Increased incidence trend of low-grade and high-grade neuroendocrine neoplasms
- PMID: 28303513
- PMCID: PMC5671554
- DOI: 10.1007/s12020-017-1273-x
Increased incidence trend of low-grade and high-grade neuroendocrine neoplasms
Abstract
Purpose: The incidence of neuroendocrine neoplasms is increasing. This work aimed at: (i) establishing worldwide incidence trend of low-grade neuroendocrine neoplasms; (ii) defining the incidence and temporal trend of high-grade neuroendocrine neoplasms in USA utilizing the Surveillance Epidemiology and End Results database; (iii) comparing trends for low-grade vs. high-grade neuroendocrine neoplasms.
Methods: We conducted a literature search on MEDLINE and Scopus databases and incidence trends were plotted for 1973-2012. The Surveillance Epidemiology and End Results database was used to identify incidence rates in USA for 1973-2012. Incidence rates were stratified according to histological grade, gender and ethnicity. Trends were summarized as annual percent change and corresponding 95% confidence interval.
Results: 11 studies were identified involving 72,048 cases; neuroendocrine neoplasm incidence rates increased over time in all countries for all sites, except for appendix. In Surveillance Epidemiology and End Results low-grade neuroendocrine neoplasm incidence rate increased from 1.09 in 1973 to 3.51 per 100,000 in 2012. During this interval, high-grade neuroendocrine neoplasm incidence rate increased from 2.54 to 10.52 per 100,000. African Americans had the highest rates of digestive neuroendocrine neoplasms with male prevalence in high-grade.
Conclusions: Our data indicate an increase in the incidence of neuroendocrine neoplasms as a worldwide phenomenon, affecting most anatomical sites and involving both low-grade and high-grade neoplasms.
Keywords: Cancer; High-grade; Incidence; Low-grade; Neuroendocrine.
Conflict of interest statement
The authors declare that they have no competing interests.
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References
-
- Inzani F, Rindi G. Classification of Neuroendocrine Neoplasms. In: Pacak K, Taïeb D, editors. Diagnostic and Therapeutic Nuclear Medicine for Neuroendocrine Tumors. Contemporary Endocrinology. Cham: Springer; 2017. pp. 1–14.
-
- Rindi G, Arnold R, Capella C, Klimstra DS, Klöppel G, Komminoth P, Solcia E. Nomenclature and classification of digestive neuroendocrine tumours. In: Bosman F, Carneiro F, editors. World Health Organization Classification of Tumours, Pathology and Genetics of Tumours of the Digestive System. Lyon: IARC; 2010. pp. 10–12.
-
- Milione M, Maisonneuve P, Spada F, Pellegrinelli A, Spaggiari P, Albarello L, Pisa E, Barberis M, Vanoli A, Buzzoni R, Pusceddu S, Concas L, Sessa F, Solcia E, Capella C, Fazio N, La Rosa S. The clinicopathologic heterogeneity of grade 3 gastroenteropancreatic neuroendocrine neoplasms: morphological differentiation and proliferation identify different prognostic categories. Neuroendocrinology. 2017;104(1):85–93. doi: 10.1159/000445165. - DOI - PubMed
-
- M.B. Amin, S.B. Edge, F.L. Greene, D.R. Byrd, D.B. Brookland, M.K. Washington, J.E. Gershenwald, C.C. Compton, K.R. Hess, D.C. Sullivan, J.M. Jessup, J.D. Brierley, L.E. Gaspar, R.L. Schilsky, C.M. Balch, D.P. Winchester, E.A. Asare, M. Madera, D.M. Gress, L.R. Meyer (eds.), AJCC Cancer Staging. Manual, 8th ed. (Springer, New York, Philadelphia, 2017)
-
- E.A. Woltering, E.K. Bergsland, D.T. Beyer, T.M. O’Dorisio, G. Rindi, D.S. Klimstra, L.H. Tang, D. Reidy-Lagunes, J.R. Strosberg, E.M. Wolin, A.I. Vinik, E.K. Nakakura, E.A. Asare, D.L. Bushnell, R.L. Schilsky, Y.-Z. Wang, M.K. Kim, E.H. Liu, R.T. Jensen, R.K.S. Wong, J.K. Ramage, K. Mallin, R.F. Pommier: Neuroendocrine tumors of the jejunum and ileum. In: M.B. Amin, S.B. Edge, F.L. Greene, D.R. Byrd, D.B. Brookland, M.K. Washington, J.E. Gershenwald, C.C. Compton, K.R. Hess, D.C. Sullivan, J.M. Jessup, J.D. Brierley, L.E. Gaspar, R.L. Schilsky, C.M. Balch, D.P. Winchester, E.A. Asare, M. Madera, D.M. Gress, L.R. Meyer (eds.) AJCC Cancer Staging Manual. (Springer, New York, Philadelphia, 2017), pp. 375–387
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