Wilms′ tumour: Determinants of prognosis in an African setting

Background: The few studies available in the literature on Wilms′ tumour (WT) from sub-Saharan Africa have reported a dismal outcome for children with the tumour. This study evaluated the risk factors that have been correlated with outcome in the literature and compare these with outcome among our p...

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Main Authors: Akinfenwa Taoheed Atanda, Lofty-John Chuhwuemeka Anyanwu, Oladoyin Jareenat Atanda, Aminu Mohammad Mohammad, Lawal Barau Abdullahi, Aliyu Umar Farinyaro
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:African Journal of Paediatric Surgery
Subjects:
p53
Online Access:http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2015;volume=12;issue=3;spage=171;epage=176;aulast=Atanda
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spelling doaj-d7b7eb5791cb4c3bb8f97f64736083802020-11-25T01:27:40ZengWolters Kluwer Medknow PublicationsAfrican Journal of Paediatric Surgery0189-67250974-59982015-01-0112317117610.4103/0189-6725.170185Wilms′ tumour: Determinants of prognosis in an African settingAkinfenwa Taoheed AtandaLofty-John Chuhwuemeka AnyanwuOladoyin Jareenat AtandaAminu Mohammad MohammadLawal Barau AbdullahiAliyu Umar FarinyaroBackground: The few studies available in the literature on Wilms′ tumour (WT) from sub-Saharan Africa have reported a dismal outcome for children with the tumour. This study evaluated the risk factors that have been correlated with outcome in the literature and compare these with outcome among our patients. Materials and Methods: Cases of histologically confirmed WT between 2009 and 2013 in a tertiary hospital in Northwestern Nigeria were evaluated for gender, age, laterality, symptoms, duration before presentation, stage at presentation, histologic subtype and p53 mutation. These were then correlated with outcome. Results: Totally, 30 cases of WT were diagnosed with mean age of 4.8 ± 1.9 years; and male:female ratio of 2:1. No statistically significant relationship with outcome was found for gender (P = 0.138) or histologic subtype (P = 0.671). The most significant variables which positively influenced the outcome were presentation at earlier stages (P = 0.007) and completion of therapy (P = 0.0007). p53 mutation was seen in 3 (16.7%) of 18 cases and was not associated with a poor outcome (P = 0.089). However, 2 of the 3 cases presented in Stage IV and none of them survived the 1 st year. Conclusion: This study shows that even though p53 mutation was associated with a more aggressive phenotype, the most significant determinants of a good outcome among patients in a developing country like ours is non-blastemal dominant histologic subtype, early stage at presentation and completion of therapy.http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2015;volume=12;issue=3;spage=171;epage=176;aulast=AtandaBlastemaoutcomep53Wilms′ tumour
collection DOAJ
language English
format Article
sources DOAJ
author Akinfenwa Taoheed Atanda
Lofty-John Chuhwuemeka Anyanwu
Oladoyin Jareenat Atanda
Aminu Mohammad Mohammad
Lawal Barau Abdullahi
Aliyu Umar Farinyaro
spellingShingle Akinfenwa Taoheed Atanda
Lofty-John Chuhwuemeka Anyanwu
Oladoyin Jareenat Atanda
Aminu Mohammad Mohammad
Lawal Barau Abdullahi
Aliyu Umar Farinyaro
Wilms′ tumour: Determinants of prognosis in an African setting
African Journal of Paediatric Surgery
Blastema
outcome
p53
Wilms′ tumour
author_facet Akinfenwa Taoheed Atanda
Lofty-John Chuhwuemeka Anyanwu
Oladoyin Jareenat Atanda
Aminu Mohammad Mohammad
Lawal Barau Abdullahi
Aliyu Umar Farinyaro
author_sort Akinfenwa Taoheed Atanda
title Wilms′ tumour: Determinants of prognosis in an African setting
title_short Wilms′ tumour: Determinants of prognosis in an African setting
title_full Wilms′ tumour: Determinants of prognosis in an African setting
title_fullStr Wilms′ tumour: Determinants of prognosis in an African setting
title_full_unstemmed Wilms′ tumour: Determinants of prognosis in an African setting
title_sort wilms′ tumour: determinants of prognosis in an african setting
publisher Wolters Kluwer Medknow Publications
series African Journal of Paediatric Surgery
issn 0189-6725
0974-5998
publishDate 2015-01-01
description Background: The few studies available in the literature on Wilms′ tumour (WT) from sub-Saharan Africa have reported a dismal outcome for children with the tumour. This study evaluated the risk factors that have been correlated with outcome in the literature and compare these with outcome among our patients. Materials and Methods: Cases of histologically confirmed WT between 2009 and 2013 in a tertiary hospital in Northwestern Nigeria were evaluated for gender, age, laterality, symptoms, duration before presentation, stage at presentation, histologic subtype and p53 mutation. These were then correlated with outcome. Results: Totally, 30 cases of WT were diagnosed with mean age of 4.8 ± 1.9 years; and male:female ratio of 2:1. No statistically significant relationship with outcome was found for gender (P = 0.138) or histologic subtype (P = 0.671). The most significant variables which positively influenced the outcome were presentation at earlier stages (P = 0.007) and completion of therapy (P = 0.0007). p53 mutation was seen in 3 (16.7%) of 18 cases and was not associated with a poor outcome (P = 0.089). However, 2 of the 3 cases presented in Stage IV and none of them survived the 1 st year. Conclusion: This study shows that even though p53 mutation was associated with a more aggressive phenotype, the most significant determinants of a good outcome among patients in a developing country like ours is non-blastemal dominant histologic subtype, early stage at presentation and completion of therapy.
topic Blastema
outcome
p53
Wilms′ tumour
url http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2015;volume=12;issue=3;spage=171;epage=176;aulast=Atanda
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