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Published on: February 8, 2020
Clinicohistological characteristics of renal cell carcinoma in children: A multicentre study
Jeong Ho Kim1, Seong Il Seo2, Cheryn Song3
1Department of Urology, Dongnam Institute of Radiological & Medical Sciences Cancer center, Busan, Korea;
Insights
Renal cell carcinoma (RCC) in children is rare and presents differently than in adults, often with more advanced stages. However, survival outcomes for pediatric and adult RCC patients were similar in this study.
Area of Science:
- Urology
- Oncology
- Pediatric Nephrology
Background:
- Renal cell carcinoma (RCC) is uncommon in children.
- Clinicopathological differences between pediatric and adult RCC are not well-defined.
Purpose of the Study:
- To compare clinicopathological characteristics and survival outcomes of pediatric versus adult RCC patients.
- To identify distinct features of RCC in different age groups.
Main Methods:
- Retrospective multicenter study of RCC patients who underwent nephrectomy (1988-2014).
- Patients categorized into pediatric (≤18 years) and adult (≥40 years) groups.
- Comparison of clinical, pathological variables, and survival analysis.
Main Results:
- Pediatric patients presented more frequently with symptoms and advanced-stage tumors.
- Histologically, pediatric RCC showed more papillary and unclassified types, and fewer clear cell carcinomas.
- Five-year cancer-specific survival rates were comparable (85% pediatric vs. 87.4% adult).
Conclusions:
- Pediatric RCC exhibits distinct clinicopathological features compared to adult RCC.
- Despite differences in presentation and histology, survival outcomes are similar between pediatric and adult patients.
- Further research is needed due to the retrospective nature and limited pediatric cases.
Introduction:
In this retrospective multicentre study, we compared the clinicohistological characteristics of renal cell carcinoma (RCC) between pediatric and adult patients.
Methods:
Data for patients who underwent radical or partial nephrectomy for RCC between 1988 and 2014 at multiple institutions were collected. Patients were divided into 2 groups according to age at diagnosis: pediatric patients (age ≤18 years) and adult patients (age ≥40 years). The groups were compared for clinical and pathologic variables, and survival analysis was performed.
Results:
The median follow-up period was 64 (range: 30-91) months for pediatric patients versus 44 (range: 19-59) months for adult patients (p = 0.026). Pediatric patients were mostly female (p = 0.003), had symptoms at presentation (p < 0.001), and had a high-stage tumour (p = 0.014) than adult patients. Among the symptomatic patients, gross hematuria was the most common symptom. The median tumour size was not different between groups. Regarding histologic types, pediatric patients had more papillary tumours (p < 0.001), more unclassified tumours (p < 0.001), and fewer clear cell carcinomas (p < 0.001). Five-year cancer-specific survival rates were 85% and 87.4% in pediatric and adult patients, respectively (log rank p = 0.901). Recurrence-free survival was better in adult patients, although this did not reach statistical significance (log rank p = 0.272). This study has several limitations, including its retrospective nature and the relatively small number of pediatric RCC cases.
Conclusion:
RCC in children is rare and is characterized by features that differ from those in adult RCC. Prognosis did not differ between groups.
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