Brambilla, Marta
    Baglivo, Sara
    Soli, Irene
    Minenza, Elisa
    Leonardi, Giulia Costanza
    D'arpino, Alessandro
    Colabrese, Daniela
    Tazza, Marco
    Zicari, Daniela
    Minotti, Vincenzo
    Chiari, Rita
    EXPERT OPINION ON DRUG SAFETY, 2017, 16 (01) : 101 - 109
  • [45] IMPROVING TREATMENT OF ADVANCED NON-SMALL CELL LUNG CANCER (NSCLC)
    Reck, M.
    ANTICANCER RESEARCH, 2008, 28 (6B) : 4038 - 4038
  • [46] TREATMENT OF ADVANCED NON-SMALL CELL LUNG-CANCER WITH BISANTRENE
    FUKS, JZ
    VANECHO, DA
    GARBINO, C
    KASDORF, H
    AISNER, J
    CANCER TREATMENT REPORTS, 1983, 67 (06): : 597 - 598
  • [47] Immunotherapy in treatment naive advanced non-small cell lung cancer
    Ernani, Vinicius
    Ganti, Apar Kishor
    JOURNAL OF THORACIC DISEASE, 2018, 10 : S412 - S421
  • [48] The emerging treatment landscape of advanced non-small cell lung cancer
    Economopoulou, Panagiota
    Mountzios, Giannis
    ANNALS OF TRANSLATIONAL MEDICINE, 2018, 6 (08)
  • [49] ERLOTINIB IN ADVANCED NON-SMALL CELL LUNG CANCER (NSCLC) TREATMENT
    Goncalves, Ivone M.
    Monteiro, Regina
    Neves, Sofia
    Conde, Sara
    Campainha, Sergio
    Parente, Barbara
    JOURNAL OF THORACIC ONCOLOGY, 2011, 6 (06) : S1298 - S1298
  • [50] Salvage treatment with anlotinib for advanced non-small cell lung cancer
    Wu, Di
    Nie, Jun
    Dai, Ling
    Hu, Weiheng
    Zhang, Jie
    Chen, Xiaoling
    Ma, Xiangjuan
    Tian, Guangming
    Han, Jindi
    Han, Sen
    Long, Jieran
    Wang, Yang
    Zhang, Ziran
    Fang, Jian
    THORACIC CANCER, 2019, 10 (07) : 1590 - 1596