Sensitivity and Specificity of the NETest: A Validation Study.


Journal

Neuroendocrinology
ISSN: 1423-0194
Titre abrégé: Neuroendocrinology
Pays: Switzerland
ID NLM: 0035665

Informations de publication

Date de publication:
2021
Historique:
received: 06 05 2020
accepted: 02 07 2020
pubmed: 3 7 2020
medline: 15 1 2022
entrez: 3 7 2020
Statut: ppublish

Résumé

Secretory tumor markers traditionally measured in patients with neuroendocrine tumors (NET) are lacking sensitivity and specificity, and consequently they are of limited clinical utility. The NETest, a novel blood multigene RNA transcript assay, has been found to be highly sensitive and specific. We sought to validate the sensitivity of the NETest in a population of metastatic well-differentiated NETs of gastroenteropancreatic and lung origin and to evaluate NETest specificity in a mixed population of metastatic non-NET gastrointestinal (GI) malignancies and healthy individuals. Forty-nine patients with metastatic NETs, 21 patients with other metastatic GI cancers, and 26 healthy individuals were enrolled in the study. Samples were sent in a blinded fashion to a central laboratory, and an NETest value of 0-13% was considered normal. Using 13% as the upper limit of normal, the sensitivity of the NETest was 98% (95% CI 89-100%). The overall specificity was 66% (95% CI 51-79%), with 16 false-positive results. Specificity was 81% (95% CI 62-92%) among 26 healthy individuals and 48% (95% CI 26-70%) among patients with other GI malignancies. Using an updated normal range of 0-20%, sensitivity was unchanged, but specificity improved to 100% among healthy participants and to 67% among patients with other cancers. The sensitivity of the NETest is exceptionally high (>95%) in a population of metastatic, well-differentiated NETs. Specificity within a healthy population of patients is exceptionally high when using a normal range of 0-20% but relatively low when evaluating patients with other GI malignancies.

Sections du résumé

BACKGROUND
Secretory tumor markers traditionally measured in patients with neuroendocrine tumors (NET) are lacking sensitivity and specificity, and consequently they are of limited clinical utility. The NETest, a novel blood multigene RNA transcript assay, has been found to be highly sensitive and specific. We sought to validate the sensitivity of the NETest in a population of metastatic well-differentiated NETs of gastroenteropancreatic and lung origin and to evaluate NETest specificity in a mixed population of metastatic non-NET gastrointestinal (GI) malignancies and healthy individuals.
DESIGN AND METHODS
Forty-nine patients with metastatic NETs, 21 patients with other metastatic GI cancers, and 26 healthy individuals were enrolled in the study. Samples were sent in a blinded fashion to a central laboratory, and an NETest value of 0-13% was considered normal.
RESULTS
Using 13% as the upper limit of normal, the sensitivity of the NETest was 98% (95% CI 89-100%). The overall specificity was 66% (95% CI 51-79%), with 16 false-positive results. Specificity was 81% (95% CI 62-92%) among 26 healthy individuals and 48% (95% CI 26-70%) among patients with other GI malignancies. Using an updated normal range of 0-20%, sensitivity was unchanged, but specificity improved to 100% among healthy participants and to 67% among patients with other cancers.
CONCLUSIONS
The sensitivity of the NETest is exceptionally high (>95%) in a population of metastatic, well-differentiated NETs. Specificity within a healthy population of patients is exceptionally high when using a normal range of 0-20% but relatively low when evaluating patients with other GI malignancies.

Identifiants

pubmed: 32615553
pii: 000509866
doi: 10.1159/000509866
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

580-585

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Taymeyah Al-Toubah (T)

Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.

Mauro Cives (M)

Department of Biomedical Sciences and Human Oncology, University of Bari, Bari, Italy.

Tiffany Valone (T)

Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.

Kirsten Blue (K)

Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA.

Jonathan Strosberg (J)

Department of Gastrointestinal Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida, USA, jonathan.strosberg@moffitt.org.

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