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Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study
BACKGROUND AND OBJECTIVES: We tested the hypothesis that overall and cancer-specific survival after a colorectal cancer diagnosis is lower in persons with multiple sclerosis (MS) than in those without MS using a retrospective matched cohort design. METHODS: Using population-based administrative data...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520388/ https://www.ncbi.nlm.nih.gov/pubmed/34526374 http://dx.doi.org/10.1212/WNL.0000000000012634 |
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author | Marrie, Ruth Ann Maxwell, Colleen Mahar, Alyson Ekuma, Okechukwu McClintock, Chad Seitz, Dallasl Groome, Patti |
author_facet | Marrie, Ruth Ann Maxwell, Colleen Mahar, Alyson Ekuma, Okechukwu McClintock, Chad Seitz, Dallasl Groome, Patti |
author_sort | Marrie, Ruth Ann |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: We tested the hypothesis that overall and cancer-specific survival after a colorectal cancer diagnosis is lower in persons with multiple sclerosis (MS) than in those without MS using a retrospective matched cohort design. METHODS: Using population-based administrative data in Manitoba and Ontario, we identified persons with MS from a validated case definition and linked these cohorts to cancer registries to identify those with colorectal cancer. We selected persons with colorectal cancer and without MS, matching 4:1 on birth year, sex, cancer diagnosis year, and region. We used Cox proportional hazards regression to compare all-cause survival between cohorts, adjusting for age at cancer diagnosis, cancer diagnosis year, income, region, and Elixhauser comorbidity score. We compared cancer-specific survival between cohorts using a cause-specific hazards model. We pooled findings across provinces using random-effects meta-analysis. Complementary analyses using a subcohort from Ontario, adjusted for cancer stage and disability status, as measured from the use of home care or long-term care services. RESULTS: We included 338 MS cases and 1,352 controls with colorectal cancer. The mean (SD) age at cancer diagnosis was 64.7 (11.1) years. After adjustment, MS was associated with an increased hazard for all-cause death that was highest 6 months after diagnosis (hazard ratio [HR] 1.45, 95% confidence interval [CI] 1.19–1.76) and then declined over time (HR [95% CI] at 1 year 1.34 [1.09–1.63], 2 years 1.24 [0.99–1.56], 5 years 1.10 [0.80–1.50]). MS was associated with increased cancer-specific death at 6 months after diagnosis only (HR 1.29, 95% CI 1.04–1.61). After adjustment for cancer stage, MS was associated with an increased hazard of death due to any cause (1.60, 95% CI 1.16–2.21) and with cancer-specific death (HR 1.47, 95% CI 1.02–2.12). The association of MS and all-cause death was partially attenuated after adjustment for disability status (HR 1.37, 95% CI 0.97–1.92), as was the association with cancer-specific death (HR 1.34, 95% CI 0.91–1.97). DISCUSSION: Overall and cancer-specific survival was lower in persons with than without MS in the early period after colorectal cancer diagnosis. Further study is warranted to determine what factors underlie these worse outcomes. |
format | Online Article Text |
id | pubmed-8520388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-85203882021-10-18 Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study Marrie, Ruth Ann Maxwell, Colleen Mahar, Alyson Ekuma, Okechukwu McClintock, Chad Seitz, Dallasl Groome, Patti Neurology Research Article BACKGROUND AND OBJECTIVES: We tested the hypothesis that overall and cancer-specific survival after a colorectal cancer diagnosis is lower in persons with multiple sclerosis (MS) than in those without MS using a retrospective matched cohort design. METHODS: Using population-based administrative data in Manitoba and Ontario, we identified persons with MS from a validated case definition and linked these cohorts to cancer registries to identify those with colorectal cancer. We selected persons with colorectal cancer and without MS, matching 4:1 on birth year, sex, cancer diagnosis year, and region. We used Cox proportional hazards regression to compare all-cause survival between cohorts, adjusting for age at cancer diagnosis, cancer diagnosis year, income, region, and Elixhauser comorbidity score. We compared cancer-specific survival between cohorts using a cause-specific hazards model. We pooled findings across provinces using random-effects meta-analysis. Complementary analyses using a subcohort from Ontario, adjusted for cancer stage and disability status, as measured from the use of home care or long-term care services. RESULTS: We included 338 MS cases and 1,352 controls with colorectal cancer. The mean (SD) age at cancer diagnosis was 64.7 (11.1) years. After adjustment, MS was associated with an increased hazard for all-cause death that was highest 6 months after diagnosis (hazard ratio [HR] 1.45, 95% confidence interval [CI] 1.19–1.76) and then declined over time (HR [95% CI] at 1 year 1.34 [1.09–1.63], 2 years 1.24 [0.99–1.56], 5 years 1.10 [0.80–1.50]). MS was associated with increased cancer-specific death at 6 months after diagnosis only (HR 1.29, 95% CI 1.04–1.61). After adjustment for cancer stage, MS was associated with an increased hazard of death due to any cause (1.60, 95% CI 1.16–2.21) and with cancer-specific death (HR 1.47, 95% CI 1.02–2.12). The association of MS and all-cause death was partially attenuated after adjustment for disability status (HR 1.37, 95% CI 0.97–1.92), as was the association with cancer-specific death (HR 1.34, 95% CI 0.91–1.97). DISCUSSION: Overall and cancer-specific survival was lower in persons with than without MS in the early period after colorectal cancer diagnosis. Further study is warranted to determine what factors underlie these worse outcomes. Lippincott Williams & Wilkins 2021-10-05 /pmc/articles/PMC8520388/ /pubmed/34526374 http://dx.doi.org/10.1212/WNL.0000000000012634 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Research Article Marrie, Ruth Ann Maxwell, Colleen Mahar, Alyson Ekuma, Okechukwu McClintock, Chad Seitz, Dallasl Groome, Patti Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title | Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title_full | Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title_fullStr | Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title_full_unstemmed | Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title_short | Colorectal Cancer Survival in Multiple Sclerosis: A Matched Cohort Study |
title_sort | colorectal cancer survival in multiple sclerosis: a matched cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520388/ https://www.ncbi.nlm.nih.gov/pubmed/34526374 http://dx.doi.org/10.1212/WNL.0000000000012634 |
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