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dc.contributor.authorKargi, Aysegul
dc.contributor.authorYalcin, Arzu Didem
dc.contributor.authorErin, Nuray
dc.contributor.authorSavas, Burhan
dc.contributor.authorPolat, H. Huseyin
dc.contributor.authorGorczynski, Reginald M.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:04:29Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:04:29Z
dc.date.issued2012
dc.identifier.issn1433-6510
dc.identifier.urihttps://hdl.handle.net/20.500.12418/9331
dc.descriptionWOS: 000305711100017en_US
dc.descriptionPubMed ID: 22783581en_US
dc.description.abstractBackground: Colorectal cancer is the third most common human cancer and the third leading cause of cancer related death. BevacizumAb is a humanized monoclonal antibody developed against vascular endothelial growth factor (VEGF) for the treatment of metastatic cancers. Our goal was to evaluate the possibility of using serum sTRAIL and IL8 as markers of treatment efficacy and prognosis in patients with metastatic colon cancer. Methods: The study was conducted in Denizli between November 10, 2009 and September 20, 2010. 25 patients (6 female, 19 male) with metastatic colon cancer whose mean age was 58.7 years, were selected and included in the study. All patients received therapy with BevacizumAb. All patients were followed in the Oncology Clinic of Denizli State Hospital and were evaluated by clinical status. sTRAIL and IL8 levels were measured by ELISA in the sera of 25 BevacizumAb treated metastatic colon cancer patients and 20 healthy age-gender matched controls. Measurements were taken before and after treatment. Results: The serum sTRAIL concentrations in patients before therapy were similar to those of healthy age-gender matched controls, namely 1.23 +/- 0.06 ng/mL and 1.21 +/- 0.04 ng/mL, respectively. After BevacizumAb treatment, sTRAIL ratios were increased significantly in 11 of 25 patients. 14 patients showed progressive disease with median overall survival of only 8.1 +/- 0.4 months. These 14 patients were the same ones who showed no increase in sTRAIL levels after BevacizumAb treatment. We explored evidence for a correlation between sTRAIL levels and overall survival rates and observed that elevated sTRAIL levels after the BevacizumAb treatment were significantly associated with increased median overall survival up to 22.6 months. Serum IL8 levels were decreased in all patients who received BevacizumAb therapy. Conclusions: In BevacizumAb therapy, serum IL8 levels were decreased in all patients, and thus, changes in such levels were not correlated with disease outcome. Our data suggest measurement of changes in sTRAIL following BevacizumAb treatment may have prognostic value in metastatic colon cancer patients. (Clin. Lab. 2012;58:501-505)en_US
dc.language.isoengen_US
dc.publisherCLIN LAB PUBLen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAnti-VEGF monoclonal antibodyen_US
dc.subjectBevacizumAben_US
dc.subjectIL8en_US
dc.subjectsTRAILen_US
dc.titleIL8 and Serum Soluble TRAIL Levels Following Anti-VEGF Monoclonal Antibody Treatment in Patients with Metastatic Colon Canceren_US
dc.typearticleen_US
dc.relation.journalCLINICAL LABORATORYen_US
dc.contributor.department[Gorczynski, Reginald M.] Univ Hlth Network, Div Cellular & Mol Biol, Toronto Hosp, Toronto, ON, Canada -- [Kargi, Aysegul] Denizli Educ & Res Hosp, Oncol Unit, Denizli, Turkey -- [Yalcin, Arzu Didem] Antalya Educ & Res Hosp, Allergol & Clin Immunol Unit, Antalya, Turkey -- [Erin, Nuray] Akdeniz Univ, Fac Med, Dept Pharmacol, TR-07058 Antalya, Turkey -- [Savas, Burhan] Akdeniz Univ, Fac Med, Dept Med Oncol, TR-07058 Antalya, Turkey -- [Polat, H. Huseyin] Cumhuriyet Univ, Dept Publ Hlth, Fac Med, TR-58140 Sivas, Turkeyen_US
dc.contributor.authorIDErin, Nuray -- 0000-0002-6116-1970en_US
dc.identifier.volume58en_US
dc.identifier.issue05.Junen_US
dc.identifier.endpage505en_US
dc.identifier.startpage501en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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