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Demographic, clinical, and pathological features of early onset pancreatic cancer patients

BACKGROUND: Early onset pancreatic cancer (EOPC), i.e. pancreatic ductal adenocarcinoma (PDAC) occurring in patients below 50 years of age, is rare and there is limited information regarding risk factors, molecular basis and outcome. This study aimed to determine the demographic and clinicopathologi...

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Autores principales: Ntala, Chara, Debernardi, Silvana, Feakins, Roger M., Crnogorac-Jurcevic, Tatjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136158/
https://www.ncbi.nlm.nih.gov/pubmed/30208959
http://dx.doi.org/10.1186/s12876-018-0866-z
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author Ntala, Chara
Debernardi, Silvana
Feakins, Roger M.
Crnogorac-Jurcevic, Tatjana
author_facet Ntala, Chara
Debernardi, Silvana
Feakins, Roger M.
Crnogorac-Jurcevic, Tatjana
author_sort Ntala, Chara
collection PubMed
description BACKGROUND: Early onset pancreatic cancer (EOPC), i.e. pancreatic ductal adenocarcinoma (PDAC) occurring in patients below 50 years of age, is rare and there is limited information regarding risk factors, molecular basis and outcome. This study aimed to determine the demographic and clinicopathological features and survival figures for EOPC. METHODS: A retrospective analysis of patients treated at the Royal London Hospital for PDAC between September 2004 and September 2015 was performed. Data on demographics, risk factors, presentation, pathological features, treatment and survival outcome were compared in EOPC and older PDAC patients. RESULTS: Of 369 PDAC cases identified, 35 (9.5%) were EOPC. Compared to older patients, EOPC patients were more frequently male (71% vs 54%, p = 0.043) and less commonly of British origin (37% vs 70%, p = 0.002). There was no significant difference regarding the prevalence of any of the risk factors known to be associated with older PDAC patients. Fewer EOPC patients presented with resectable disease (23% vs 44%, p = 0.015) and more received adjuvant chemo/radiotherapy (60% vs 46%, p = 0.008). The overall median survival and stage specific survival did not differ significantly between the two groups, although a longer survival for localized disease was seen in EOPC patients (25 months (12.9–37, 95%CI) vs 13 months (10.5–15.5 95%CI) for older PDAC patients). CONCLUSIONS: The EOPC patients had different demographics and were more likely than their older PDAC counterparts to be male. Typically they presented with more advanced disease, received more aggressive treatment, and had on overall similar survival outcome.
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spelling pubmed-61361582018-09-15 Demographic, clinical, and pathological features of early onset pancreatic cancer patients Ntala, Chara Debernardi, Silvana Feakins, Roger M. Crnogorac-Jurcevic, Tatjana BMC Gastroenterol Research Article BACKGROUND: Early onset pancreatic cancer (EOPC), i.e. pancreatic ductal adenocarcinoma (PDAC) occurring in patients below 50 years of age, is rare and there is limited information regarding risk factors, molecular basis and outcome. This study aimed to determine the demographic and clinicopathological features and survival figures for EOPC. METHODS: A retrospective analysis of patients treated at the Royal London Hospital for PDAC between September 2004 and September 2015 was performed. Data on demographics, risk factors, presentation, pathological features, treatment and survival outcome were compared in EOPC and older PDAC patients. RESULTS: Of 369 PDAC cases identified, 35 (9.5%) were EOPC. Compared to older patients, EOPC patients were more frequently male (71% vs 54%, p = 0.043) and less commonly of British origin (37% vs 70%, p = 0.002). There was no significant difference regarding the prevalence of any of the risk factors known to be associated with older PDAC patients. Fewer EOPC patients presented with resectable disease (23% vs 44%, p = 0.015) and more received adjuvant chemo/radiotherapy (60% vs 46%, p = 0.008). The overall median survival and stage specific survival did not differ significantly between the two groups, although a longer survival for localized disease was seen in EOPC patients (25 months (12.9–37, 95%CI) vs 13 months (10.5–15.5 95%CI) for older PDAC patients). CONCLUSIONS: The EOPC patients had different demographics and were more likely than their older PDAC counterparts to be male. Typically they presented with more advanced disease, received more aggressive treatment, and had on overall similar survival outcome. BioMed Central 2018-09-12 /pmc/articles/PMC6136158/ /pubmed/30208959 http://dx.doi.org/10.1186/s12876-018-0866-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ntala, Chara
Debernardi, Silvana
Feakins, Roger M.
Crnogorac-Jurcevic, Tatjana
Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title_full Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title_fullStr Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title_full_unstemmed Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title_short Demographic, clinical, and pathological features of early onset pancreatic cancer patients
title_sort demographic, clinical, and pathological features of early onset pancreatic cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136158/
https://www.ncbi.nlm.nih.gov/pubmed/30208959
http://dx.doi.org/10.1186/s12876-018-0866-z
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