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One year overall survival of wilms tumor cases and its predictors, among children diagnosed at a teaching hospital in South Western Uganda: a retrospective cohort study.
Ekuk, Eddymond; Odongo, Charles Newton; Tibaijuka, Leevan; Oyania, Felix; Egesa, Walufu Ivan; Bongomin, Felix; Atwiine, Raymond; Acan, Moses; Situma, Martin.
Afiliação
  • Ekuk E; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda. eddiemakori@yahoo.com.
  • Odongo CN; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
  • Tibaijuka L; Department of Anatomy, Faculty of Medicine Soroti University, Soroti, Uganda.
  • Oyania F; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
  • Egesa WI; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
  • Bongomin F; Department of Pediatrics, Faculty of Clinical Medicine and Dentistry, Kampala International, Kampala, Uganda.
  • Atwiine R; Department of Microbiology, Mycology, and Immunology, Internal Medicine Gulu University, Gulu, Uganda.
  • Acan M; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
  • Situma M; Department of Surgery, Mbarara University of Science and Technology, Faculty of Medicine, Mbarara, Uganda.
BMC Cancer ; 23(1): 196, 2023 Mar 02.
Article em En | MEDLINE | ID: mdl-36864435
BACKGROUND: Wilms tumor (WT) is the second most common solid tumor in Africa with both low overall survival (OS) and event-free survival (EFS) rates. However, no known factors are predicting this poor overall survival. OBJECTIVE: The study was to determine the one-year overall survival of WT cases and its predictors among children diagnosed in the pediatric oncology and surgical units of Mbarara regional referral hospital (MRRH), western Uganda. METHODOLOGY: Children's treatment charts and files diagnosed and managed for WT were retrospectively followed up for the period between January 2017 to January 2021. Charts of children with histologically confirmed diagnoses were reviewed for demographics, clinical and histological characteristics, as well as treatment modalities. RESULTS: One-year overall survival was found to be 59.3% (95% CI: 40.7-73.3), with tumor size greater than 15 cm (p 0.021) and unfavorable WT type (p 0.012) being the predominant predictors. CONCLUSION: Overall survival (OS) of WT at MRRH was found to be 59.3%, and predictive factors noted were unfavorable histology and tumor size greater than 115 cm.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Segunda Neoplasia Primária / Tumor de Wilms / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans País/Região como assunto: Africa Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Uganda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Segunda Neoplasia Primária / Tumor de Wilms / Neoplasias Renais Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans País/Região como assunto: Africa Idioma: En Revista: BMC Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Uganda