Prognosis and treatment of Wilms' tumor at Great Ormond Street Hospital for Sick Children--1960-1972

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Cancer
|October 1, 1975
PubMed

Insights

Wilms' tumor survival rates varied significantly by stage, with advanced stages showing poorer outcomes. Intensive therapy, including multi-drug chemotherapy, is crucial for improving survival in advanced Wilms' tumor cases.

Area of Science:

  • Pediatric Oncology
  • Nephrology

Background:

  • Wilms' tumor is a common pediatric kidney cancer.
  • Treatment strategies and survival rates have evolved over time.

Purpose of the Study:

  • To review treatment outcomes and survival rates for Wilms' tumor in children treated between 1960-1972.
  • To identify prognostic factors and necessary therapeutic interventions for improved patient outcomes.

Main Methods:

  • Retrospective review of 81 children diagnosed with Wilms' tumor.
  • Utilized the National Wilms' Tumor Study group staging system for classification.
  • Analysis of age, sex, treatment, and survival data.

Main Results:

  • Survival rates were 87% (Stage I), 36% (Stage II), 8% (Stage III), and 33% (Stage IV).
  • Locally advanced tumors had worse survival than those with pulmonary metastases and resectable primary tumors.
  • Whole abdominal irradiation is critical for tumors breaching the renal capsule.
  • Single-agent chemotherapy was ineffective for advanced tumors; multi-drug chemotherapy improved disease-free survival.

Conclusions:

  • Wilms' tumor prognosis is heavily stage-dependent.
  • Advanced Wilms' tumor requires intensive therapeutic approaches, including multi-drug chemotherapy, nephrectomy, and whole abdominal irradiation.
  • Current intensive therapies show promise in enhancing disease-free survival for pediatric Wilms' tumor patients.

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