Underlying undiagnosed inherited marrow failure syndromes among children with cancer

Fahad Alabbas1,2, Sheila Weitzman2, Ronald Grant2

  • 1Marrow Failure and Myelodysplasia Program, Division of Haematology and Oncology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Pediatric Blood & Cancer
|September 1, 2016
PubMed

Insights

A small percentage of pediatric cancer patients may have inherited bone marrow failure syndromes (IBMFS). Further research is needed to confirm the prevalence of IBMFS in children with cancer.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Genetics

Background:

  • Inherited bone marrow failure syndromes (IBMFS) are rare genetic disorders.
  • Early diagnosis of IBMFS is crucial for appropriate management and genetic counseling.
  • The co-occurrence of pediatric cancer and IBMFS requires further investigation.

Purpose of the Study:

  • To determine the prevalence of underlying inherited bone marrow failure syndromes (IBMFS) in pediatric cancer patients.
  • To identify clinical and laboratory findings suggestive of IBMFS in this population.

Main Methods:

  • Retrospective review of medical records of newly diagnosed pediatric cancer patients.
  • Analysis of clinical, laboratory, and treatment-related findings.
  • Inclusion criteria: patients diagnosed between June 2009 and May 2010.

Main Results:

  • Five out of 276 (1.8%) pediatric cancer patients exhibited two or more findings suggestive of IBMFS.
  • The study identified specific indicators within the reviewed data.

Conclusions:

  • A subset of pediatric cancer patients presents with features warranting investigation for underlying IBMFS.
  • Prospective studies are recommended to accurately establish the prevalence of IBMFS in pediatric cancer patients.

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