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An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program

BACKGROUND: There are over 100 histologically distinct types of primary malignant and nonmalignant brain and other central nervous system (CNS) tumors. Our study presents recent trends in the incidence of these tumors using an updated histology recode that incorporates major diagnostic categories li...

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Autores principales: Forjaz, Gonçalo, Barnholtz-Sloan, Jill S, Kruchko, Carol, Siegel, Rebecca, Negoita, Serban, Ostrom, Quinn T, Dickie, Lois, Ruhl, Jennifer, Van Dyke, Alison, Patil, Nirav, Cioffi, Gino, Miller, Kimberly D, Waite, Kristin, Mariotto, Angela B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813198/
https://www.ncbi.nlm.nih.gov/pubmed/33506208
http://dx.doi.org/10.1093/noajnl/vdaa175
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author Forjaz, Gonçalo
Barnholtz-Sloan, Jill S
Kruchko, Carol
Siegel, Rebecca
Negoita, Serban
Ostrom, Quinn T
Dickie, Lois
Ruhl, Jennifer
Van Dyke, Alison
Patil, Nirav
Cioffi, Gino
Miller, Kimberly D
Waite, Kristin
Mariotto, Angela B
author_facet Forjaz, Gonçalo
Barnholtz-Sloan, Jill S
Kruchko, Carol
Siegel, Rebecca
Negoita, Serban
Ostrom, Quinn T
Dickie, Lois
Ruhl, Jennifer
Van Dyke, Alison
Patil, Nirav
Cioffi, Gino
Miller, Kimberly D
Waite, Kristin
Mariotto, Angela B
author_sort Forjaz, Gonçalo
collection PubMed
description BACKGROUND: There are over 100 histologically distinct types of primary malignant and nonmalignant brain and other central nervous system (CNS) tumors. Our study presents recent trends in the incidence of these tumors using an updated histology recode that incorporates major diagnostic categories listed in the 2016 World Health Organization Classification of Tumours of the CNS. METHODS: We used data from the SEER-21 registries for patients of all ages diagnosed in 2000–2017. We calculated age-adjusted incidence rates and fitted a joinpoint regression to the observed data to estimate the Annual Percent Change and 95% confidence intervals over the period 2000–2017. RESULTS: There were 315,184 new malignant (34.2%; 107,890) and nonmalignant (65.8%; 207,294) brain tumor cases during 2004–2017. Nonmalignant meningioma represented 46.5% (146,498) of all brain tumors (malignant and nonmalignant), while glioblastoma represented 50.8% (54,832) of all malignant tumors. Temporal trends were stable or declining except for nonmalignant meningioma (0.7% per year during 2004–2017). Several subtypes presented decreases in trends in the most recent period (2013–2017): diffuse/anaplastic astrocytoma (−1.3% per year, oligodendroglioma (−2.6%), pilocytic astrocytoma (−3.8%), and malignant meningioma (−5.9%). CONCLUSIONS: Declining trends observed in our study may be attributable to recent changes in diagnostic classification and the coding practices stemming from those changes. The recode used in this study enables histology reporting to reflect the changes. It also provides a first step toward the reporting of malignant and nonmalignant brain and other CNS tumors in the Surveillance, Epidemiology, and End Results (SEER) Program by clinically relevant histology groupings.
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spelling pubmed-78131982021-01-26 An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program Forjaz, Gonçalo Barnholtz-Sloan, Jill S Kruchko, Carol Siegel, Rebecca Negoita, Serban Ostrom, Quinn T Dickie, Lois Ruhl, Jennifer Van Dyke, Alison Patil, Nirav Cioffi, Gino Miller, Kimberly D Waite, Kristin Mariotto, Angela B Neurooncol Adv Clinical Investigations BACKGROUND: There are over 100 histologically distinct types of primary malignant and nonmalignant brain and other central nervous system (CNS) tumors. Our study presents recent trends in the incidence of these tumors using an updated histology recode that incorporates major diagnostic categories listed in the 2016 World Health Organization Classification of Tumours of the CNS. METHODS: We used data from the SEER-21 registries for patients of all ages diagnosed in 2000–2017. We calculated age-adjusted incidence rates and fitted a joinpoint regression to the observed data to estimate the Annual Percent Change and 95% confidence intervals over the period 2000–2017. RESULTS: There were 315,184 new malignant (34.2%; 107,890) and nonmalignant (65.8%; 207,294) brain tumor cases during 2004–2017. Nonmalignant meningioma represented 46.5% (146,498) of all brain tumors (malignant and nonmalignant), while glioblastoma represented 50.8% (54,832) of all malignant tumors. Temporal trends were stable or declining except for nonmalignant meningioma (0.7% per year during 2004–2017). Several subtypes presented decreases in trends in the most recent period (2013–2017): diffuse/anaplastic astrocytoma (−1.3% per year, oligodendroglioma (−2.6%), pilocytic astrocytoma (−3.8%), and malignant meningioma (−5.9%). CONCLUSIONS: Declining trends observed in our study may be attributable to recent changes in diagnostic classification and the coding practices stemming from those changes. The recode used in this study enables histology reporting to reflect the changes. It also provides a first step toward the reporting of malignant and nonmalignant brain and other CNS tumors in the Surveillance, Epidemiology, and End Results (SEER) Program by clinically relevant histology groupings. Oxford University Press 2020-12-08 /pmc/articles/PMC7813198/ /pubmed/33506208 http://dx.doi.org/10.1093/noajnl/vdaa175 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Forjaz, Gonçalo
Barnholtz-Sloan, Jill S
Kruchko, Carol
Siegel, Rebecca
Negoita, Serban
Ostrom, Quinn T
Dickie, Lois
Ruhl, Jennifer
Van Dyke, Alison
Patil, Nirav
Cioffi, Gino
Miller, Kimberly D
Waite, Kristin
Mariotto, Angela B
An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title_full An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title_fullStr An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title_full_unstemmed An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title_short An updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the Surveillance, Epidemiology, and End Results Program
title_sort updated histology recode for the analysis of primary malignant and nonmalignant brain and other central nervous system tumors in the surveillance, epidemiology, and end results program
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813198/
https://www.ncbi.nlm.nih.gov/pubmed/33506208
http://dx.doi.org/10.1093/noajnl/vdaa175
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