At what age could screening for familial retinoblastoma be stopped? A register based study 1945-98

Br J Ophthalmol. 2000 Oct;84(10):1170-2. doi: 10.1136/bjo.84.10.1170.

Abstract

Aim: To evaluate until what age children in families with retinoblastoma should be screened.

Methods: A register based cohort (n= 685) study of Dutch retinoblastoma patients (1945-1998). The records of all familial hereditary retinoblastoma patients from 1945 were reviewed and the age at diagnosis and either they were screened from birth determined.

Results: 75 patients had the familial hereditary form of retinoblastoma. The mean age at diagnosis in patients with fundus screening (n=50) from birth on was 4.9 months (median 1.9 months; range 1 day to 48 months). Thus, 4 years was the latest onset of familial retinoblastoma properly evaluated from birth. This mean age was significantly different (p<0.0001) from the mean age at diagnosis in patients without fundus screening (n=25) from birth (mean 17.2 months; median 10.0 months; range 1.5-63.0 months).

Conclusions: Ophthalmological screening of children and sibs at risk for familial hereditary retinoblastoma is recommended until the age of 4 years in order to detect retinoblastoma as early as possible.

MeSH terms

  • Age Factors
  • Child, Preschool
  • Cohort Studies
  • Humans
  • Infant
  • Mass Screening / organization & administration*
  • Neoplastic Syndromes, Hereditary / diagnosis*
  • Netherlands
  • Registries
  • Retinal Neoplasms / diagnosis*
  • Retinal Neoplasms / genetics
  • Retinoblastoma / diagnosis*
  • Retinoblastoma / genetics