The incidence of brainstem primitive neuroectodermal tumors of childhood based on SEER data

Childs Nerv Syst. 2018 Mar;34(3):431-439. doi: 10.1007/s00381-017-3687-4. Epub 2018 Jan 3.

Abstract

Purpose: Incidence of BS primitive neuroectodermal tumors (BS-PNET) in children is not reported to date. Our main objectives were to estimate the incidence and report the outcome of BS-PNET in children.

Methods: Data were collected using the Surveillance Epidemiology and End Results cancer registry.

Results: From 1973 to 2013, we identified 83 pediatric patients (aged 0-21 years). Patients were divided into two age groups (0-3 years and 4-21 years). Median overall survival was 53 months. Patients in the older age group had a significant survival advantage (P < 0.001), as did those who received three modalities of therapy (surgery, chemotherapy, and radiation therapy) (P < 0.001) and patients with gross or subtotal tumor resection (P < 0.001).

Conclusions: This study presents the first estimate of incidence and the largest cohort of pediatric BS-PNETs to date. A high index of suspicion of BS-PNET in similar cases is crucial for diagnosis, treatment, and outcome.

Keywords: Biopsy; Brainstem tumor; Embryonal tumor; Outcome.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Brain Stem Neoplasms / diagnostic imaging*
  • Brain Stem Neoplasms / epidemiology*
  • Brain Stem Neoplasms / therapy
  • Child
  • Child, Preschool
  • Cohort Studies
  • Data Analysis*
  • Female
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Male
  • Neuroectodermal Tumors, Primitive / diagnostic imaging*
  • Neuroectodermal Tumors, Primitive / epidemiology*
  • Neuroectodermal Tumors, Primitive / therapy
  • SEER Program / trends*
  • Young Adult