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Current challenges in Wilms' tumor management
Lyndon M Gommersall1, Manit Arya, Imran Mushtaq
1Great Ormond Street Hospital, London, UK.
Abstract:
Wilms' tumor is a renal cancer that predominantly affects children during the first 2 years of life. The continuing success of clinical trials in Wilms' tumor patients over the past 30 years has led to an overall survival of 85%, and treatment-related morbidity has been reduced. Less-aggressive chemotherapeutic regimes are available for patients with validated good prognostic factors, such as low stage and favorable histology. It is becoming increasingly apparent that treatment can be optimized through stratification of patients according to tumor stage and histology. Established treatments for Wilms' tumor include perioperative vincristine and actinomycin, with or without doxorubicin or radiotherapy. Relapsed patients have the option of salvage chemotherapy with ifosfamide, carboplatin and etoposide, as well as high-dose chemotherapy regimes and autologous hemopoietic stem-cell rescue. Further research is required to refine these regimes and identify further the role of additional prognostic factors in this childhood disease. In this article we discuss the most-debated issues and advances that have been made in the management of Wilms' tumor.
Insights
Wilms tumor, a childhood kidney cancer, now has an 85% survival rate due to successful clinical trials. Treatment is optimized by stratifying patients based on tumor stage and histology, reducing morbidity.
Area of Science:
- Pediatric Oncology
- Nephrology
- Cancer Research
Background:
- Wilms tumor is a common pediatric renal cancer affecting children under two.
- Recent clinical trials have improved survival rates to 85% and reduced treatment-related morbidity.
- Less-intensive chemotherapy regimens are now available for patients with favorable prognostic factors.
Purpose of the Study:
- To discuss current management strategies for Wilms tumor.
- To highlight advances in treating this childhood kidney cancer.
- To explore the role of prognostic factors in optimizing treatment.
Main Methods:
- Review of established and salvage chemotherapy regimens.
- Discussion of treatment stratification based on tumor stage and histology.
- Analysis of treatment-related morbidity and survival outcomes.
Main Results:
- Overall survival for Wilms tumor patients has reached 85%.
- Treatment-related morbidity has been significantly reduced.
- Stratification by stage and histology allows for optimized, less-aggressive chemotherapy.
Conclusions:
- Wilms tumor management has advanced significantly, improving survival and reducing morbidity.
- Patient stratification based on prognostic factors is key to optimizing treatment.
- Further research is needed to refine current regimens and identify new prognostic factors.
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