A tool to predict survival in stage IV entero-pancreatic NEN.
Biomarkers, Tumor
/ analysis
Digestive System Surgical Procedures
/ methods
Female
Gastrointestinal Neoplasms
/ mortality
Humans
Italy
/ epidemiology
Ki-67 Antigen
/ analysis
Male
Middle Aged
Neoplasm Grading
Neoplasm Metastasis
/ pathology
Neoplasm Staging
Neuroendocrine Tumors
/ mortality
Nomograms
Pancreatic Neoplasms
/ mortality
Prognosis
Reproducibility of Results
Survival Analysis
NEP-D
NEP-Score
NEP-T
Neuroendocrine neoplasms
Survival
Journal
Journal of endocrinological investigation
ISSN: 1720-8386
Titre abrégé: J Endocrinol Invest
Pays: Italy
ID NLM: 7806594
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
27
07
2020
accepted:
22
08
2020
pubmed:
7
9
2020
medline:
26
11
2021
entrez:
6
9
2020
Statut:
ppublish
Résumé
Well-differentiated stage IV neuroendocrine neoplasms (NEN) have an extremely heterogeneous, unpredictable clinical behavior. Survival prognostic markers, such as the recently proposed NEP-Score, would be very useful for better defining therapeutic strategies. We aim to verify NEP-Score applicability in an independent cohort of stage IV well-differentiated (WD) gastroentero-pancreatic (GEP) NEN, and identify a derivate prognostic marker taking into account clinical and pathological characteristics at diagnosis. Age, site of primary tumor, primary tumor surgery, symptoms, Ki67, timing of metastases of 27 patients (10 females; mean age at diagnosis 60.2 ± 2.9 years) with stage IV WD GEP NEN were evaluated to calculate the NEP-Score at the end of follow-up (NEP-T). We calculated the NEP-Score at diagnosis (NEP-D), which does not consider the appearance of new metastases during follow-up. Patients were subdivided according to whether they were alive or not at the end of follow-up (EOF) and an NEP-Score threshold was investigated to predict survival. Mean NEP-T and mean NEP-D were significantly lower in 15 live patients as compared to 12 deceased patients (p < 0.01) at EOF. We identified an NEP-D = 116 as the cutoff that significantly predicts survival. No gender differences were identified. In our series, we confirmed NEP-Score applicability. In addition, we propose NEP-D as a simple, quick and cheap prognostic score that can help clinicians in decision making. NEP-D threshold can predict NEN aggressiveness and may be used to define the best personalized therapeutic strategy.
Identifiants
pubmed: 32892316
doi: 10.1007/s40618-020-01404-4
pii: 10.1007/s40618-020-01404-4
pmc: PMC8124053
doi:
Substances chimiques
Biomarkers, Tumor
0
Ki-67 Antigen
0
MKI67 protein, human
0
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
1185-1192Subventions
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca
ID : PRIN 2017Z3N3YC
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