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Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy.
Maese, Luke D; Wlodarski, Marcin W; Kim, Sun Young; Bertuch, Alison A; Bougeard, Gaelle; Chang, Vivian Y; Godley, Lucy A; Khincha, Payal P; Kuiper, Roland P; Lesmana, Harry; McGee, Rose B; McReynolds, Lisa J; Meade, Julia; Plon, Sharon E; Savage, Sharon A; Scollon, Sarah R; Scott, Hamish S; Walsh, Michael F; Nichols, Kim E; Porter, Christopher C.
Affiliation
  • Maese LD; University of Utah-Huntsman Cancer Institute, Primary Children's Hospital, Salt Lake City, Utah.
  • Wlodarski MW; St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Kim SY; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Bertuch AA; Department of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.
  • Bougeard G; Université de Rouen Normandie, Inserm U1245 and Rouen University Hospital, Rouen, France.
  • Chang VY; University of California Los Angeles, Los Angeles, California.
  • Godley LA; Division of Hematology/Oncology, Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
  • Khincha PP; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Kuiper RP; Princess Máxima Center for Pediatric Oncology and Department of Genetics, Utrecht University Medical Center, Utrecht University, Utrecht, the Netherlands.
  • Lesmana H; Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.
  • McGee RB; St. Jude Children's Research Hospital, Memphis, Tennessee.
  • McReynolds LJ; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Meade J; University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Plon SE; Department of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.
  • Savage SA; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Scollon SR; Department of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.
  • Scott HS; Centre for Cancer Biology, SA Pathology and University of South Australia, Adelaide, South Australia, Australia.
  • Walsh MF; Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.
  • Nichols KE; St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Porter CC; Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia.
Clin Cancer Res ; 30(19): 4286-4295, 2024 Oct 01.
Article in En | MEDLINE | ID: mdl-39078402
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematologic Neoplasms / Genetic Predisposition to Disease Limits: Child / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematologic Neoplasms / Genetic Predisposition to Disease Limits: Child / Humans Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2024 Document type: Article Country of publication: