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Screening for neuroblastoma in North America. 2-year results from the Quebec Project

W G Woods1, M Tuchman, M L Bernstein

  • 1Department of Pediatrics, University of Minnesota Hospital, Minneapolis.

The American Journal of Pediatric Hematology/Oncology
|November 1, 1992
PubMed

Insights

The Quebec Neuroblastoma Screening Project screened over 157,000 infants for neuroblastoma using urinary catecholamine metabolites. This infant screening program identified neuroblastoma in 0.02% of participants, demonstrating its potential for early detection.

Area of Science:

  • Pediatric Oncology
  • Screening Programs
  • Biomarker Detection

Background:

  • Neuroblastoma is a common childhood cancer.
  • Early detection of neuroblastoma can improve patient outcomes.
  • Screening programs are essential for identifying at-risk populations.

Purpose of the Study:

  • To evaluate the effectiveness of mass screening for neuroblastoma in newborns.
  • To assess the clinical and biological aspects of infant neuroblastoma screening.
  • To determine the yield of a two-stage screening protocol using urinary catecholamine metabolites.

Main Methods:

  • Infants born in Quebec were screened for neuroblastoma.
  • Urine-saturated filter paper was used to measure vanillylmandelic acid (VMA) and homovanillic acid (HVA).
  • A two-stage screening process involved initial testing at 3 weeks and 6 months of age.

Main Results:

  • Over 157,000 infants were screened at 3 weeks and over 98,000 at 6 months.
  • 340 infants (0.13%) required further laboratory examination due to elevated VMA/HVA levels.
  • Neuroblastoma was diagnosed in 9 children (0.02%) through the screening program.

Conclusions:

  • Infant screening for neuroblastoma using urinary VMA and HVA is feasible and identifies cases.
  • The screening program demonstrated a low but significant detection rate for neuroblastoma.
  • Further evaluation is needed to optimize screening protocols and assess long-term benefits.

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