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Published on: February 23, 2014
Invasive pneumococcal disease in children with acute lymphoblastic leukaemia.
Linny Kimly Phuong1,2,3, Amanda Gwee1,2,3,4, Christopher C Blyth5,6,7
1Infection & Immunity Theme Group, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Children with acute lymphoblastic leukaemia (ALL) face a significantly higher risk of invasive pneumococcal disease (IPD) even after pneumococcal conjugate vaccine (PCV) use. Most IPD cases were caused by non-PCV13 serotypes, highlighting the need for better vaccination strategies.
Area of Science:
- Paediatric Oncology
- Infectious Diseases
- Immunology
Background:
- Widespread use of pneumococcal conjugate vaccines (PCVs) has reduced invasive pneumococcal disease (IPD) in the general population.
- Children undergoing cancer treatment, particularly acute lymphoblastic leukaemia (ALL), may have altered immune responses and remain vulnerable to infections.
Purpose of the Study:
- To assess the incidence, serotype distribution, and clinical outcomes of IPD in children with ALL post-PCV implementation.
- To compare IPD rates in children with cancer against the general paediatric population.
Main Methods:
- A multicentre cohort study was conducted across two tertiary paediatric oncology centres in Australia.
- Data on pneumococcal vaccination status, IPD episodes, serotypes, and clinical outcomes were collected for children with cancer, including a subgroup with ALL.
Main Results:
- 29 IPD episodes occurred in 28 children with cancer (19 with ALL).
- The incidence of IPD in children with ALL was 190-360 times higher than in healthy children.
- Most IPD cases (83%) were caused by non-PCV13 serotypes (e.g., 23B), and additional pneumococcal vaccination uptake was low.
Conclusions:
- Children with ALL have a substantially increased risk of IPD despite PCV use, primarily due to non-PCV13 serotypes.
- Low uptake of additional pneumococcal vaccine doses was observed.
- Optimized vaccination and prophylactic strategies are crucial for this vulnerable paediatric oncology population.
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