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Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry
OBJECTIVE: Our aim was to describe and compare self-reported causal attributions (interpretations of what caused an illness) among cancer survivors and to assess which sociodemographic and clinical characteristics are associated with them. METHODS: Data from five population-based PROFILES registry s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971112/ https://www.ncbi.nlm.nih.gov/pubmed/33644846 http://dx.doi.org/10.1007/s11764-021-00989-w |
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author | Vlooswijk, Carla Husson, Olga Oerlemans, Simone Ezendam, Nicole Schoormans, Dounya de Rooij, Belle Mols, Floortje |
author_facet | Vlooswijk, Carla Husson, Olga Oerlemans, Simone Ezendam, Nicole Schoormans, Dounya de Rooij, Belle Mols, Floortje |
author_sort | Vlooswijk, Carla |
collection | PubMed |
description | OBJECTIVE: Our aim was to describe and compare self-reported causal attributions (interpretations of what caused an illness) among cancer survivors and to assess which sociodemographic and clinical characteristics are associated with them. METHODS: Data from five population-based PROFILES registry samples (i.e. lymphoma (n = 993), multiple myeloma (n = 156), colorectal (n = 3989), thyroid (n = 306), endometrial (n = 741), prostate cancer (n = 696)) were used. Causal attributions were assessed with a single question. RESULTS: The five most often reported causal attributions combined were unknown (21%), lifestyle (19%), biological (16%), other (14%), and stress (12%). Lymphoma (49%), multiple myeloma (64%), thyroid (55%), and prostate (64%) cancer patients mentioned fixed causes far more often than modifiable or modifiable/fixed. Colorectal (33%, 34%, and 33%) and endometrial (38%, 32%, and 30%) cancer survivors mentioned causes that were fixed, modifiable, or both almost equally often. Colorectal, endometrial, and prostate cancer survivors reported internal causes most often, whereas multiple myeloma survivors more often reported external causes, while lymphoma and thyroid cancer survivors had almost similar rates of internal and external causes. Females, those older, those treated with hormonal therapy, and those diagnosed with prostate cancer were less likely to identify modifiable causes while those diagnosed with stage 2, singles, with ≥2 comorbid conditions, and those with endometrial cancer were more likely to identify modifiable causes. CONCLUSION: In conclusion, this study showed that patients report both internal and external causes of their illness and both fixed and modifiable causes. This differsbetween the various cancer types. IMPLICATIONS FOR CANCER SURVIVORS: Although the exact cause of cancer in individual patients is often unknown, having a well-informed perception of the modifiable causes of one’s cancer is valuable since it can possibly help survivors with making behavioural adjustments in cases where this is necessary or possible. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11764-021-00989-w. |
format | Online Article Text |
id | pubmed-9971112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-99711122023-03-01 Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry Vlooswijk, Carla Husson, Olga Oerlemans, Simone Ezendam, Nicole Schoormans, Dounya de Rooij, Belle Mols, Floortje J Cancer Surviv Article OBJECTIVE: Our aim was to describe and compare self-reported causal attributions (interpretations of what caused an illness) among cancer survivors and to assess which sociodemographic and clinical characteristics are associated with them. METHODS: Data from five population-based PROFILES registry samples (i.e. lymphoma (n = 993), multiple myeloma (n = 156), colorectal (n = 3989), thyroid (n = 306), endometrial (n = 741), prostate cancer (n = 696)) were used. Causal attributions were assessed with a single question. RESULTS: The five most often reported causal attributions combined were unknown (21%), lifestyle (19%), biological (16%), other (14%), and stress (12%). Lymphoma (49%), multiple myeloma (64%), thyroid (55%), and prostate (64%) cancer patients mentioned fixed causes far more often than modifiable or modifiable/fixed. Colorectal (33%, 34%, and 33%) and endometrial (38%, 32%, and 30%) cancer survivors mentioned causes that were fixed, modifiable, or both almost equally often. Colorectal, endometrial, and prostate cancer survivors reported internal causes most often, whereas multiple myeloma survivors more often reported external causes, while lymphoma and thyroid cancer survivors had almost similar rates of internal and external causes. Females, those older, those treated with hormonal therapy, and those diagnosed with prostate cancer were less likely to identify modifiable causes while those diagnosed with stage 2, singles, with ≥2 comorbid conditions, and those with endometrial cancer were more likely to identify modifiable causes. CONCLUSION: In conclusion, this study showed that patients report both internal and external causes of their illness and both fixed and modifiable causes. This differsbetween the various cancer types. IMPLICATIONS FOR CANCER SURVIVORS: Although the exact cause of cancer in individual patients is often unknown, having a well-informed perception of the modifiable causes of one’s cancer is valuable since it can possibly help survivors with making behavioural adjustments in cases where this is necessary or possible. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11764-021-00989-w. Springer US 2021-03-01 2023 /pmc/articles/PMC9971112/ /pubmed/33644846 http://dx.doi.org/10.1007/s11764-021-00989-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vlooswijk, Carla Husson, Olga Oerlemans, Simone Ezendam, Nicole Schoormans, Dounya de Rooij, Belle Mols, Floortje Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title | Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title_full | Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title_fullStr | Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title_full_unstemmed | Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title_short | Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry |
title_sort | self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the profiles registry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971112/ https://www.ncbi.nlm.nih.gov/pubmed/33644846 http://dx.doi.org/10.1007/s11764-021-00989-w |
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