Literature DB >> 31539715

Epidemiological trends of neuroendocrine tumours over three decades in Queensland, Australia.

David Wyld1, Mark H Wan2, Julie Moore3, Nathan Dunn4, Philippa Youl5.   

Abstract

INTRODUCTION: While neuroendocrine tumours (NETs) account for only a small proportion of cancer diagnoses, incidence has been rising over time. We examined incidence, mortality and survival over three decades in a large population-based registry study.
METHODS: This retrospective study included all cases (n = 4580) of NETs diagnosed from 1986 to 2015 in Queensland, Australia. We examined directly age-standardised incidence and mortality rates. The impact on overall survival according to demographic factors and primary site was modelled using multivariable Cox proportional hazards regression (HR). Cause-specific and relative survival were estimated using the Kaplan-Meier survival function.
RESULTS: Annual incidence increased from 2.0 in 1986 to 6.3 per 100,000 in 2015, while mortality remained stable. The most common primary site was appendix followed by lung, small intestine and rectum. Rectal, stomach, appendiceal and pancreatic NETs had the greatest rate increase, while lung NETs decreased over the same period. Five-year cause-specific survival improved from 69.4% during 1986-1995 to 92.6% from 2006 to 2015. Survival was highest for appendiceal and rectal NETs and lowest for pancreas and unknown primary sites. The risk of dying within five years of diagnosis was about 40% higher for males (HR = 1.41, 95%CI 1.20-1.65) and significantly higher for patients aged over 40 years compared to younger patients (p < 0.001).
CONCLUSION: This study, including 30 years of data, found significantly increasing rates of NETs and confirms results from elsewhere. Increasing survival over time in this study, likely reflects increased awareness, improvements in diagnostic imaging, greater use of endoscopy and colonoscopy, and the development of new therapies.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Incidence; Neuroendocrine neoplasms; Population-based; Survival

Year:  2019        PMID: 31539715     DOI: 10.1016/j.canep.2019.101598

Source DB:  PubMed          Journal:  Cancer Epidemiol        ISSN: 1877-7821            Impact factor:   2.984


  5 in total

Review 1.  How to Select Patients Affected by Neuroendocrine Neoplasms for Surgery.

Authors:  Francesca Fermi; Valentina Andreasi; Francesca Muffatti; Stefano Crippa; Domenico Tamburrino; Stefano Partelli; Massimo Falconi
Journal:  Curr Oncol Rep       Date:  2022-01-25       Impact factor: 5.075

Review 2.  Advances in the Diagnosis and Therapeutic Management of Gastroenteropancreatic Neuroendocrine Neoplasms (GEP-NENs).

Authors:  Krzysztof Kaliszewski; Maksymilian Ludwig; Maria Greniuk; Agnieszka Mikuła; Karol Zagórski; Jerzy Rudnicki
Journal:  Cancers (Basel)       Date:  2022-04-17       Impact factor: 6.575

Review 3.  Update on Epidemiology, Diagnosis, and Biomarkers in Gastroenteropancreatic Neuroendocrine Neoplasms.

Authors:  Daisuke Takayanagi; Hourin Cho; Erika Machida; Atsushi Kawamura; Atsuo Takashima; Satoshi Wada; Takuya Tsunoda; Takashi Kohno; Kouya Shiraishi
Journal:  Cancers (Basel)       Date:  2022-02-22       Impact factor: 6.639

4.  Survival of patients with small bowel neuroendocrine neoplasms in Auckland, Aotearoa New Zealand.

Authors:  Matthew J McGuinness; Braden Woodhouse; Christopher Harmston; Kate Parker; Nicole Kramer; Michael Findlay; Cristin Print; Arend Merrie; Ben Lawrence
Journal:  ANZ J Surg       Date:  2022-06-28       Impact factor: 2.025

5.  Incidence and survival of neuroendocrine neoplasia in England 1995-2018: A retrospective, population-based study.

Authors:  Benjamin E White; Brian Rous; Kandiah Chandrakumaran; Kwok Wong; Catherine Bouvier; Mieke Van Hemelrijck; Gincy George; Beth Russell; Rajaventhan Srirajaskanthan; John K Ramage
Journal:  Lancet Reg Health Eur       Date:  2022-09-23
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.