Browsing by Author "Savic-Vujovic, Katarina (57217857650)"
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Publication Biomarkers and Predictors of Adverse Cardiovascular Events in Different Stages of Chronic Kidney Disease(2022) ;Stopic, Bojan (57190427195) ;Medic-Brkic, Branislava (56029608400) ;Savic-Vujovic, Katarina (57217857650) ;Davidovic, Zeljko (26647384000) ;Todorovic, Jovana (7003376825)Dimkovic, Nada (6603958094)Chronic kidney disease (CKD) is an important factor that contributes to the increase of all-cause morbidity and mortality in the group of non-communicable diseases, and it is also recognized as a strong and independent risk factor that contributes to cardiovascular disease (CVD). CVDs are a consequence of the action of a large number of risk factors among which are traditional and non-traditional. These risk factors have been the subject of a large number of studies which partially explained the unfavorable cardiovascular (CV) outcome of CKD patients. Therefore, valid studies about clinical and biohumoral predictors are of particular importance, especially in the early stages of renal disease, that is, in patients with creatinine clearance below 60 ml/min/1.73 m2 when preventive measures are most effective. Among potential predictors of adverse CV outcome are biomarkers of inflammation (Interleukin-18—IL-18), oxidative stress (ischemia-modified albumin—IMA; superoxide dismutase—SOD), acute kidney injury (kidney injury molecule-1—KIM-1; neutrophil gelatinase–associated lipocalin—NGAL), and microribonucleic acids (specific microRNA-133a). In this review, we tried to confirm the relationship between risk factors of CKD and CVD and newer, less frequently examined biomarkers with the occurrence of incidental CV events in renal patients. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Biomarkers and Predictors of Adverse Cardiovascular Events in Different Stages of Chronic Kidney Disease(2022) ;Stopic, Bojan (57190427195) ;Medic-Brkic, Branislava (56029608400) ;Savic-Vujovic, Katarina (57217857650) ;Davidovic, Zeljko (26647384000) ;Todorovic, Jovana (7003376825)Dimkovic, Nada (6603958094)Chronic kidney disease (CKD) is an important factor that contributes to the increase of all-cause morbidity and mortality in the group of non-communicable diseases, and it is also recognized as a strong and independent risk factor that contributes to cardiovascular disease (CVD). CVDs are a consequence of the action of a large number of risk factors among which are traditional and non-traditional. These risk factors have been the subject of a large number of studies which partially explained the unfavorable cardiovascular (CV) outcome of CKD patients. Therefore, valid studies about clinical and biohumoral predictors are of particular importance, especially in the early stages of renal disease, that is, in patients with creatinine clearance below 60 ml/min/1.73 m2 when preventive measures are most effective. Among potential predictors of adverse CV outcome are biomarkers of inflammation (Interleukin-18—IL-18), oxidative stress (ischemia-modified albumin—IMA; superoxide dismutase—SOD), acute kidney injury (kidney injury molecule-1—KIM-1; neutrophil gelatinase–associated lipocalin—NGAL), and microribonucleic acids (specific microRNA-133a). In this review, we tried to confirm the relationship between risk factors of CKD and CVD and newer, less frequently examined biomarkers with the occurrence of incidental CV events in renal patients. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma(2022) ;Jokic, Vera (59900229100) ;Savic-Vujovic, Katarina (57217857650) ;Spasic, Jelena (57195299847) ;Bukumiric, Zoran (36600111200) ;Marinkovic, Mladen (57222259689) ;Radosavljevic, Davorin (55851649000)Cavic, Milena (39760938900)Background: The aim of this research was to evaluate clinical and low-cost genetic determinants of treatment outcome in EGFR mutation positive advanced lung adenocarcinoma patients. Material and Methods: EGFR mutation testing and EGFR 181946C>T genotyping were performed in 101 advanced lung adenocarcinoma patients using qRT-PCR and PCR-RFLP, respectively. Progression-free survival was defined as the time from the start of TKI therapy to date of progression, and overall survival as the time from diagnosis to death from any cause. Pain level was evaluated using a Numerical Rating Scale and the Verbal Descriptor Scale. Statistical significance was considered for P <.05. Results: Patients were treated with EGFR-TKIs for a period of 1–39months (median 9), with a median PFS of 12.0 months (10.4-13.6, CI 95%), and a median OS of 19.0 months (15.1-22.7, CI 95%). The presence of pain was significantly correlated with the existence of bone (P <.001) and adrenal glands metastases (P =.029). Genetic factors did not have a direct impact on pain management but had a significant effect on the response to TKIs leading to pain alleviation. Conclusions: EGFR mutation subtype and the EGFR 181946 C>T SNP had a significant effect on the response to TKI inducing an indirect anti-dolorous effect. