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
  • [31] The clinical significance of autophagy in patients with non-small cell lung cancer
    Nakashima, Nariyasu
    Liu, Dage
    Nakano, Takayuki
    Go, Tetsuhiko
    Yokomise, Hiroyasu
    CANCER SCIENCE, 2018, 109 : 1425 - 1425
  • [32] Clinical Significance of Expression of Periostin in Non-small Cell Lung Cancer
    Qiao, Zhixiong
    Zhang, Lan
    He, Jinxi
    He, Wei
    JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN, 2022, 32 (09): : 1149 - 1153
  • [33] Clinical significance of aminopeptidase N in non-small cell lung cancer
    Tokuhara, Takahiro
    Hattori, Noboru
    Ishida, Hisao
    Hirai, Tatsuya
    Higashiyama, Masahiko
    Kodama, Ken
    Miyake, Masayuki
    CLINICAL CANCER RESEARCH, 2006, 12 (13) : 3971 - 3978
  • [34] Prognostic impact of CXCL16 and CXCR6 in non-small cell lung cancer: combined high CXCL16 expression in tumor stroma and cancer cells yields improved survival (vol 15, 441, 2015)
    Hald, Sigurd M.
    Kiselev, Yury
    Al-Saad, Samer
    Richardsen, Elin
    Johannessen, Charles
    Eilertsen, Marte
    Kilvaer, Thomas K.
    Al-Shibli, Khalid
    Andersen, Sigve
    Busund, Lill-Tove
    Bremnes, Roy M.
    Donnem, Tom
    BMC CANCER, 2016, 16
  • [35] Clinical significance of pretreatment tumor growth rate for locally advanced non-small cell lung cancer
    Osorio, Benedict
    Yegya-Raman, Nikhil
    Kim, Sinae
    Simone, Charles B., II
    Ross, Christina Theodorou
    Deek, Matthew P.
    Gaines, Dakim
    Zou, Wei
    Lin, Liyong
    Malhotra, Jyoti
    Nie, Ke
    Aisner, Joseph
    Jabbour, Salma K.
    ANNALS OF TRANSLATIONAL MEDICINE, 2019, 7 (05)
  • [36] Gefitinib or Erlotinib in the Treatment of Advanced Non-small Cell Lung Cancer
    Shao, Yu-Yun
    Lin, Chia-Chi
    Yang, Chih-Hsin
    DISCOVERY MEDICINE, 2010, 9 (49) : 538 - 545
  • [37] CRIZOTINIB FOR THE TREATMENT OF PATIENTS WITH ADVANCED NON-SMALL CELL LUNG CANCER
    Bowles, D. W.
    Weickhardt, A. J.
    Doebele, R. C.
    Camidge, D. R.
    Jimeno, A.
    DRUGS OF TODAY, 2012, 48 (04) : 271 - 282
  • [38] Novel immunotherapy in the treatment of advanced non-small cell lung cancer
    Santabarbara, G.
    Maione, P.
    Rossi, A.
    Palazzolo, G.
    Gridelli, C.
    EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2016, 9 (12) : 1571 - 1581
  • [39] Treatment of Advanced-Stage Non-Small Cell Lung Cancer
    Gesthalter, Yaron
    Smyth, Robert
    Sullivan, Donald
    Kathuria, Hasmeena
    Sockrider, Marianna
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2022, 205 (05)
  • [40] A Decade of Advances in Treatment for Advanced Non-Small Cell Lung Cancer
    Gettinger, Scott
    Lynch, Thomas
    CLINICS IN CHEST MEDICINE, 2011, 32 (04) : 839 - +