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Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts

BACKGROUND: The Nottinghamshire Lymphoma Registry contains the details of all the patients diagnosed with lymphoma (since 1 January 1973) within a defined geographical area with a population of 1.1 million. It was therefore possible to study the outcome of treatment for Hodgkin’s disease for three 1...

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Autores principales: Bessell, E M, Bouliotis, G, Armstrong, S, Baddeley, J, Haynes, A P, O'Connor, S, Nicholls-Elliott, H, Bradley, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405204/
https://www.ncbi.nlm.nih.gov/pubmed/22713660
http://dx.doi.org/10.1038/bjc.2012.228
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author Bessell, E M
Bouliotis, G
Armstrong, S
Baddeley, J
Haynes, A P
O'Connor, S
Nicholls-Elliott, H
Bradley, M
author_facet Bessell, E M
Bouliotis, G
Armstrong, S
Baddeley, J
Haynes, A P
O'Connor, S
Nicholls-Elliott, H
Bradley, M
author_sort Bessell, E M
collection PubMed
description BACKGROUND: The Nottinghamshire Lymphoma Registry contains the details of all the patients diagnosed with lymphoma (since 1 January 1973) within a defined geographical area with a population of 1.1 million. It was therefore possible to study the outcome of treatment for Hodgkin’s disease for three 10-year cohorts (1973–1982, 1983–1992 and 1993–2002). The aims of the study were to compare survival time among the three patient cohorts, to identify prognostic factors and to estimate relative survival. METHODS: A total of 745 patients diagnosed between 1973 and 2002 were analysed for survival. Survivorship was estimated by the Kaplan-Meier method and parametric survival models. An accelerated failure-time regression was used for multivariate analysis. RESULTS: Overall, patients were observed for 9.8 (0.3–34.82) years (median(range)), on average. One, five and fifteen-year disease-specific survival was found to be 87% (85–90%), 77% (74–80%) and 70% (67–74%), respectively. For those for diagnosed between 1973 and 1982, the 15-year survival was found to be 57% for 1983–1992, it was 74% and for 1993–2002, it was 83% (P<0.001). The difference remained significant after adjusting for prognostic factors. The actuarial risk of developing a second malignancy at 20 years was for the 1973–1982 cohort, 12.4%, and for the 1983–1992 cohort, 18.8%. CONCLUSION: Treatment advances and effective management of toxicities of treatment over time, have resulted in a significantly longer survival for patients with Hodgkin’s disease diagnosed within a defined population.
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spelling pubmed-34052042013-07-24 Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts Bessell, E M Bouliotis, G Armstrong, S Baddeley, J Haynes, A P O'Connor, S Nicholls-Elliott, H Bradley, M Br J Cancer Epidemiology BACKGROUND: The Nottinghamshire Lymphoma Registry contains the details of all the patients diagnosed with lymphoma (since 1 January 1973) within a defined geographical area with a population of 1.1 million. It was therefore possible to study the outcome of treatment for Hodgkin’s disease for three 10-year cohorts (1973–1982, 1983–1992 and 1993–2002). The aims of the study were to compare survival time among the three patient cohorts, to identify prognostic factors and to estimate relative survival. METHODS: A total of 745 patients diagnosed between 1973 and 2002 were analysed for survival. Survivorship was estimated by the Kaplan-Meier method and parametric survival models. An accelerated failure-time regression was used for multivariate analysis. RESULTS: Overall, patients were observed for 9.8 (0.3–34.82) years (median(range)), on average. One, five and fifteen-year disease-specific survival was found to be 87% (85–90%), 77% (74–80%) and 70% (67–74%), respectively. For those for diagnosed between 1973 and 1982, the 15-year survival was found to be 57% for 1983–1992, it was 74% and for 1993–2002, it was 83% (P<0.001). The difference remained significant after adjusting for prognostic factors. The actuarial risk of developing a second malignancy at 20 years was for the 1973–1982 cohort, 12.4%, and for the 1983–1992 cohort, 18.8%. CONCLUSION: Treatment advances and effective management of toxicities of treatment over time, have resulted in a significantly longer survival for patients with Hodgkin’s disease diagnosed within a defined population. Nature Publishing Group 2012-07-24 2012-06-19 /pmc/articles/PMC3405204/ /pubmed/22713660 http://dx.doi.org/10.1038/bjc.2012.228 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Epidemiology
Bessell, E M
Bouliotis, G
Armstrong, S
Baddeley, J
Haynes, A P
O'Connor, S
Nicholls-Elliott, H
Bradley, M
Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title_full Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title_fullStr Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title_full_unstemmed Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title_short Long-term survival after treatment for Hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
title_sort long-term survival after treatment for hodgkin’s disease (1973–2002): improved survival with successive 10-year cohorts
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405204/
https://www.ncbi.nlm.nih.gov/pubmed/22713660
http://dx.doi.org/10.1038/bjc.2012.228
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