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma(2022) ;Jokic, Vera (59900229100) ;Savic-Vujovic, Katarina (57217857650) ;Spasic, Jelena (57195299847) ;Bukumiric, Zoran (36600111200) ;Marinkovic, Mladen (57222259689) ;Radosavljevic, Davorin (55851649000)Cavic, Milena (39760938900)Background: The aim of this research was to evaluate clinical and low-cost genetic determinants of treatment outcome in EGFR mutation positive advanced lung adenocarcinoma patients. Material and Methods: EGFR mutation testing and EGFR 181946C>T genotyping were performed in 101 advanced lung adenocarcinoma patients using qRT-PCR and PCR-RFLP, respectively. Progression-free survival was defined as the time from the start of TKI therapy to date of progression, and overall survival as the time from diagnosis to death from any cause. Pain level was evaluated using a Numerical Rating Scale and the Verbal Descriptor Scale. Statistical significance was considered for P <.05. Results: Patients were treated with EGFR-TKIs for a period of 1–39months (median 9), with a median PFS of 12.0 months (10.4-13.6, CI 95%), and a median OS of 19.0 months (15.1-22.7, CI 95%). The presence of pain was significantly correlated with the existence of bone (P <.001) and adrenal glands metastases (P =.029). Genetic factors did not have a direct impact on pain management but had a significant effect on the response to TKIs leading to pain alleviation. Conclusions: EGFR mutation subtype and the EGFR 181946 C>T SNP had a significant effect on the response to TKI inducing an indirect anti-dolorous effect. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Hematological parameters in EGFR-mutated advanced NSCLC patients treated with TKIs: predicting survival and toxicity(2021) ;Jokic, Vera (59900229100) ;Savic-Vujovic, Katarina (57217857650) ;Spasic, Jelena (57195299847) ;Stanic, Nemanja (57195304019) ;Marinkovic, Mladen (57222259689) ;Radosavljevic, Davorin (55851649000)Cavic, Milena (39760938900)Background: The aim of this study was to analyze the prognostic value of pre-treatment hematological parameters in EGFR-mutated non-small cell lung cancer patients treated with tyrosine-kinase inhibitors (TKIs). Patients and methods: Patients with EGFR mutations were treated with EGFR-TKIs in the first line until progression/unacceptable toxicity. Hematological parameters were derived from the absolute baseline differential counts of a complete blood count. The associations between the patients’ and tumor characteristics were analyzed using Pearson Chi-Square, Fisher’s exact, t-test, and Mann–Whitney tests. Cutoff values were determined using ROC curves, and correlation with survival was examined by Kaplan–Meier method and Cox regression. Results: Patients with NMR<12.62 had a longer PFS compared to patients with higher NMR values (12.0 vs. 10.0 months, p = 0.054) and a significantly longer OS (20.0 vs. 11.0 months, p = 0.010). The same parameter was confirmed as a predictors of favorable response in the patient subgroup with activating EGFR mutations. Patients with NLR>2.9 and LMR<2.5 more often presented with paronichia and diarrhea, and patients with PLR>190 more often had paronichia, diarrhea and hyperbilirubinemia. Conclusion: Low baseline value of the hematological parameter NMR has shown potential as a routine, low-cost, and minimally invasive predictor of survival in EGFR-TKI-treated NSCLC patients. © 2021 Informa UK Limited, trading as Taylor & Francis Group. - Some of the metrics are blocked by yourconsent settings
Publication Immune Cell and Biochemical Biomarkers in Advanced Laryngeal Cancer(2022) ;Jotic, Ana (35173257500) ;Milovanovic, Jovica (6603250148) ;Savic-Vujovic, Katarina (57217857650) ;Radin, Zorana (57208752128) ;Medic, Branislava (56029608400) ;Folic, Miljan (56497240500) ;Pavlovic, Bojan (8212822900) ;Vujovic, Aleksandar (57190496164)Dundjerovic, Dusko (56515503700)Objective: The aim of this study was to evaluate cell and biochemical biomarkers and establish their prognostic value in patients with advanced laryngeal cancer. Material and Methods: A prospective study included 52 patients with advanced laryngeal carcinoma surgically treated at the tertiary referral center. Tumor tissue was immunohistochemically stained for T-cell markers (CD4 and CD8), and levels of cytokines (IL-6 and IL-8) and C-reactive protein were analyzed from blood samples. Results: Overall 3-year