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Wilms Tumor in India: A Systematic Review
Shyam Srinivasan1, Subramaniam Ramanathan2, Maya Prasad1
1Department of Pediatric Oncology, Homi Bhabha National Institute, Tata Memorial Hospital, Mumbai, Maharashtra, India.
South Asian Journal of Cancer
|November 16, 2023
Summary
Childhood Wilms tumor (WT) survival in India is modest, with many patients presenting with advanced disease. Improved outcomes may be achieved through collaborative strategies for early expert care access and social support to enhance treatment compliance.
Area of Science:
- Pediatric Oncology
- Nephroblastoma Research
- Cancer Epidemiology in India
Background:
- Childhood cancer cure rates in India lag behind upper-middle-income countries.
- Limited data exists on the outcomes of childhood Wilms tumor (WT) in India.
- This review addresses disease trends, treatment, and outcomes for WT in India.
Purpose of the Study:
- To systematically review and analyze data on childhood Wilms tumor in India.
- To assess disease characteristics, treatment strategies, and survival indicators.
- To identify factors influencing outcomes and propose strategies for improvement.
Main Methods:
- Systematic search of MEDLINE, Google Scholar, and SCOPUS databases.
- Inclusion of International Society of Pediatric Oncology conference abstracts.
- Extraction of data on Wilms tumor (nephroblastoma) from Indian studies.
Main Results:
- 17 studies with 1,170 patients were reviewed; 94% published post-2010.
- 46% of patients presented with advanced stage (III/IV) disease.
- Overall survival ranged from 48-89%; high non-relapse mortality (2.7-8.5%) was observed. Key prognostic factors included tumor volume, metastasis, and unfavorable histology.
Conclusions:
- A significant proportion of Indian children with WT present with advanced disease.
- Current survival rates for WT in India are modest, despite treatment efforts.
- Collaborative strategies focusing on early expert care access and social support are crucial for improving WT survival in India.
