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Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy. | LitMetric

AI Article Synopsis

  • * Recent studies have expanded the list of these gene variants, leading to updates on surveillance and intervention strategies for at-risk children, including early hematopoietic stem cell transplantation.
  • * A 2023 expert panel provided new recommendations for monitoring these children, emphasizing personalized approaches based on genetic profiles, including regular check-ups and specialized testing like bone marrow examinations and gene sequencing.

Article Abstract

Children harboring certain germline gene variants have an increased risk of developing myelodysplastic syndrome (MDS) and other hematopoietic malignancies (HM), such as leukemias and lymphomas. Recent studies have identified an expanding number of these predisposition genes, with variants most prevalent in children with MDS but also found in children with other HM. For some hematopoietic malignancy predispositions (HMP), specifically those with a high risk of MDS, early intervention through hematopoietic stem cell transplantation can favorably impact overall survival, providing a rationale for rigorous surveillance. A multidisciplinary panel of experts at the 2023 AACR Childhood Cancer Predisposition Workshop reviewed the latest advances in the field and updated prior 2017 surveillance recommendations for children with HMP. In addition to general guidance for all children with HMP, which includes annual physical examination, education about the signs and symptoms of HM, consultation with experienced providers, and early assessment by a hematopoietic stem cell transplantation specialist, the panel provided specific recommendations for individuals with a higher risk of MDS based on the affected gene. These recommendations include periodic and comprehensive surveillance for individuals with those syndromes associated with higher risk of MDS, including serial bone marrow examinations to monitor for morphologic changes and deep sequencing for somatic changes in genes associated with HM progression. This approach enables close monitoring of disease evolution based on the individual's genetic profile. As more HMP-related genes are discovered and the disorders' natural histories are better defined, these personalized recommendations will serve as a foundation for future guidelines in managing these conditions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11444884PMC
http://dx.doi.org/10.1158/1078-0432.CCR-24-0685DOI Listing

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