| Literature DB >> 25279192 |
Daisuke Yamada1, Hirokazu Matsushita2, Takeshi Azuma3, Tohru Nakagawa3, Masayoshi Nagata4, Yukio Yamada3, Motofumi Suzuki5, Tetsuya Fujimura3, Hiroshi Fukuhara3, Haruki Kume3, Yukio Homma3, Kazuhiro Kakimi2.
Abstract
This prospective study was conducted to identify predictive markers for the response of metastatic renal cell carcinoma (RCC) to tyrosine kinase inhibitors (TKIs). Patients with histologically proven RCC with at least one measurable metastatic lesion were enrolled in this study. Blood samples were collected prior to treatment and the plasma levels of 27 cytokines were measured. Tumor response was assessed 8-12 weeks after the initiation of TKI treatment. A total of 13 patients (11 men and 2 women) with a median age of 63 years received sunitinib (8 cases), sorafenib (1 case), or axitinib (4 cases). Partial response (PR) was achieved in 5 patients (38%), stable disease (SD) in 4 (30%) and progressive disease (PD) was noted in 4 (30%). The plasma granulocyte macrophage colony-stimulating factor (GM-CSF) level in PR cases was significantly higher compared to that in SD or PD cases (P=0.012). Therefore, GM-CSF may be a predictive biomarker of the response of RCC to TKI treatment, suggesting that TKIs may exert clinical effects not only through suppression of the vascular endothelial growth factor, but also through immune system modulation.Entities:
Keywords: granulocyte macrophage colony-stimulating factor; metastatic; renal cell carcinoma; tyrosine kinase inhibitors
Year: 2014 PMID: 25279192 PMCID: PMC4179789 DOI: 10.3892/mco.2014.360
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450