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      Factors Associated with Outcomes at 1 Year in Paediatric Post-nephrectomy Patients for Nephroblastoma at the University Teaching Hospital and Cancer Diseases Hospital in Lusaka, Zambia

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          Abstract

          Background:

          Nephroblastoma is the most common primary malignant renal tumour of childhood. The survival rates in high-income countries are approximately 90%. However, low-income countries have low survival rates of 20%–50%. This study assessed factors associated with treatment outcomes of children post-nephrectomy for nephroblastoma at the University Teaching Hospital and Cancer Diseases Hospital in Lusaka, Zambia.

          Materials and Methods:

          A retrospective observational cohort study was conducted, where all children diagnosed with unilateral Wilms tumour below the age of 16 years who had nephrectomy from July 2016 to June 2019 were enrolled. Sociodemographic, clinical characteristics and treatment outcomes were noted. All data were coded and stored in a tabular format using Microsoft Excel. Statistical software STATA version 13 was used for analysis.

          Results:

          Thirty patients were enrolled. The male-to-female ratio was 1:1. The 1-year event-free survival was 46.7%. Treatment abandonment accounted for 36.6% of the participants. 16.7% of the patients had disease progression. No patient had a relapse or died during the 1-year follow-up period. 66.7% had advanced disease stages III and IV. Advancement in age (above 4.3 years), living in a rural environment more than 100 km away from Lusaka and advanced disease stage were all associated with a poor outcome.

          Conclusions:

          Factors associated with a poor outcome in this study were advanced age and late presentation.

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          Most cited references18

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          Abandonment of treatment for childhood cancer: position statement of a SIOP PODC Working Group.

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            Wilms tumour in Sudan.

            Wilms tumour is one of the commonest childhood solid tumours which has an excellent outlook in the developed world with 5-year overall survival exceeding 90%. There is little information from Sudan regarding Wilms tumour.
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              Management of children with a Wilms tumor in Malawi, sub-Saharan Africa.

              Wilms tumor has a survival rate of 85% to 90% in well-resourced countries. Malawi is a country in Sub-Saharan Africa with very limited resources. We evaluated the outcome of a treatment guideline including preoperative chemotherapy, supportive care, and strategies to enable parents to complete treatment. Between 2006 and 2011, 95 patients were initially diagnosed with a Wilms tumor; 11 were later excluded due to misdiagnosis. In 31% of patients, metastases were detected at presentation. Treatment outcomes in 8 patients with bilateral tumors and 3 patients who were referred after nephrectomy are analyzed separately. Treatment failed in 51% of 73 remaining patients. Reasons for failure were: 1) incomplete treatment (7%); 2) treatment-related deaths (15%); and 3) disease-related deaths (28%) with 11% unresectable tumors or metastases after preoperative chemotherapy and 17% relapse of disease. Projected survival is 46%. Challenges remain to improve survival for children with Wilms tumor in Malawi. Earlier diagnosis would reduce disease-related deaths as numbers of unresectable disease and relapse are high. Effective strategies, including social support, to enable parents to complete treatment need to be continued. Improved supportive care and nutritional support and possibly less intense preoperative chemotherapy are needed to reduce treatment-related deaths.
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                Author and article information

                Journal
                Afr J Paediatr Surg
                Afr J Paediatr Surg
                AJPS
                Afr J Paediatr Surg
                African Journal of Paediatric Surgery: AJPS
                Wolters Kluwer - Medknow (India )
                0189-6725
                0974-5998
                Jul-Sep 2024
                09 August 2024
                : 21
                : 3
                : 172-177
                Affiliations
                [1]Department of Surgery, University Teaching Hospitals, Lusaka, Zambia
                [1 ]Department of Surgery, Levy Mwanawasa Hospital, Lusaka, Zambia
                [2 ]Department of Epidemiology and Biostatistics, University of Zambia, Lusaka, Zambia
                Author notes
                Address for correspondence: Dr. Moonde Zachias Muulu, University Teaching Hospitals, P/Bag RW1X, Lusaka, Zambia. E-mail: moondezmuulu@ 123456gmail.com
                Article
                AJPS-21-172
                10.4103/ajps.ajps_180_21
                11379335
                39162751
                d2e58725-90af-4d2b-bced-c8abac9f1c9f
                Copyright: © 2024 African Journal of Paediatric Surgery

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : 31 December 2021
                : 08 March 2022
                : 20 July 2023
                Categories
                Original Article

                disease progression,nephrectomy,nephroblastoma,relapse,treatment abandonment

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