Evidence map›Paper›PMID 18401203›Full record

ArticleJournal of endocrinological investigation2008

Diagnostic and prognostic implications of the World Health Organization classification of neuroendocrine tumors.

A Faggiano, G Mansueto, P Ferolla, F Milone, M L del Basso de Caro, G Lombardi, A Colao, G De Rosa

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Article in Journal of endocrinological investigation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

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21citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Article
  3. Article
  4. Review
  5. Primary renal small cell carcinoma: A case report.World journal of clinical cases · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Primary intracranial neuroendocrine tumor: two case reports.World journal of surgical oncology · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Neuroendocrine tumors (NETs) - experience of a single Center.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

A FaggianoDepartment of Molecular and Clinical Endocrinology and Oncology, Federico II University of Naples, 80131, Naples, Italy. afaggian@unina.it
G Mansueto
P Ferolla
F Milone
M L del Basso de Caro
G Lombardi
A Colao
G De Rosa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuroendocrine differentiation of tumors is often difficult to establish. In the same manner, the evaluation of the prognostic role of neuroendocrine differentiation may constitute a relevant clinical problem. Although different classifications are used for neuroendocrine tumors (NET) of different origin, the last World Health Organization (WHO) classification of NET, originally proposed for gastroenteropancreatic tumors, has proved to be a practical tool to allow pathologists to uniform the diagnoses and re-classify these tumors into 3 main categories.

aimThe present study was carried out in order to evaluate diagnostic and prognostic implications of NET reclassification according to the last WHO classification of NET. MATERIALS AND

methodsThirty-one tumors with an initial diagnosis referable to a NET achieved before 1999 were independently evaluated by 3 pathologists on the basis of the 2000 WHO classification of NET. Immunohistochemistry for panneuroendocrine markers and Ki-67 was also performed in all cases.

resultsTwelve, 14, and 4 tumors were respectively reclassified as well-differentiated NET, well-differentiated neuroendocrine carcinoma and poorly differentiated neuroendocrine carcinoma; 1 tumor was reclassified as mixed endocrine-exocrine tumor. Two or more neuroendocrine markers were expressed in all NET regardless of histotype, differentiation degree, and site of primary tumor. After revision, 10 of the 31 tumors under study (32%) changed histo-prognostic category when compared to the initial diagnosis. Ki-67 score was the best predictor of survival at the multivariate analysis.

conclusionThe WHO classification is suitable to accurately reclassify tumors with an initial diagnosis referable to a NET and to separate these tumors in 3 well-distinct histo-prognostic categories with relevant clinical implications. Ki-67 score seems to be a better predictor of survival than the degree of differentiation.

Indexed as

World Health OrganizationAnalysis of VarianceApudomaCarcinoid TumorCarcinoma, NeuroendocrineCell DifferentiationGastrinomaHumansImmunohistochemistryInsulinomaKi-67 AntigenNeuroendocrine TumorsPrognosisKi-67 Antigen

Identifiers

PMID18401203

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