Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/77067
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dc.contributor.authorThara Tunthanathipen_US
dc.contributor.authorSanguansin Ratanalerten_US
dc.contributor.authorSakchai Sae-Hengen_US
dc.contributor.authorThakul Oearsakulen_US
dc.contributor.authorIttichai Sakarunchaien_US
dc.contributor.authorAnukoon Kaewborisutsakulen_US
dc.contributor.authorThirachit Chotsampancharoenen_US
dc.contributor.authorUtcharee Intusomaen_US
dc.contributor.authorAmnat Kitkhuandeeen_US
dc.contributor.authorTanat Vaniyapongen_US
dc.date.accessioned2022-10-16T07:22:17Z-
dc.date.available2022-10-16T07:22:17Z-
dc.date.issued2021-07-01en_US
dc.identifier.issn19984138en_US
dc.identifier.issn09731482en_US
dc.identifier.other2-s2.0-85115728748en_US
dc.identifier.other10.4103/jcrt.JCRT_233_19en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85115728748&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77067-
dc.description.abstractBackground: Genomic-based tools have been used to predict poor prognosis high-grade glioma (HGG). As genetic technologies are not generally available in countries with limited resources, clinical parameters may be still necessary to use in predicting the prognosis of the disease. This study aimed to identify prognostic factors associated with survival of patients with HGG. We also proposed a validated nomogram using clinical parameters to predict the survival of patients with HGG. Methods: A multicenter retrospective study was conducted in patients who were diagnosed with anaplastic astrocytoma (WHO III) or glioblastoma (WHO IV). Collected data included clinical characteristics, neuroimaging findings, treatment, and outcomes. Prognostic factor analysis was conducted using Cox proportional hazard regression analysis. Then, we used the significant prognostic factors to develop a nomogram. A split validation of nomogram was performed. Twenty percent of the dataset was used to test the performance of the developed nomogram. Results: Data from 171 patients with HGG were analyzed. Overall median survival was 12 months (interquartile range: 5). Significant independent predictors included frontal HGG (hazard ratio [HR]: 0.62; 95% confidence interval [CI]: 0.40–0.60), cerebellar HGG (HR: 4.67; 95% CI: 0.93–23.5), (HR: 1.55; 95% CI: 1.03–2.32; reference = total resection), and postoperative radiotherapy (HR: 0.18; 95% CI: 0.10–0.32). The proposed nomogram was validated using nomogram’s predicted 1-year mortality rate. Sensitivity, specificity, positive predictive value, negative predictive value, accuracy, and area under the curve of our nomogram were 1.0, 0.50, 0.45, 1.0, 0.64, and 0.75, respectively. Conclusion: We developed a nomogram for individually predicting the prognosis of HGG. This nomogram had acceptable performances with high sensitivity for predicting 1-year mortality.en_US
dc.subjectMedicineen_US
dc.titlePrognostic factors and clinical nomogram predicting survival in high-grade gliomaen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Cancer Research and Therapeuticsen_US
article.volume17en_US
article.stream.affiliationsSchool of Medicine, Mae Fah Luang Universityen_US
article.stream.affiliationsFaculty of Medicine, Khon Kaen Universityen_US
article.stream.affiliationsFaculty of Medicine, Prince of Songkia Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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