The Landscape of US and Global Rare Tumor Research Programs: A Systematic Review.

biospecimens clinical data molecular data rare cancer

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
25 Oct 2023
Historique:
received: 07 08 2023
accepted: 23 09 2023
medline: 25 10 2023
pubmed: 25 10 2023
entrez: 25 10 2023
Statut: aheadofprint

Résumé

Rare cancers and other rare nonmalignant tumors comprise 25% of all cancer diagnoses and account for 25% of all cancer deaths. They are difficult to study due to many factors, including infrequent occurrence, lack of a universal infrastructure for data and/or tissue collection, and a paucity of disease models to test potential treatments. For each individual rare cancer, the limited number of diagnosed cases makes it difficult to recruit sufficient patients for clinical studies, and rare cancer research studies are often siloed. As a result, progress has been slow for many of these cancers. While rare cancer research efforts have increased over time, the breadth of the research landscape is not known. A recent literature search revealed a sharp increase in rare tumor, and rare cancer publications began in the early 2000s. To identify rare cancer research efforts being conducted in the US and globally, we conducted an online search of rare tumor/rare cancer research programs and identified 76 programs. To gain a deeper understanding of these programs, we composed and conducted a survey to ask programs for details about their research efforts. Of the 42 programs contacted to complete the survey, 23 programs responded. Survey results show most programs are collecting clinical data, molecular data, and biospecimens, and many are conducting molecular analyses. This landscape analysis demonstrates that multiple rare cancer research efforts are ongoing, and the rare cancer community may benefit from collaboration among stakeholders to accelerate research and improve patient outcomes.

Identifiants

pubmed: 37878787
pii: 7329715
doi: 10.1093/oncolo/oyad285
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : CCR NIH HHS
Pays : United States
Organisme : NCI NIH HHS
ID : 75N95021D00012
Pays : United States

Informations de copyright

Published by Oxford University Press 2023.

Auteurs

Christina Vivelo (C)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Kelly Government Systems, Bethesda, MD, USA.

Karlyne M Reilly (KM)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Brigitte C Widemann (BC)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Mary Frances Wedekind (MF)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Corrie Painter (C)

Broad Institute, Cambridge, MA, USA.

Allison F O'Neill (AF)

Dana-Farber Cancer Institute/Boston Children's Cancer and Blood Disorders, Center and Harvard Medical School, Department of Pediatric Oncology, Boston, MA, USA.

Sabine Mueller (S)

Department of Neurology, Neurosurgery, and Pediatrics, University of California San Francisco, San Francisco, CA, USA.

Olivier Elemento (O)

Caryl and Israel Englander Institute for Precision Medicine, Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.

Andrea M Gross (AM)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Abby B Sandler (AB)

Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.

Classifications MeSH