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Treating childhood cancer in Rwanda: the nephroblastoma example

INTRODUCTION: Wilms tumor (WT) or nephroblastoma is the commonest childhood cancer in Rwanda. Nephroblastoma is regarded as one of the successes of pediatric oncology with long-term survival approaching 90%. The Objectives to evaluate the feasibilityof treating childhood cancer using the nephroblast...

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Autores principales: Kanyamuhunga, Aimable, Tuyisenge, Lisine, Stefan, Daniela Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646289/
https://www.ncbi.nlm.nih.gov/pubmed/26600901
http://dx.doi.org/10.11604/pamj.2015.21.326.5912
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author Kanyamuhunga, Aimable
Tuyisenge, Lisine
Stefan, Daniela Cristina
author_facet Kanyamuhunga, Aimable
Tuyisenge, Lisine
Stefan, Daniela Cristina
author_sort Kanyamuhunga, Aimable
collection PubMed
description INTRODUCTION: Wilms tumor (WT) or nephroblastoma is the commonest childhood cancer in Rwanda. Nephroblastoma is regarded as one of the successes of pediatric oncology with long-term survival approaching 90%. The Objectives to evaluate the feasibilityof treating childhood cancer using the nephroblastoma example and to calculate its cost of treatment in Rwanda. METHODS: Prospective study over a 2 year period: 01 Jan 2010- 31 December 2011. A questionnaire was completed by all participants in the study and the following variables were collected at Kigali University Teaching Hospital: age at diagnosis, gender, transport cost, cost of investigations, staging, treatment and outcome, cost of hospitalization, type of medical, surgical, radiological interventions and their costs, number of admissions per patient and factors related to non compliance to treatment. All patients had a confirmed diagnosis on histopathology examination. The cost for treatment was calculated for early and late stage and was expressed in USA dollars. Analysis was done with SPSS 16.0. RESULTS: There were 25 patients diagnosed and treated for WT during the study period. Almost half of the patients 14/25 (56%) had advanced disease, seven children (28%) had stage IV, seven children stage III, six patients (24%) with stage II, while the remaining five (20%) had stage I with high risk tumor. The direct cost of management ranged from1,831.2 USD for early disease to 2,418.7 USD for advanced disease. The cost of transport, investigations and drugs were recorded as main contributing factors to the feasibility and cost of the treatment in 80% of the responses, followed by late presentation (56%) and poor compliance to treatment. CONCLUSION: Most challenges are related to unaffordable treatment and late presentation. The management of WT is feasible in Rwandan setting but efforts should be made in order to improve awareness of childhood cancer, early diagnosis and access to care. The government of Rwanda is committed to improve cancer care in the country and organized the first pediatric international oncology conference in Kigali, in March 2012 to develop National protocols for the top five most common cancers in children.
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spelling pubmed-46462892015-11-23 Treating childhood cancer in Rwanda: the nephroblastoma example Kanyamuhunga, Aimable Tuyisenge, Lisine Stefan, Daniela Cristina Pan Afr Med J Research INTRODUCTION: Wilms tumor (WT) or nephroblastoma is the commonest childhood cancer in Rwanda. Nephroblastoma is regarded as one of the successes of pediatric oncology with long-term survival approaching 90%. The Objectives to evaluate the feasibilityof treating childhood cancer using the nephroblastoma example and to calculate its cost of treatment in Rwanda. METHODS: Prospective study over a 2 year period: 01 Jan 2010- 31 December 2011. A questionnaire was completed by all participants in the study and the following variables were collected at Kigali University Teaching Hospital: age at diagnosis, gender, transport cost, cost of investigations, staging, treatment and outcome, cost of hospitalization, type of medical, surgical, radiological interventions and their costs, number of admissions per patient and factors related to non compliance to treatment. All patients had a confirmed diagnosis on histopathology examination. The cost for treatment was calculated for early and late stage and was expressed in USA dollars. Analysis was done with SPSS 16.0. RESULTS: There were 25 patients diagnosed and treated for WT during the study period. Almost half of the patients 14/25 (56%) had advanced disease, seven children (28%) had stage IV, seven children stage III, six patients (24%) with stage II, while the remaining five (20%) had stage I with high risk tumor. The direct cost of management ranged from1,831.2 USD for early disease to 2,418.7 USD for advanced disease. The cost of transport, investigations and drugs were recorded as main contributing factors to the feasibility and cost of the treatment in 80% of the responses, followed by late presentation (56%) and poor compliance to treatment. CONCLUSION: Most challenges are related to unaffordable treatment and late presentation. The management of WT is feasible in Rwandan setting but efforts should be made in order to improve awareness of childhood cancer, early diagnosis and access to care. The government of Rwanda is committed to improve cancer care in the country and organized the first pediatric international oncology conference in Kigali, in March 2012 to develop National protocols for the top five most common cancers in children. The African Field Epidemiology Network 2015-08-31 /pmc/articles/PMC4646289/ /pubmed/26600901 http://dx.doi.org/10.11604/pamj.2015.21.326.5912 Text en © Aimable Kanyamuhunga et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kanyamuhunga, Aimable
Tuyisenge, Lisine
Stefan, Daniela Cristina
Treating childhood cancer in Rwanda: the nephroblastoma example
title Treating childhood cancer in Rwanda: the nephroblastoma example
title_full Treating childhood cancer in Rwanda: the nephroblastoma example
title_fullStr Treating childhood cancer in Rwanda: the nephroblastoma example
title_full_unstemmed Treating childhood cancer in Rwanda: the nephroblastoma example
title_short Treating childhood cancer in Rwanda: the nephroblastoma example
title_sort treating childhood cancer in rwanda: the nephroblastoma example
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646289/
https://www.ncbi.nlm.nih.gov/pubmed/26600901
http://dx.doi.org/10.11604/pamj.2015.21.326.5912
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