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The NIH pediatric/young adult chordoma clinic and natural history study: Making advances in a very rare tumor

  1. Author:
    John, Liny
    Smith, Hannah
    Ilanchezhian, Maran
    Lockridge,Robin
    Reilly, Karlyne M
    Raygada, Margarita
    Dombi, Eva
    Sandler, Abby
    Thomas, Barbara J
    Glod, John
    Miettinen, Markku
    Allen, Taryn
    Sommer, Josh
    Levy, Joan
    Lozinsky, Shannon
    Dix, David
    Bouffet, Eric [ORCID]
    MacDonald, Shannon
    Mukherjee, Debraj
    Snyderman, Carl H
    Rowan, Nicholas R
    Malyapa, Robert
    Park, Deric M
    Heery, Christopher
    Gardner, Paul A
    Cote, Gregory M
    Fuller, Sarah
    Butman, John A
    Jackson, Sadhana
    Gulley, James L
    Widemann, Brigitte C
    Wedekind, Mary Frances
  2. Author Address

    Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA., Clinical Research Directorate (CRD), Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA., Chordoma Foundation, Durham, North Carolina, USA., BC Children 39;s Hospital, Vancouver, British Columbia, Canada., The Hospital for Sick Children, Toronto, Ontario, Canada., Massachusetts General Hospital, Boston, Massachusetts, USA., Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA., University of Maryland Medical Center, Baltimore, Maryland, USA., University of Chicago, Chicago, Illinois, USA., Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA., Radiology and Imaging Sciences, The National Institutes of Health, Bethesda, Maryland, USA., Center for Immuno-Oncology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.,
    1. Year: 2023
    2. Date: Jun 22
    3. Epub Date: 2023 06 22
  1. Journal: Pediatric Blood & Cancer
    1. Pages: e30358
  2. Type of Article: Article
  3. Article Number: e30358
  1. Abstract:

    Chordomas are rare tumors arising from the skull base and spine, with approximately 20 pediatric chordoma cases in the Unitedn States per year. The natural history and optimal treatment of pediatric chordomas, especially poorly differentiated and dedifferentiated subtypes, is incompletely understood. Herein, we present findings from our first National Cancer Institute (NCI) chordoma clinic and a retrospective analysis of published cases of pediatric poorly differentiated chordomas (PDC) and dedifferentiated chordomas (DC). Patients less than 40 years old with chordoma were enrolled on the NCI Natural History and Biospecimens Acquisitions Study for Children and Adults with Rare Solid Tumors protocol (NCT03739827). Chordoma experts reviewed patient records, evaluated patients, and provided treatment recommendations. Patient-reported outcomes, biospecimens, and volumetric tumor analyses were collected. A literature review for pediatric PDC and DC was conducted. Twelve patients (median age: 14 years) attended the clinic, including four patients with active disease and three patients with PDC responsive to systemic therapy. Consensus treatment, management, and recommendations were provided to patients. Literature review returned 45 pediatric cases of PDC or DC with variable treatments and outcomes. A multidisciplinary expert clinic was feasible and successful in improving understanding of pediatric chordoma. While multimodal approaches have all been employed, treatment for PDC has been inconsistent and a recommended standardized treatment approach has not been defined. Centralized efforts, inclusive of specialized chordoma-focused clinics, natural history studies, and prospective analyses will help in the standardization of care for this challenging disease. © 2023 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals LLC. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.

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External Sources

  1. DOI: 10.1002/pbc.30358
  2. PMID: 37347686

Library Notes

  1. Fiscal Year: FY2022-2023
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