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Published on: June 12, 2017
Survival of children with a Wilms tumor in Blantyre, Malawi
Trijn Israels1, Dalida Pidini2, Eric Borgstein3
1a Department of Paediatric Oncology and Academy Outreach , Princess Maxima Centre for Pediatric Oncology , Utrecht , The Netherlands.
Insights
Survival rates for Wilms tumor (WT) in Malawi remain low despite adapted treatment. Long-term follow-up is crucial for assessing outcomes and intervention impact in pediatric cancer care.
Area of Science:
- Pediatric Oncology
- Global Health
Background:
- Wilms tumor (WT) survival exceeds 90% in high-income nations, contrasting sharply with lower rates in sub-Saharan Africa.
- Long-term outcomes for WT in sub-Saharan Africa are poorly understood due to follow-up challenges.
Purpose of the Study:
- To evaluate the outcomes of an adapted Wilms tumor treatment guideline implemented in Blantyre, Malawi.
- To assess event-free survival and identify causes of treatment failure in children with WT.
Main Methods:
- An adapted WT treatment guideline, including preoperative chemotherapy and enhanced supportive care, was introduced in 2006.
- 73 children with unilateral WT were treated between 2006-2011 with a focus on consistent follow-up, including home visits.
- Median follow-up was 5 years, with event-free survival assessed at 2 and 5 years.
Main Results:
- Two and five-year event-free survival rates were 46% and 42%, respectively.
- Treatment failures included 7% abandonment, 15% death during treatment, and 30% disease-related deaths (persistent disease/relapse).
Conclusions:
- The adapted WT treatment guideline showed limited initial success in improving survival rates in Malawi.
- Challenges in long-term follow-up hinder accurate assessment of pediatric cancer outcomes and intervention effectiveness.
- Strategies to improve treatment completion and long-term monitoring are essential for enhancing Wilms tumor care in low-resource settings.
Abstract:
Wilms tumor (WT) has a survival rate above 90% in high income countries. Reported survival rates in sub-Saharan Africa are much lower and long-term outcome is not well known as follow-up is challenging. In Blantyre, Malawi, an adapted WT treatment guideline with preoperative chemotherapy, supportive care, and strategies to enable children and parents to complete treatment was introduced in 2006. Between 2006 and 2011, 73 children with a unilateral WT were treated. Follow-up, including home visits when needed, was done. Median follow-up time is 5 years (range 14-95 months). Two and five-year event free survivals are 46 and 42%. Causes of treatment failure are: 7% (5/73) abandonment of treatment, 15% (11/73) death during treatment and 30% (22/73) disease-related deaths (persistent disease and relapse). Long-term follow-up is challenging but necessary to be able to assess outcome and the true impact of interventions.
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