Invasive pneumococcal disease in children with cancer: Incidence density, risk factors and isolated serotypes

Pedro Mendes Lages1, Fabianne Carlesse1, Bruno Cruz Boettger2

  • 1Universidade Federal de São Paulo, Departamento de Pediatria, São Paulo, SP, Brazil.

Insights

Invasive pneumococcal disease (IPD) remains a significant threat to children with cancer, with severe neutropenia as a key risk factor. Increased vaccination coverage in the general population may be crucial to protect this vulnerable group.

Area of Science:

  • Pediatric Oncology
  • Infectious Diseases
  • Epidemiology

Background:

  • Pediatric oncology patients (POP) face heightened infection risks due to compromised immunity.
  • Invasive pneumococcal disease (IPD) is a critical cause of severe infections and mortality in POP.
  • This study investigated IPD incidence and risk factors in Brazilian pediatric cancer patients.

Purpose of the Study:

  • To determine the incidence rate of IPD in pediatric oncology patients in Brazil.
  • To identify risk factors associated with IPD in this high-risk population.
  • To evaluate the impact of pneumococcal vaccination on IPD rates in POP.

Main Methods:

  • Retrospective case-control study design.
  • Inclusion of all IPD cases in children with cancer from 2005-2016.
  • Matching cases with controls for age, year of IPD, and disease type; incidence density calculated per 100,000 patients-year.

Main Results:

  • 51 IPD episodes identified in 49 patients; 7.8% mortality rate.
  • IPD incidence density was 311.21 per 100,000 patients-year, significantly exceeding the general pediatric rate.
  • Severe neutropenia was the sole identified risk factor for IPD.

Conclusions:

  • Despite the introduction of the 10-valent pneumococcal vaccine, IPD incidence in the studied cohort did not decrease.
  • A higher pneumococcal vaccination coverage rate in the general pediatric population is suggested as necessary.
  • Protecting vulnerable pediatric oncology patients from IPD requires broader community immunity.
Abstract

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