Evidence map›Paper›PMID 39190470›Full record

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

Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group.

Suzanne P MacFarland, Kerri Becktell, Kami Wolfe Schneider, Roland P Kuiper, Harry Lesmana, Julia Meade, Kim E Nichols, Christopher C Porter, Sharon A Savage, Kris Ann Schultz and 9 more

Abstract read
In one paragraph

Article 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 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. 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
  9. Review
  10. Review
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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

19 authors.

Suzanne P MacFarlandChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0001-5894-6403
Kerri BecktellDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0002-1935-5157
Kami Wolfe SchneiderDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado.ORCID 0000-0003-0865-8010
Roland P KuiperPrincess Máxima Center for Pediatric Oncology and Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.ORCID 0000-0003-4928-3809
Harry LesmanaDepartment of Pediatric Hematology, Oncology and BMT, Cleveland Clinic, Cleveland, Ohio.ORCID 0000-0001-5496-3839
Julia MeadeUniversity of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-8364-1820
Kim E NicholsSt. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-5581-6555
Christopher C PorterEmory University & Children's Healthcare of Atlanta, Atlanta, Georgia.ORCID 0000-0001-8774-0180
Sharon A SavageClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.ORCID 0000-0001-6006-0740
Kris Ann SchultzCancer and Blood Disorders, Children's Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-1788-5832
Hamish ScottUniversity of South Australia, Adelaide, Australia.ORCID 0000-0002-5813-631X
Lisa StatesChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0003-0260-3975
Uri TaboriThe Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-5019-2683
Chieko TamuraFMC Tokyo Clinic, Tokyo, Japan.ORCID 0000-0002-7496-4289
Gail TomlinsonUT Health San Antonio, San Antonio, Texas.ORCID 0000-0003-2579-1833
Kristin ZelleyChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0003-0970-1850
Carol DurnoThe Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-2707-2595
Andrew BauerChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-3952-881X
Sharon E PlonTexas Children's Cancer Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-9626-0936

Funding

Detecting DICER1: A global partnership to cure pediatric lung cancerR37CA244940 · NCI · CHILDREN'S HOSPITALS AND CLINICS · PI Kris Ann Pinekenstein Schultz · 2020 to 2026
$2.4M
National Cancer Institute (NCI)National Institutes of Health (NIH) R37CA244940NCI NIH HHS R37 CA244940St. Baldrick's Foundation (SBF)
6 · The paper itself

Abstract

Gastrointestinal (GI) polyposis and cancer in pediatric patients is frequently due to an underlying hereditary cancer risk syndrome requiring ongoing cancer screening. Identification of at-risk patients through family history, clinical features of a syndrome, or symptom onset ensures appropriate cancer risk assessment and management in childhood and beyond. In this 2024 perspective, we outline updates to the hereditary GI cancer screening guidelines first published by the American Association of Cancer Research Pediatric Cancer Predisposition Workshop in 2017. These guidelines consider existing recommendations by pediatric and adult gastroenterology consortia to ensure alignment with gastroenterology practices in managing polyposis conditions. We specifically address the recommendations for pediatric screening in familial adenomatous polyposis, Peutz-Jeghers syndrome, and juvenile polyposis syndrome. Further, we emphasize the importance of multidisciplinary care and partnership with gastroenterology, as it is crucial in management of children and families with these conditions.

Indexed as

Early Detection of CancerGastrointestinal NeoplasmsGenetic Predisposition to DiseaseNeoplastic Syndromes, HereditaryAdenomatous Polyposis ColiChildGenetic TestingHumansPeutz-Jeghers SyndromePractice Guidelines as TopicRisk Assessment

Identifiers

PMID39190470
PMCPMC12826535

What OpenQuestion holds

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Registered trials

None linked

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.