Evidence map›Paper›PMID 39078402›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2024

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

Luke D Maese, Marcin W Wlodarski, Sun Young Kim, Alison A Bertuch, Gaelle Bougeard, Vivian Y Chang, Lucy A Godley, Payal P Khincha, Roland P Kuiper, Harry Lesmana and 10 more

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Targeting RUNX1 Germline Variants: Agents Under Investigation.Current hematologic malignancy reports · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Pediatric Cancer Predisposition and Surveillance Update: Summary Perspective and Future Directions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Luke D Maese *University of Utah-Huntsman Cancer Institute, Primary Children's Hospital, Salt Lake City, Utah.ORCID 0000-0002-8739-9100
Marcin W Wlodarski *St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0001-6638-9643
Sun Young KimCincinnati Children's Hospital Medical Center, Cincinnati, Ohio.ORCID 0000-0002-9560-0652
Alison A BertuchDepartment of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0003-1864-8502
Gaelle BougeardUniversité de Rouen Normandie, Inserm U1245 and Rouen University Hospital, Rouen, France.ORCID 0000-0002-1475-0254
Vivian Y ChangUniversity of California Los Angeles, Los Angeles, California.ORCID 0000-0002-4538-1500
Lucy A GodleyDivision of Hematology/Oncology, Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.ORCID 0000-0003-1914-9158
Payal P KhinchaClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0003-2473-7800
Roland P KuiperPrincess Máxima Center for Pediatric Oncology and Department of Genetics, Utrecht University Medical Center, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0003-4928-3809
Harry LesmanaCleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio.ORCID 0000-0001-5496-3839
Rose B McGeeSt. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0001-7392-6515
Lisa J McReynoldsClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0002-1018-1453
Julia MeadeUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-8364-1820
Sharon E PlonDepartment of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-9626-0936
Sharon A SavageClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-6006-0740
Sarah R ScollonDepartment of Pediatrics, Texas Children's Cancer and Hematology Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0003-2017-0245
Hamish S ScottCentre for Cancer Biology, SA Pathology and University of South Australia, Adelaide, South Australia, Australia.ORCID 0000-0002-5813-631X
Michael F WalshMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.ORCID 0000-0001-5006-6778
Kim E Nichols *St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-5581-6555
Christopher C Porter *Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia.ORCID 0000-0001-8774-0180

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Postdoctoral Medical Genetics Training GrantT32GM007471 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI TAO WANG · 1985 to 2026
$8.0M
Pathogenesis of ETV6-Related Acute Lymphoblastic LeukemiaR01CA241452 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI NICHOLS, KIM ERIKA · 2020 to 2025
$2.6M
Dutch KiKa FoundationNational Cancer Institute (NCI)National Institutes of Health (NIH) CA241452NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA241452NIGMS NIH HHS T32 GM007471St. Baldrick's Foundation (SBF)Vera and Joseph Dresner Foundation (Dresner Foundation)
6 · The paper itself

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.

Indexed as

Genetic Predisposition to DiseaseHematologic NeoplasmsChildHematopoietic Stem Cell TransplantationHumansMyelodysplastic SyndromesPractice Guidelines as Topic

Identifiers

PMID39078402
PMCPMC11444884

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.