The implementation of molecular tumor profiling in the practice of pediatric cancer pathology: The pathologists' experience.

Molecular neoplasm pediatric survey

Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
10 Oct 2024
Historique:
revised: 06 09 2024
received: 05 08 2024
accepted: 23 09 2024
medline: 13 10 2024
pubmed: 13 10 2024
entrez: 10 10 2024
Statut: aheadofprint

Résumé

The increased accessibility and utilization of molecular testing including next-generation sequencing (NGS) has impacted the practice of pediatric pathology, with diagnostic, prognostic, and therapeutic implications for our patients. This survey is the first to describe the utilization of molecular testing in the routine practice of pediatric pathology for the care of children with known or suspected solid tumors. The Society for Pediatric Pathology Practice Committee distributed a survey to our membership asking 25 questions about training, practice setting, molecular ordering practices, and barriers to testing. Seventy-five pathologists responded to the survey. The survey provides valuable insight into the current use of molecular testing for the care of children with known or suspected solid tumors. Most respondents reported that they are increasingly using a variety of molecular techniques, with increased use over time, and that NGS is useful. These results highlight a variety of barriers to molecular testing, including cost, insurance coverage, turnaround time, limitations of available assays (including limited coverage of pediatric-specific alterations), and difficulty in determining the most appropriate test to order. These data may be useful in supporting pediatric pathologists in their practice.

Sections du résumé

BACKGROUND BACKGROUND
The increased accessibility and utilization of molecular testing including next-generation sequencing (NGS) has impacted the practice of pediatric pathology, with diagnostic, prognostic, and therapeutic implications for our patients. This survey is the first to describe the utilization of molecular testing in the routine practice of pediatric pathology for the care of children with known or suspected solid tumors.
PROCEDURE METHODS
The Society for Pediatric Pathology Practice Committee distributed a survey to our membership asking 25 questions about training, practice setting, molecular ordering practices, and barriers to testing.
RESULTS RESULTS
Seventy-five pathologists responded to the survey. The survey provides valuable insight into the current use of molecular testing for the care of children with known or suspected solid tumors. Most respondents reported that they are increasingly using a variety of molecular techniques, with increased use over time, and that NGS is useful.
CONCLUSIONS CONCLUSIONS
These results highlight a variety of barriers to molecular testing, including cost, insurance coverage, turnaround time, limitations of available assays (including limited coverage of pediatric-specific alterations), and difficulty in determining the most appropriate test to order. These data may be useful in supporting pediatric pathologists in their practice.

Identifiants

pubmed: 39387390
doi: 10.1002/pbc.31370
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e31370

Informations de copyright

© 2024 Wiley Periodicals LLC.

Références

NCCN. Non‐small cell lung cancer (version 3.2024). Accessed March 31, 2024, https://www.nccn.org/professionals/physician_gls/pdf/nscl.pdf
NCCN. Soft tissue sarcoma (version 3.2023). Accessed March 31, 2024, https://www.nccn.org/professionals/physician_gls/pdf/sarcoma.pdf
NCCN. Neuroblastoma (version 1.2024). Accessed March 31, 2024, https://www.nccn.org/professionals/physician_gls/pdf/neuroblastoma.pdf
Parsons DW, Patton DR, Winter CL, et al. Actionable tumor alterations and treatment protocol enrollment of pediatric and young adult patients with refractory cancers in the National Cancer Institute‐Children's Oncology Group Pediatric MATCH Trial. J Clin Oncol. 2022;40(20):2224‐2234.
Harttrampf AC, Deloger M, Deschamps F, et al. Molecular screening for cancer treatment optimization (MOSCATO‐01) in pediatric patients: a single‐institutional prospective molecular stratification trial. Clin Cancer Res. 2017;23(20):6101‐6112.
Sholler GLS, Bergendahl G, Lewis EC, et al. Molecular‐guided therapy for the treatment of patients with relapsed and refractory childhood cancers: a Beat Childhood Cancer Research Consortium trial. Genome Med. 2024;16(1):28.
Church AJ, Kao PC, Imamovic‐Tuco A, et al. Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer. Nat Med. 2022;28(8):1581‐1589.
Implentation science—opportunities in cancer research. Accessed March 31, 2024, https://www.cancer.gov/research/areas/treatment/implementation‐science
Roberts MC, Spees LP, Freedman AN, et al. Oncologist‐reported reasons for not ordering multimarker tumor panels: results from a nationally representative survey. JCO Precis Oncol. 2021;5. PO.20.00431.
WHO classification of tumours editorial board. Paediatric tumours. 5 ed. vol 7. International Agency for Research on Cancer; 2022.

Auteurs

Catherine K Gestrich (CK)

Department of Pathology, UPMC Children's Hospital of Pittsburgh, Pittsburgh, USA.

Portia Kreiger (P)

Department of Pathology, Children's Hospital of Philadelphia, Philadelphia, USA.

Lea Surrey (L)

Department of Pathology, Children's Hospital of Philadelphia, Philadelphia, USA.

Sherri Besmer (S)

Department of Pathology, SSM Health Cardinal Glennon Children's Hospital, Saint Louis University School of Medicine, St. Louis, Missouri, USA.

Dolores Lopez-Terrada (D)

Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, USA.

Alanna J Church (AJ)

Department of Pathology, Boston Children's Hospital, Boston, USA.

Classifications MeSH