Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes

  • Jane E. Churpek
  • , Rachelle Lorenz
  • , Siya Nedumgottil
  • , Kenan Onel
  • , Olufunmilayo I. Olopade
  • , April Sorrell
  • , Carolyn J. Owen
  • , Alison A. Bertuch
  • , Lucy A. Godley

Research output: Contribution to journalReview articlepeer-review

85 Scopus citations

Abstract

As with most genetic cancer predisposition syndromes, inherited susceptibility to myelodysplastic syndrome (MDS) and acute leukemia (AL) is likely to be more common than previously appreciated. As next-generation sequencing technologies become integrated into clinical practice, we anticipate that the number of cases of familial MDS/AL identified will increase. Although the existence of syndromes predisposing to MDS/AL has been known for some time, clinical guidelines for the screening and management of suspected or confirmed cases do not exist. Based on our collective experience caring for families with these syndromes, we propose recommendations for genetic counseling, testing, and clinical management. We welcome discussion about these proposals and hope that they will catalyze an ongoing dialog leading to optimal medical and psychosocial care for these patients.

Original languageEnglish
Pages (from-to)28-35
Number of pages8
JournalLeukemia and Lymphoma
Volume54
Issue number1
DOIs
StatePublished - Jan 2013
Externally publishedYes

Keywords

  • CEBPA
  • GATA2
  • Leukemia
  • MDS
  • Predisposition
  • RUNX1

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