survival (OS) of patients included in the study was 69.2% and the disease specific survival (DSS) 72.5%. Higher expression of CD4+ and CD8+ were significant prognostic factors with positive impact on both OS and DSS in univariate analysis, but not in multivariate analysis. Levels of IL-8 were a significant predictor of 3-year OS and DSS survival in patients with advanced laryngeal cancer but not levels of IL-6 and CRP values. Conclusion: Though high expression of CD4 and CD8 were demonstrated in the tumor tissue, but their prognostic role was not established. Higher values of IL-8 proved to be significant negative predictor of DSS. This could further collaborate the inclusion of combination of biomarkers in assessment of favorable treatment choice in patients with advanced laryngeal carcinoma. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Immune Cell and Biochemical Biomarkers in Advanced Laryngeal Cancer(2022) ;Jotic, Ana (35173257500) ;Milovanovic, Jovica (6603250148) ;Savic-Vujovic, Katarina (57217857650) ;Radin, Zorana (57208752128) ;Medic, Branislava (56029608400) ;Folic, Miljan (56497240500) ;Pavlovic, Bojan (8212822900) ;Vujovic, Aleksandar (57190496164)Dundjerovic, Dusko (56515503700)Objective: The aim of this study was to evaluate cell and biochemical biomarkers and establish their prognostic value in patients with advanced laryngeal cancer. Material and Methods: A prospective study included 52 patients with advanced laryngeal carcinoma surgically treated at the tertiary referral center. Tumor tissue was immunohistochemically stained for T-cell markers (CD4 and CD8), and levels of cytokines (IL-6 and IL-8) and C-reactive protein were analyzed from blood samples. Results: Overall 3-year survival (OS) of patients included in the study was 69.2% and the disease specific survival (DSS) 72.5%. Higher expression of CD4+ and CD8+ were significant prognostic factors with positive impact on both OS and DSS in univariate analysis, but not in multivariate analysis. Levels of IL-8 were a significant predictor of 3-year OS and DSS survival in patients with advanced laryngeal cancer but not levels of IL-6 and CRP values. Conclusion: Though high expression of CD4 and CD8 were demonstrated in the tumor tissue, but their prognostic role was not established. Higher values of IL-8 proved to be significant negative predictor of DSS. This could further collaborate the inclusion of combination of biomarkers in assessment of favorable treatment choice in patients with advanced laryngeal carcinoma. © The Author(s) 2022. - Some of the metrics are blocked by yourconsent settings
Publication Survival outcomes in surgically treated patients with advanced laryngeal cancer in Serbia(2020) ;Milovanovic, Jovica (6603250148) ;Jotic, Ana (35173257500) ;Vidovic, Ljiljana Tesic (57016646300) ;Djukic, Vojko (6701658274) ;Trivic, Aleksandar (8301162500) ;Trivic, Sanja Krejovic (55346592200) ;Radin, Zorana (57208752128) ;Savic-Vujovic, Katarina (57217857650) ;Milovanovic, Andjela (57213394852) ;Banko, Bojan (35809871900)Artiko, Vera (55887737000)Background/Aim. Laryngeal carcinomas make 1%-3% of all head and neck malignancies.Treatment outcome and survival rates depend greatly on established stage of the disease. The purpose of this study was to examine the survival of the patients with advanced laryngeal carcinoma depending on gender, age, common risk factors (tobacco and alcohol use), primary tumor localization, histopathological tumor grade, clinical TNM (tumor, node and metastasis) stage and surgical treatment of the disease. Methods. Retrospective study included 252 patients treated surgically for advanced squamocellular carcinoma of the larynx in a threeyear period with five-year follow-up. Patients included in the study were treated primary with surgery, with postoperative radiotherapy and chemotherapy depending on the stage of the disease, intraoperative findings and tumor resection borders. Overall survival and disease-specific five-year survival of patients was calculated for demographical and clinical characteristics of the patients. Results. Overall 5-year survival of patients with operable advanced laryngeal cancer included in the study was 86.14% and disease-specific survival 86.51%. Lower overall and the disease-specific survival was associated with age, higher histological tumor grade and more extensive neck dissections. Conclusion. Primary total laryngectomy results in higher survival outcomes in cases of transglottic T3 and T4a laryngeal tumors. Patients should be informed of the likely increased mortality risks tied to the choice of surgical resection and treatment modality before their decision. © 2020 Inst. Sci. inf., Univ. Defence in Belgrade. All rights reserved.
