Risk stratification of gastrointestinal stromal tumors by Nanostring gene expression profiling.


Journal

Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 05 10 2021
accepted: 12 01 2022
pubmed: 29 1 2022
medline: 20 5 2022
entrez: 28 1 2022
Statut: ppublish

Résumé

The risk assessment classification schemes for gastrointestinal stromal tumors (GIST) include tumor site, size, mitotic count and variably tumor rupture. Heterogeneity in high-risk GIST poses limitations for current classification schemes. This study aims to demonstrate the clinical utility of risk stratification by gene expression profiling (GEP) using Nanostring technology. Fifty-six GIST cases were analyzed using a 231 gene expression panel. GEP results were correlated with clinical and pathological data. The prognostic performance was assessed in 34 patients with available survival data using ROC curves, Kaplan-Meier survival curves and compared with traditional risk assessment schemes. Volcano plot analysis identified seven genes with significantly higher expression (FDR < .0.05) in high-risk than in non-high-risk tumors, namely TYMS, CDC2, TOP2A, CCNA2, E2F1, PCNA, and BIRC5. Together, these transcripts exhibited significantly higher expression in high-risk tumors than in intermediate (P < 0.01), low (P < 0.001), and very low (P = 0.01) risk tumors. Receiver-operating characteristic curve analysis demonstrated area under the curve (AUC) to be 0.858 for the separation of high-risk and non-high-risk tumors. Kaplan-Meier survival analysis demonstrated improved risk stratification (log-rank test P < 0.001) compared to the current risk assessment classification (P = 0.231). In addition to current clinical and histology-based risk classification for patients with GIST, gene expression may offer complementary prognostic information.

Identifiants

pubmed: 35089395
doi: 10.1007/s00432-022-03924-3
pii: 10.1007/s00432-022-03924-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1325-1336

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Klaudia Nowak (K)

Department of Laboratory Medicine and Pathology, University of Alberta, 8440 112 Street NW, Edmonton, AB, T6G 2B7, Canada.

Kim Formenti (K)

Department of Laboratory Medicine and Pathology, University of Alberta, 8440 112 Street NW, Edmonton, AB, T6G 2B7, Canada.

Jingyang Huang (J)

Department of Laboratory Medicine and Pathology, University of Alberta, 8440 112 Street NW, Edmonton, AB, T6G 2B7, Canada.

Gilbert Bigras (G)

Department of Laboratory Medicine and Pathology, University of Alberta and Cross Cancer Institute, 11560 University Avenue, Edmonton, AB, T6G 1Z2, Canada.

Quincy Chu (Q)

Department of Oncology, University of Alberta and Cross Cancer Institute, 11560 University Avenue, Edmonton, AB, T6G 1Z2, Canada.

Benjamin A Adam (BA)

Department of Laboratory Medicine and Pathology, University of Alberta, 8440 112 Street NW, Edmonton, AB, T6G 2B7, Canada.

Iyare Izevbaye (I)

Department of Laboratory Medicine and Pathology, University of Alberta, 8440 112 Street NW, Edmonton, AB, T6G 2B7, Canada. izevbaye@ualberta.ca.

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