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Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study
Objective To determine whether modern treatments for cancer are associated with a net increased or decreased risk of death from neoplastic and non-neoplastic causes among survivors of childhood cancer. Design Population based cohort study. Setting British Childhood Cancer Survivor Study. Participant...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008696/ https://www.ncbi.nlm.nih.gov/pubmed/27586237 http://dx.doi.org/10.1136/bmj.i4351 |
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author | Fidler, Miranda M Reulen, Raoul C Winter, David L Kelly, Julie Jenkinson, Helen C Skinner, Rod Frobisher, Clare Hawkins, Michael M |
author_facet | Fidler, Miranda M Reulen, Raoul C Winter, David L Kelly, Julie Jenkinson, Helen C Skinner, Rod Frobisher, Clare Hawkins, Michael M |
author_sort | Fidler, Miranda M |
collection | PubMed |
description | Objective To determine whether modern treatments for cancer are associated with a net increased or decreased risk of death from neoplastic and non-neoplastic causes among survivors of childhood cancer. Design Population based cohort study. Setting British Childhood Cancer Survivor Study. Participants Nationwide population based cohort of 34 489 five year survivors of childhood cancer with a diagnosis from 1940 to 2006 and followed up until 28 February 2014. Main outcome measures Cause specific standardised mortality ratios and absolute excess risks are reported. Multivariable Poisson regression models were utilised to evaluate the simultaneous effect of risk factors. Likelihood ratio tests were used to test for heterogeneity or trend. Results Overall, 4475 deaths were observed, which was 9.1 (95% confidence interval 8.9 to 9.4) times that expected in the general population, corresponding to 64.2 (95% confidence interval 62.1 to 66.3) excess deaths per 10 000 person years. The number of excess deaths from all causes declined among those treated more recently; those treated during 1990-2006 experienced 30% of the excess number of deaths experienced by those treated before 1970. The corresponding percentages for the decline in excess deaths from recurrence or progression and non-neoplastic causes were 30% and 60%, respectively. Among survivors aged 50-59 years, 41% and 22% of excess deaths were attributable to subsequent primary neoplasms and circulatory conditions, respectively, whereas the corresponding percentages among those aged 60 years or more were 31% and 37%. Conclusions The net effects of changes in cancer treatments, and surveillance and management for late effects, over the period 1940 to 2006 was to reduce the excess number of deaths from both recurrence or progression and non-neoplastic causes among those treated more recently. Among survivors aged 60 years or more, the excess number of deaths from circulatory causes exceeds the excess number of deaths from subsequent primary neoplasms. The important message for the evidence based surveillance aimed at preventing excess mortality and morbidity in survivors aged 60 years or more is that circulatory disease overtakes subsequent primary neoplasms as the leading cause of excess mortality. |
format | Online Article Text |
id | pubmed-5008696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50086962016-09-02 Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study Fidler, Miranda M Reulen, Raoul C Winter, David L Kelly, Julie Jenkinson, Helen C Skinner, Rod Frobisher, Clare Hawkins, Michael M BMJ Research Objective To determine whether modern treatments for cancer are associated with a net increased or decreased risk of death from neoplastic and non-neoplastic causes among survivors of childhood cancer. Design Population based cohort study. Setting British Childhood Cancer Survivor Study. Participants Nationwide population based cohort of 34 489 five year survivors of childhood cancer with a diagnosis from 1940 to 2006 and followed up until 28 February 2014. Main outcome measures Cause specific standardised mortality ratios and absolute excess risks are reported. Multivariable Poisson regression models were utilised to evaluate the simultaneous effect of risk factors. Likelihood ratio tests were used to test for heterogeneity or trend. Results Overall, 4475 deaths were observed, which was 9.1 (95% confidence interval 8.9 to 9.4) times that expected in the general population, corresponding to 64.2 (95% confidence interval 62.1 to 66.3) excess deaths per 10 000 person years. The number of excess deaths from all causes declined among those treated more recently; those treated during 1990-2006 experienced 30% of the excess number of deaths experienced by those treated before 1970. The corresponding percentages for the decline in excess deaths from recurrence or progression and non-neoplastic causes were 30% and 60%, respectively. Among survivors aged 50-59 years, 41% and 22% of excess deaths were attributable to subsequent primary neoplasms and circulatory conditions, respectively, whereas the corresponding percentages among those aged 60 years or more were 31% and 37%. Conclusions The net effects of changes in cancer treatments, and surveillance and management for late effects, over the period 1940 to 2006 was to reduce the excess number of deaths from both recurrence or progression and non-neoplastic causes among those treated more recently. Among survivors aged 60 years or more, the excess number of deaths from circulatory causes exceeds the excess number of deaths from subsequent primary neoplasms. The important message for the evidence based surveillance aimed at preventing excess mortality and morbidity in survivors aged 60 years or more is that circulatory disease overtakes subsequent primary neoplasms as the leading cause of excess mortality. BMJ Publishing Group Ltd. 2016-09-01 /pmc/articles/PMC5008696/ /pubmed/27586237 http://dx.doi.org/10.1136/bmj.i4351 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/3.0/. |
spellingShingle | Research Fidler, Miranda M Reulen, Raoul C Winter, David L Kelly, Julie Jenkinson, Helen C Skinner, Rod Frobisher, Clare Hawkins, Michael M Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title | Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title_full | Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title_fullStr | Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title_full_unstemmed | Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title_short | Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study |
title_sort | long term cause specific mortality among 34 489 five year survivors of childhood cancer in great britain: population based cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008696/ https://www.ncbi.nlm.nih.gov/pubmed/27586237 http://dx.doi.org/10.1136/bmj.i4351 |
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