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Age is not a prognostic factor in children with Wilms tumor beyond stage I in Africa
1Department of Paediatric Surgery, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, and Inkosi Albert Luthuli Central Hospital, Durban, South Africa.
Insights
Wilms tumor prognosis in older children (>8 years) did not significantly differ from younger groups, despite initial survival advantages in younger patients with stage I favorable histology. Age did not impact outcomes in advanced stages.
Area of Science:
- Pediatric Oncology
- Cancer Research
- Clinical Studies
Background:
- Favorable histology (FH) Wilms tumor in patients under 4 years is associated with a survival advantage.
- Children over 10 years with Wilms tumor often present with diffuse anaplasia, indicating a poorer prognosis.
Purpose of the Study:
- To investigate if older patients (>8 years) with advanced stage Wilms tumors (II-V) experience a poorer prognosis compared to younger children (<8 or <4 years).
Main Methods:
- A case-control study involving 19 patients over 8 years old with Wilms tumor (stages II-V) matched with two controls each (ages 0-3 and 4-7 years).
- All patients received neo-adjuvant chemotherapy and supportive care, with treatment tailored post-surgery based on stage and histology.
- Overall Survival (OS) and Event-Free Survival (EFS) at 5 years were compared across age groups.
Main Results:
- The study included 19 patients in each age group (over 8, 4-7, and 0-3 years), with tumor stages ranging from II to V.
- Overall survival was 80.8% and EFS was 79.2% for the entire cohort.
- No statistically significant differences in outcomes were observed between the different age groups.
Conclusions:
- The survival advantage seen in younger children (<4 years) with stage I FH Wilms tumor was not evident in higher stages.
- While age did not significantly impact prognosis, a trend towards better outcomes was noted in the youngest group (<4 years).
Background:
Patients under age 4 with stage I favorable histology (FH) Wilms tumor have a reported survival advantage. Among children above 10 years, a poorer prognosis has been associated with a higher prevalence of diffuse anaplasia.
Purpose:
To determine if, in our practice, patients with Wilms tumors >8 years of age (stage II-V) have a poorer prognosis than those aged <8 years or <4 years.
Procedure:
Case-control study of 19 patients >8 years with Wilms tumor stages II-V who were identified from a cohort of 192 new patients (2002-2012). For each patient two controls were chosen matched for stage and histology, one 0-3 years and one 4-7 years. Neo-adjuvant chemotherapy was offered to all, combined with intensive supportive care. Postoperative treatment was determined by local stage and histology. OS and EFS at 5 years for the different age groups were compared.
Results:
Each age group contained 19 patients, of whom 6 had stage II tumors, 3 stage III, 8 stage IV, and 2 stage V. Histology was intermediate risk (IR) in 17 and high risk (HR) in 2. OS at 5 years was 80.8% and EFS was 79.2% for the whole group. No significant difference in outcome could be shown between age groups. Loss to follow up was 6/57 (11%).
Conclusions:
The survival advantage of young age (<4 years) associated with stage I FH could not be demonstrated in higher stages. Age had no significant impact on prognosis although a trend to better outcome was seen in children <4 years.
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